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The human skeleton (Lewis).

The human skeleton (Lewis).


STRUCTURE AND FUNCTIONS
of
THE BODY

A HAND-BOOK OF ANATOMY AND PHYSIOLOGY FOR
NURSES AND OTHERS DESIRING A PRACTICAL
KNOWLEDGE OF THE SUBJECT

A HANDBOOK OF ANATOMY AND PHYSIOLOGY FOR
NURSES AND OTHERS SEEKING PRACTICAL
KNOWLEDGE OF THE TOPIC

BY
ANNETTE FISKE, A. M.
GRADUATE OF THE WALTHAM TRAINING SCHOOL FOR NURSES

BY
ANNETTE FISKE, M.A.
GRADUATE OF THE WALTHAM TRAINING SCHOOL FOR NURSES

ILLUSTRATED

Illustrated

PHILADELPHIA AND LONDON
W. B. SAUNDERS COMPANY
1911

PHILADELPHIA AND LONDON
W. B. SAUNDERS COMPANY
1911


Copyright, 1911, by W. B. Saunders Company
PRINTED IN AMERICA

Copyright, 1911, by W. B. Saunders Company
PRINTED IN AMERICA


PRESS OF
W. B. SAUNDERS COMPANY
PHILADELPHIA

PRESS OF
W. B. SAUNDERS COMPANY
PHILADELPHIA


TO MY FATHER

TO DAD

and

and

TO DR. ALFRED WORCESTER

To Dr. Alfred Worcester

as those who have perhaps most helped me in
the formation and realization of my ideals
this book is affectionately dedicated

as those who have likely contributed the most to
the formation and realization of my ideals
this book is warmly dedicated


PREFACE.

Although there are already in existence many books on anatomy and physiology for nurses, none with which I am acquainted has seemed to me to provide in concise form just the knowledge needed by the nurse in her profession. Most of them, moreover, separate the anatomy from the physiology and all treat the different systems of tissues separately, first the bones, then the muscles, and so on. These defects, as they seem to me, I have attempted to correct not only by weaving the physiology in with the anatomy, but by treating first the general structures found throughout the body and then describing the structure and function of each part in detail. Thus, the first chapter is devoted to a description of the general structure of all the tissues, a separate chapter being devoted, however, to the skin, its appendages, and function, including the sense of touch. Then the head with its bones, muscles, and organs of special sense is described, while the brain is treated with the rest of the nervous system, thus forming the connecting link between the head and the body. In the same way the back, chest, abdomen, pelvis, and extremities are taken up in turn and the bones, muscles, blood-vessels, nerves, and special organs of each, together with their functions, described.

Although there are already many books on anatomy and physiology for nurses, none that I know of seem to provide the concise knowledge needed by nurses in their profession. Most of them separate anatomy from physiology, and they treat the different systems of tissues one by one—first the bones, then the muscles, and so on. I’ve tried to fix these issues by combining physiology with anatomy, starting with general structures found throughout the body and then detailing the structure and function of each part. So, the first chapter focuses on the general structure of all the tissues, with a separate chapter dedicated to the skin, its appendages, and its functions, including the sense of touch. Next, the head is described along with its bones, muscles, and special sensory organs, while the brain is discussed along with the rest of the nervous system, creating a link between the head and the body. Similarly, the back, chest, abdomen, pelvis, and limbs are discussed in turn, detailing the bones, muscles, blood vessels, nerves, and special organs of each, along with their functions.

Although written more particularly for nurses I am in hopes that this book may prove useful to any others who may desire to acquire a practical knowledge of anatomy and physiology.

Although this book is primarily written for nurses, I hope it will also be helpful to anyone else who wants to gain practical knowledge of anatomy and physiology.

Besides the usual text-books, I am much indebted for material to notes [Pg 6] taken in lecture courses given by Dr. Fred R. Jouett and Dr. F. J. Goodridge of Cambridge, Mass., at the Cambridge School of Nursing, and by Dr. Vivian Daniel of Watertown at the Waltham Training School for Nurses.

Besides the usual textbooks, I owe a lot of my material to notes [Pg 6] I took during lectures by Dr. Fred R. Jouett and Dr. F. J. Goodridge from Cambridge, Mass., at the Cambridge School of Nursing, and by Dr. Vivian Daniel from Watertown at the Waltham Training School for Nurses.

I wish particularly to express my gratitude and appreciation for the kind and helpful criticism given me by Dr. Eugene A. Darling, Assistant Professor of Physiology, Harvard College.

I especially want to express my gratitude and appreciation for the kind and helpful feedback I received from Dr. Eugene A. Darling, Assistant Professor of Physiology at Harvard College.

Annette Fiske.

Annette Fiske.

May, 1911.

May 1911.


CONTENTS.

CHAPTER I.
PAGE
Composition and Overall Structure of the Body 11

Chemical Constitution of the Body, 11—The Cell, 12—The Fundamental Tissues of the Body, 13—Epithelial Tissue, 14—Connective Tissue, 15—Structure of Bone, 17—Bone Formation, 18—Chemical Composition of Bone, 18—Classification and Function of Bones, 19—Joints, 20—Muscle, 21—Action of the Muscles, 23—Physiology of Muscle, 24—Cilia, 27—The Blood, 27—Arteries, 27—Veins, 28—Capillaries, 28—Lymphatic System, 29—Lymphatic Vessels, 31—Lymphatic Glands, 32—Lymph, 32—Glands, 35—Ductless Glands, 36—Nervous Tissue, 36.

Chemical Constitution of the Body, 11—The Cell, 12—The Fundamental Tissues of the Body, 13—Epithelial Tissue, 14—Connective Tissue, 15—Structure of Bone, 17—Bone Formation, 18—Chemical Composition of Bone, 18—Classification and Function of Bones, 19—Joints, 20—Muscle, 21—Action of the Muscles, 23—Physiology of Muscle, 24—Cilia, 27—The Blood, 27—Arteries, 27—Veins, 28—Capillaries, 28—Lymphatic System, 29—Lymphatic Vessels, 31—Lymphatic Glands, 32—Lymph, 32—Glands, 35—Ductless Glands, 36—Nervous Tissue, 36.

CHAPTER II.
The Skin, Its Appendages, and Its Function 39

The Skin, 39—Appendages of the Skin: Nails, 40—Hair, 40—Sebaceous Glands, 41—Sweat Glands, 42—Sweat, 42—Temperature Regulation, 43—Fever, 45—Sense of Touch, 45—Touch Corpuscles, 46.

The Skin, 39—Skin Appendages: Nails, 40—Hair, 40—Sebaceous Glands, 41—Sweat Glands, 42—Sweat, 42—Temperature Regulation, 43—Fever, 45—Sense of Touch, 45—Touch Receptors, 46.

CHAPTER III.
The Skull and Face 48

The Cranial Bones, 48—Frontal Bone, 49—Parietal Bones, 49—Occipital Bone, 50—Occipito-frontalis Muscle, 51—Temporal Bones, 51—Sphenoid or Wedge Bone, 52—Ethmoid Bone, 53—Turbinated Bones, 53—Ossification of Sutures, 53—Bones of the Face, 53—Superior Maxillary Bones, 54—Antrum of Highmore, 54—Malar or Cheek Bones, 54—Lachrymal Bones, 54—Palate Bones, 54—Nasal Bones, 55—Vomer, 55—Inferior Turbinated Bones, 55—Inferior Maxillary Bone or Lower Jaw, 55—Sublingual Gland, 56—Submaxillary Gland, 56.

The Cranial Bones, 48—Frontal Bone, 49—Parietal Bones, 49—Occipital Bone, 50—Occipito-frontalis Muscle, 51—Temporal Bones, 51—Sphenoid or Wedge Bone, 52—Ethmoid Bone, 53—Turbinated Bones, 53—Ossification of Sutures, 53—Bones of the Face, 53—Superior Maxillary Bones, 54—Antrum of Highmore, 54—Malar or Cheek Bones, 54—Lachrymal Bones, 54—Palate Bones, 54—Nasal Bones, 55—Vomer, 55—Inferior Turbinated Bones, 55—Inferior Maxillary Bone or Lower Jaw, 55—Sublingual Gland, 56—Submaxillary Gland, 56.

CHAPTER IV.
The Special Senses 57

The Nose, 57—The Sense of Smell, 58—The Mouth, 59—The Hyoid Bone, 60—The Teeth, 60—The Sense of Taste, 61—Salivary Glands, 61—The Tonsils, 62—The Ear, 63—Eustachian Tubes, 63—Sensation of Hearing, 65—The Eye, 66—Lachrymal Gland, 68—Coats of the Eye, 68—Light Rays and Sight, 70—Accommodation, 72—Color Perception, 73.

The Nose, 57—The Sense of Smell, 58—The Mouth, 59—The Hyoid Bone, 60—The Teeth, 60—The Sense of Taste, 61—Salivary Glands, 61—The Tonsils, 62—The Ear, 63—Eustachian Tubes, 63—Sensation of Hearing, 65—The Eye, 66—Lachrymal Gland, 68—Coats of the Eye, 68—Light Rays and Sight, 70—Accommodation, 72—Color Perception, 73.

CHAPTER V. [Pg 8]
The Nervous System 75

The Cerebrum, 75—The Cerebellum, 78—Pons Variolii, 78—Medulla Oblongata, 78—Spinal Cord, 79—Brain-centers, 81—Motor Tract, 82—Sensory Tract, 82—Reflex Action, 83—Cranial Nerves, 83—Spinal Nerves, 84—Brachial Plexus, 85—Sacral Plexus, 85—The Sympathetic System, 87—The Sympathetic Nerves, 87.

The Cerebrum, 75—The Cerebellum, 78—Pons Variolii, 78—Medulla Oblongata, 78—Spinal Cord, 79—Brain Centers, 81—Motor Pathway, 82—Sensory Pathway, 82—Reflex Action, 83—Cranial Nerves, 83—Spinal Nerves, 84—Brachial Plexus, 85—Sacral Plexus, 85—The Sympathetic System, 87—The Sympathetic Nerves, 87.

CHAPTER VI.
The Rear 88

The Spine, 88—The Vertebræ, 88—Muscles of the Neck, 92—Muscles of the Back, 93.

The Spine, 88—The Vertebrae, 88—Neck Muscles, 92—Back Muscles, 93.

CHAPTER VII.
The Chest 96

The Sternum, 97—The Ribs, 97—Costal Cartilages, 98—Muscles of the Chest, 98—Diaphragm, 98—Mammary Glands, 100.

The Sternum, 97—The Ribs, 97—Costal Cartilages, 98—Muscles of the Chest, 98—Diaphragm, 98—Mammary Glands, 100.

CHAPTER VIII.
The Heart and Blood Flow 101

The Heart, 101—The Pericardium, 101—Cavities of the Heart, 103—The Endocardium, 103—The Valves of the Heart, 103—Circulation, 105—Circulation in the Fetus, 106—Arteries, 107—Veins, 109—Portal Circulation, 109—Pulmonary Circulation, 110—Nerves of the Heart, 110—Heart Sounds, 111—The Heart Beat, 111—Factors Affecting Circulation, 112—The Pulse, 113—Blood Pressure, 114—Nerve Supply of the Blood-vessels, 115—The Blood, 116—Composition of the Blood, 116—Coagulability of the Blood, 117—Blood-corpuscles, 118.

The Heart, 101—The Pericardium, 101—Cavities of the Heart, 103—The Endocardium, 103—The Valves of the Heart, 103—Circulation, 105—Circulation in the Fetus, 106—Arteries, 107—Veins, 109—Portal Circulation, 109—Pulmonary Circulation, 110—Nerves of the Heart, 110—Heart Sounds, 111—The Heart Beat, 111—Factors Affecting Circulation, 112—The Pulse, 113—Blood Pressure, 114—Nerve Supply of the Blood-vessels, 115—The Blood, 116—Composition of the Blood, 116—Coagulability of the Blood, 117—Blood-corpuscles, 118.

CHAPTER IX.
The Lungs and Breathing 121

The Larynx, 121—The Trachea, 123—The Thyroid Gland, 124—The Thymus Gland, 124—The Bronchi, 125—The Lungs, 125—The Pleura, 125—The Mediastinum, 126—Respiration, 127—Air, 129—Respiratory Sounds, 129—Changes in Air in Lungs, 129—Effect of Respiration on Blood, 130—Nervous Mechanism of Respiration, 130—Variations in Respiration, 131.

The Larynx, 121—The Trachea, 123—The Thyroid Gland, 124—The Thymus Gland, 124—The Bronchi, 125—The Lungs, 125—The Pleura, 125—The Mediastinum, 126—Respiration, 127—Air, 129—Respiratory Sounds, 129—Changes in Air in Lungs, 129—Effect of Respiration on Blood, 130—Nervous Mechanism of Respiration, 130—Variations in Respiration, 131.

CHAPTER X. [Pg 9]
The Abdomen and the Digestive and Excretory Organs 132

The Abdominal Cavity, 132—Muscles of the Abdomen, 132—The Peritoneum, 134—Abdominal Regions, 134—Salivary Digestion, 136—The Pharynx, 139—The Esophagus, 138—The Stomach, 138—Gastric Digestion, 139—Vomiting, 140—Intestinal Canal, 141—The Small Intestine, 142—Intestinal Digestion, 143—Absorption in Intestine, 144—The Large Intestine, 145—Food and Metabolism, 147—The Liver, 149—The Gall-bladder, 152—The Pancreas, 153—The Spleen, 153—The Suprarenal Capsules, 154—The Kidneys, 155—The Urine, 156—The Ureters, 159—The Bladder and Urethra, 159.

The Abdominal Cavity, 132—Muscles of the Abdomen, 132—The Peritoneum, 134—Abdominal Regions, 134—Salivary Digestion, 136—The Pharynx, 139—The Esophagus, 138—The Stomach, 138—Gastric Digestion, 139—Vomiting, 140—Intestinal Canal, 141—The Small Intestine, 142—Intestinal Digestion, 143—Absorption in Intestine, 144—The Large Intestine, 145—Food and Metabolism, 147—The Liver, 149—The Gall-bladder, 152—The Pancreas, 153—The Spleen, 153—The Suprarenal Capsules, 154—The Kidneys, 155—The Urine, 156—The Ureters, 159—The Bladder and Urethra, 159.

CHAPTER XI.
The Pelvis and the Reproductive Organs 161

The Pelvis, 161—The Male Generative Organs, 164—The Prostate Gland, 164—The Testes, 165—The Penis, 165—The Female Generative Organs, 165—The Ovaries, 165—The Fallopian Tubes, 166—The Uterus, 167—The Vagina, 168—The External Genitalia in the Female, 169—The Vulva, 169—The Mons Veneris, 169—The Labia Majora, 169—The Labia Minora, 170—The Clitoris, 170—The Meatus Urinarius, 170—The Hymen, 170—The Fourchette, 170—The Perineal Body, 170—The Perineum, 170.

The Pelvis, 161—The Male Reproductive Organs, 164—The Prostate Gland, 164—The Testes, 165—The Penis, 165—The Female Reproductive Organs, 165—The Ovaries, 165—The Fallopian Tubes, 166—The Uterus, 167—The Vagina, 168—The External Genitalia in Women, 169—The Vulva, 169—The Mons Pubis, 169—The Labia Majora, 169—The Labia Minora, 170—The Clitoris, 170—The Urinary Opening, 170—The Hymen, 170—The Fourchette, 170—The Perineal Body, 170—The Perineum, 170.

CHAPTER XII.
The Arms 171

The Shoulder Girdle, 171—The Clavicle, 171—The Scapula, 173—Shoulder Muscles, 174—The Humerus, 175—Upper Arm Muscles, 176—The Ulna, 177—The Radius, 178—The Wrist, 180—The Hand, 181—Meta-carpals, 181—Phalanges, 181—Muscles of the Forearm, 182—Muscles of the Hand, 184—Joints of the Upper Extremity, 185—Blood Supply of the Upper Extremity, 185—Nerves of the Upper Extremity, 186.

The Shoulder Girdle, 171—The Clavicle, 171—The Scapula, 173—Shoulder Muscles, 174—The Humerus, 175—Upper Arm Muscles, 176—The Ulna, 177—The Radius, 178—The Wrist, 180—The Hand, 181—Metacarpals, 181—Phalanges, 181—Muscles of the Forearm, 182—Muscles of the Hand, 184—Joints of the Upper Extremity, 185—Blood Supply of the Upper Extremity, 185—Nerves of the Upper Extremity, 186.

CHAPTER XIII.
The Legs 187

The Femur, 187—Thigh Muscles, 189—The Patella, 192—Joints of the Lower Extremity, 192—The Tibia, 194—The Fibula, 194—The Ankle, 195—The Foot, 195—Metatarsals, 195—Phalanges, 195—Muscles of the Leg, 196—The Blood Supply of the Lower Extremity, 198—Nerves of the Lower Extremity, 199.

The Femur, 187—Thigh Muscles, 189—The Patella, 192—Joints of the Lower Limb, 192—The Tibia, 194—The Fibula, 194—The Ankle, 195—The Foot, 195—Metatarsals, 195—Phalanges, 195—Muscles of the Leg, 196—The Blood Supply of the Lower Limb, 198—Nerves of the Lower Limb, 199.

Table of Contents 201

STRUCTURE AND
FUNCTIONS OF THE BODY.

Body Structure and Functions.


CHAPTER I.
COMPOSITION AND OVERALL STRUCTURE
OF THE BODY.

Anatomy is the study of the physical structure and physiology the study of the normal functions of the human body.

Anatomy is the study of the body's physical structure, and physiology is the study of how the body's normal functions work.

Chemical Constitution of the Body.—In the body only twenty elements have been found. These include carbon, oxygen, hydrogen, nitrogen, sulphur, phosphorus, calcium, magnesium, manganese, chlorin, potassium, and fluorin. For the most part they appear in very complex and highly unstable combinations, though oxygen and nitrogen may be said to exist uncombined in the blood, alimentary canal, and lungs. Hydrogen also occurs in simple form in the alimentary canal, but as the result of fermentation, not as an element of the body.

Chemical Constitution of the Body.—In the body, only twenty elements have been identified. These include carbon, oxygen, hydrogen, nitrogen, sulfur, phosphorus, calcium, magnesium, manganese, chlorine, potassium, and fluorine. Mostly, they exist in very complex and unstable combinations, although oxygen and nitrogen can be found uncombined in the blood, digestive system, and lungs. Hydrogen also appears in simple form in the digestive system, but it is produced through fermentation, not as a component of the body.

Of the organic compounds some contain nitrogen and some do not. The most important of the former are the proteins, which are found only in living bodies and consist of carbon, hydrogen, oxygen, nitrogen, and sulphur combined in very similar proportions. The important proteins in the body are the serum albumen and fibrin found in the blood, myosin in muscle, globulin in the red blood-corpuscles, and casein in the milk. Similar to the proteins but capable of passing through membranes are the [Pg 12] peptones, the final result of protein digestion, from which the albuminoids differ in that they contain no sulphur. Ferments containing nitrogen exist in all the cells of the body, though more particularly in those of the digestive organs, and the coloring matters, as the bilirubin of the bile, are nitrogenous.

Of the organic compounds, some contain nitrogen while others don't. The most important nitrogen-containing compounds are proteins, which are only found in living organisms and are made up of carbon, hydrogen, oxygen, nitrogen, and sulfur in very similar proportions. The key proteins in the body include serum albumin and fibrin found in the blood, myosin in muscle, globulin in red blood cells, and casein in milk. Similar to proteins but capable of passing through membranes are the [Pg 12] peptones, which are the end products of protein digestion, differing from albuminoids in that they don't contain sulfur. Ferments that contain nitrogen are present in all body cells, especially in the digestive organs, and the coloring substances, like bilirubin in bile, are also nitrogenous.

The organic substances that do not contain nitrogen are the carbohydrates or starches, the hydrocarbons or fats, and the acids, of which the most important is carbon dioxide, given off by the lungs.

The organic substances that don't contain nitrogen are carbohydrates or starches, hydrocarbons or fats, and acids, with the most important being carbon dioxide, which is released by the lungs.

The inorganic substances are water, which forms a large percentage of all the tissues and from one-fourth to one-third of the whole body weight, sodium chloride or common salt, which plays an important part in keeping substances in solution, potassium and magnesium chloride, and hydrochloric acid, found in the stomach.

The inorganic substances include water, which makes up a large percentage of all tissues and accounts for about one-fourth to one-third of total body weight, sodium chloride or table salt, which plays a key role in keeping substances dissolved, potassium and magnesium chloride, and hydrochloric acid, which is found in the stomach.

The Cell.—Although the body is a very complex organism, the cell is its unit or foundation. In fact, the body begins life as a single protoplasmic cell, the ovum, which is frequently compared to the amœba, a microscopic animal consisting of a single cell of protoplasm or living substance—a substance not well understood as yet—but possessing practically all the functions of the human body. For, although it has no organs and is homogeneous in structure, the amœba can move by throwing out a process, and can surround and absorb food, which it builds up into new tissue, discarding the waste. The ovum, however, differs from the amœba in that it has a transparent limiting membrane and contains a darker spot, the nucleus. This in turn contains another smaller spot, the nucleolus, while through the protoplasm, which is semi-fluid, extends a fine network that seems to hold it in place.

The Cell.—Even though the body is a very complex organism, the cell is its basic unit or foundation. In fact, the body starts as a single protoplasmic cell called the ovum, which is often compared to the amœba, a microscopic creature made up of just one cell of protoplasm or living substance—a substance that we still don't fully understand—but that has nearly all the functions of the human body. While it lacks organs and is uniform in structure, the amœba can move by extending a process and can surround and absorb food, which it then converts into new tissue, getting rid of waste in the process. The ovum, however, is different from the amœba because it has a clear membrane around it and contains a darker area called the nucleus. Inside the nucleus is another smaller area, the nucleolus, while through the semi-fluid protoplasm runs a delicate network that seems to hold it together.

The ovum is very small, about ¹/₁₂₅ inch in diameter, and after fertilization grows by segmentation, the nucleus dividing in two and the protoplasm grouping itself anew about the two nuclei. This division continues, each cell dividing and forming two, or sometimes four, new [Pg 13] cells, all of which at first appear alike. By degrees, however, differentiation takes place and different groups of cells assume different characteristics. Thus the various tissues are gradually developed, each with a structure and a function of its own, and are distributed among the various organs, each organ consisting of several tissues. During the process of growth and even after full growth of the body is attained old cells are continually dying and being replaced by new ones.

The ovum is very small, about ¹/₁₂₅ inch in diameter, and after fertilization, it grows by dividing. The nucleus splits into two, and the protoplasm reorganizes around the two nuclei. This division keeps happening, with each cell splitting and forming two, or sometimes four, new [Pg 13] cells, all of which initially look alike. Gradually, however, differentiation occurs, and different groups of cells develop distinct characteristics. This leads to the gradual formation of various tissues, each with its own structure and function, which are spread across different organs, with each organ made up of several tissues. Throughout the growth process and even after the body has fully grown, old cells continuously die and are replaced by new ones.

The typical cell is circular, but through being squeezed together in the tissues or for some other reason the cells vary in shape in different parts, being at times hexagonal, spindle-shaped, or columnar. Yet, whatever their differences in shape or other characteristics, they all live the same sort of life. All protoplasm absorbs oxygen when it comes in contact with it and in the process of combining with it is in part burned or oxidized, with the consequent setting free of heat and other forms of energy and the formation of carbon dioxide. So long as the body is alive, therefore, whether it is in a state of activity or of rest, it is the seat of constant chemical change throughout all its cells, and to these chemical changes are due all the forms of energy manifested by the body. For energy is never destroyed, though it may appear in a different form, and the elements of the human body are so combined that their energy may be liberated and manifested in the different functions the body exhibits.

The typical cell is round, but when they get squished together in tissues or for some other reason, the cells change shape in different areas, sometimes becoming hexagonal, spindle-shaped, or column-like. However, despite their shape or other differences, they all function in a similar way. All protoplasm takes in oxygen when it comes into contact with it, and in the process of combining with it, it gets partially burned or oxidized, which releases heat and other forms of energy and creates carbon dioxide. As long as the body is alive, whether active or at rest, it undergoes constant chemical changes in all its cells, and these chemical changes are responsible for all the energy forms the body displays. Energy is never destroyed, even though it can change into different forms, and the elements of the human body are arranged in a way that allows their energy to be released and used in the various functions the body performs.

The fundamental tissues of the body are the epithelial tissues, the connective tissues, including the cartilaginous and bony tissues, and the muscular and nervous tissues. Of these the epithelial tissues serve as a protection to the surface of other tissues; the connective tissues together form a framework for the support and general protection of the other tissues; while energy is expended by muscular and nervous tissue, the latter directing the former in its movements. All the tissues are inter-dependent and the organs work together. Besides cells every tissue contains a certain amount of lifeless matter, [Pg 14] the intercellular substance, which was at some time produced by the cells.

The fundamental tissues of the body are the epithelial tissues, the connective tissues, which include cartilage and bone, as well as muscular and nervous tissues. The epithelial tissues act as a protective layer for other tissues; the connective tissues create a framework that supports and protects the other tissues; while muscular and nervous tissues use energy, with the nervous tissue guiding the muscular tissue in its actions. All the tissues rely on each other, and the organs function collectively. In addition to cells, each tissue contains a certain amount of non-living matter, [Pg 14] the intercellular substance, which was produced by the cells at some point.

Fig. 1.—Epithelium: 1, pavement epithelium; 2, columnar epithelium; 3, ciliated epithelium; 4, stratified epithelium.

Fig. 1.—Epithelium: 1, flat epithelial cells; 2, columnar epithelial cells; 3, ciliated epithelial cells; 4, layered epithelial cells.

In epithelial tissue there is little intercellular substance, the cells being close together and arranged generally as a skin or membrane covering external or internal surfaces. When there are several layers of cells, the deepest are columnar in shape and the others become more and more flattened and scale-like as they approach the surface, where they are gradually rubbed off and replaced by the growth of new cells from below. This stratified epithelium, as it is called, is found wherever a surface is exposed to friction, as in the skin and in the mucous membrane of the mouth, pharynx, and esophagus, and in that of the vagina and the neck of the uterus. In simple epithelium, where there is only a single layer of cells, the cells may be pavement or hexagonal, columnar, glandular, or ciliated, according to their different functions. The flat pavement cells occur where a very smooth surface is required, as in the heart, lungs, blood-vessels, serous cavities, etc. None of these surfaces communicate directly with the external surface of the body and the name endothelium is substituted for epithelium. The columnar form of cell in the intestine facilitates the passage of leucocytes between the cells. In glandular epithelium the cells vary according to the gland in which they occur, their [Pg 15] protoplasm being filled with the material the gland secretes. Finally, ciliated epithelium is composed of columnar cells with cilia or little hair-like processes upon their free surface which serve to send secreted fluids and other matters along the surfaces where they occur, as in the air passages, parts of the generative organs, the ventricles of the brain, and the central canal of the spinal cord.

In epithelial tissue, there's very little space between cells; they are packed closely together, usually forming a layer that covers external or internal surfaces. When there are multiple layers of cells, the ones at the bottom are shaped like columns, while the cells closer to the surface become increasingly flat and scale-like. These surface cells eventually wear away and are replaced by new cells growing from below. This stratified epithelium, known as a protective layer, can be found wherever surfaces are exposed to friction, like the skin, as well as in the mucous membranes of the mouth, throat, esophagus, vagina, and cervix. In simple epithelium, which has just one layer of cells, the cells can be flat or hexagonal, columnar, glandular, or ciliated, depending on their specific functions. Flat pavement cells cells are found where a smooth surface is important, such as in the heart, lungs, blood vessels, and serous cavities. These surfaces do not connect directly to the external body, so the term endothelium is used instead of epithelium. The columnar cells in the intestine help with the movement of white blood cells between them. In glandular epithelium, the cells differ based on the gland they belong to, with their cytoplasm filled with the substances that the gland produces. Finally, ciliated epithelium consists of columnar cells that have tiny hair-like structures called cilia on their surface, which help move secreted fluids and other materials along the surfaces where they are found, such as in the airways, parts of the reproductive system, the brain’s ventricles, and the spinal canal.

Connective tissue has a great deal of intercellular substance. One form, areolar tissue, is composed of a loose network of fine white fibers with a few yellow elastic fibers interspersed and with cells lying in the spaces between the fibers. It connects and surrounds the different organs and parts, holding them together, yet allowing free motion, and is one of the most extensively distributed of the tissues. It is continuous throughout.

Connective tissue has a lot of intercellular substance. One type, areolar tissue, consists of a loose network of fine white fibers with some yellow elastic fibers mixed in, and with cells positioned in the gaps between the fibers. It connects and surrounds various organs and parts, holding them together while still allowing for free movement, and it's one of the most widely distributed tissues in the body. It is continuous throughout.

Fig. 2.—Section of bladder epithelium. (Hill.)

Fig. 2.—Section of bladder epithelium. (Hill.)

Closely allied to the areolar is the fibrous tissue, in which the white fibers lie close together and run for the most part in one direction only. This is found in ligaments, joints and tendons, as also in such fibrous protective membranes as the periosteum, dura mater, the fasciæ of muscles, etc. Fibrous tissue is silvery white in appearance and is very strong and tough, yet pliant. It is not extensile.

Closely related to the areolar tissue is the fibrous tissue, where the white fibers are close together and mostly run in a single direction. This type of tissue is found in ligaments, joints, tendons, and in fibrous protective membranes like the periosteum, dura mater, and the fascia of muscles, among others. Fibrous tissue has a silvery white appearance and is very strong and tough, yet flexible. It does not stretch.

Elastic tissue, on the other hand, has a large predominance of yellow elastic fibers and is very extensile and elastic, though not so strong as the fibrous. It is found in the walls of the blood-vessels, [Pg 16] especially the arteries, in the walls of the air tubes, in the ligaments of the spine, etc.

Elastic tissue, however, contains a lot of yellow elastic fibers and is highly stretchy and elastic, though it's not as strong as fibrous tissue. It's located in the walls of blood vessels, [Pg 16] particularly in arteries, in the walls of airways, in the ligaments of the spine, and so on.

Fatty or adipose tissue is formed by the deposit of fat in the cells of the areolar tissue and is found in most parts where the areolar tissue occurs, though it varies largely in amount in different parts. It is found pretty generally under the skin, fills in inequalities about various organs and about the joints, and exists in large quantities in the marrow of the long bones. In moderate amounts it gives grace to the form and constitutes an important reserve fund.

Fatty or adipose tissue is created by the buildup of fat in the cells of areolar tissue and is present in most areas where this type of tissue is found, although its quantity varies significantly in different regions. It is commonly located beneath the skin, helps to smooth out irregularities around various organs and joints, and is found in large amounts within the marrow of long bones. In moderate amounts, it adds shape to the body and serves as an important reserve of energy.

Fig. 3.—Adipose tissue (Leroy): a, Fibrous tissue; b, fat cells; c, nucleus of fat cells; d, fatty acid crystals in fat cells.

Fig. 3.—Fat tissue (Leroy): a, Connective tissue; b, fat cells; c, nucleus of fat cells; d, fatty acid crystals in fat cells.

Cartilage consists of groups of nucleated cells in intercellular substance. It is very firm, yet highly elastic, and serves in the joints to break the force of concussion of the harder and less elastic bones. Except when it occurs at the end of a bone, it is covered with a membrane called the perichondrium, which carries its blood supply. In the nose, ear, larynx and trachea it serves to give shape, to keep the [Pg 17] passages open, and to afford attachment for muscles. Most of the skeleton of the fetus consists of cartilage, which later develops into bone.

Cartilage is made up of groups of nucleated cells suspended in a substance that fills the spaces between them. It's very strong but also quite flexible, helping to absorb shock in the joints to protect the harder and less flexible bones. Except at the ends of bones, cartilage is covered by a membrane called the perichondrium, which provides its blood supply. In the nose, ears, larynx, and trachea, it helps maintain shape, keeps the [Pg 17] passages open, and provides a point for muscles to attach. Most of the skeleton of a fetus is made of cartilage, which later transforms into bone.

Bone.—In bone the intercellular tissue is rendered hard by the deposit of mineral salts, the resulting material being of great strength and rigidity. The texture may be close and dense like ivory or open and spongy, the difference lying merely in the fact that the one has fewer spaces between the solid particles than the other. There is usually a hard, compact layer on the exterior of the bone, as that is where the greatest cross-strain comes, especially in the long bones, while within is the cancellous or spongy tissue, which gives lightness to the bone and is capable of withstanding enormous pressure, though it can bear little cross-strain.

Bone.—In bone, the tissue between cells becomes hard due to the buildup of mineral salts, resulting in a material that is very strong and rigid. The texture can be either smooth and dense like ivory or porous and spongy; the difference is simply that one has fewer gaps between the solid particles than the other. There is usually a hard, compact layer on the outer surface of the bone, as this area experiences the most cross-strain, especially in long bones. Inside, there is cancellous or spongy tissue, which makes the bone lighter and can handle a lot of pressure, though it struggles with cross-strain.

Fig. 4.—Cross-section of compact bone tissue. (After Sharpey.)

Fig. 4.—Cross-section of compact bone tissue. (After Sharpey.)

Structure of Bone.—The hard substance in bone is always arranged in lamellæ or bundles of bony fibers, which in cancellous tissue meet to form a kind of lattice-work, while in the dense tissue they are generally arranged in rings about the Haversian canals, channels through which the blood-vessels pass through the bone longitudinally. Between the lamellæ are spaces called lacunæ, in which lie branched cells, the spaces being connected with each other and with the Haversian canals by numerous tiny canals or canaliculi, [Pg 18] by which nutrient material finds its way from the Haversian canals to all parts of the bone.

Structure of Bone.—The hard material in bone is always arranged in layers or bundles of bone fibers, which in spongy tissue come together to create a sort of lattice-work, while in the compact tissue they are usually organized in rings around the Haversian canals, channels that allow blood vessels to travel through the bone lengthwise. Between the layers are spaces called lacunæ, where branched cells reside, and these spaces are interconnected with each other and with the Haversian canals through numerous tiny channels or canaliculi, [Pg 18] allowing nutrients to move from the Haversian canals to all areas of the bone.

Within the bone is the medulla or marrow, which is of two varieties: the yellow, which is largely fat and is found in the long bones of adults, and the red, which is nearly three-fourths water and is found in most of the other adult bones and in the bones of the fetus and of the infant.

Within the bone is the medulla or marrow, which comes in two types: yellow, which is mostly fat and found in the long bones of adults, and red, which is almost three-fourths water and is found in most other adult bones as well as in the bones of the fetus and the infant.

Lining the medullary and cancellous cavities is a delicate connective tissue lining, the endosteum, which contains many bone-forming cells, while on the outside of the bone, except at the articular ends, is the periosteum with its outer protective layer and its inner vascular layer containing osteoblasts or bone-forming cells. The periosteum is essential for the growth of new bone where the old bone has died, and if the periosteum is removed from healthy bone the part beneath is liable to die, as it is by the constant growth of the osteoblasts that the bone grows and is renewed. In the repair of broken bones tissue is formed between and around the broken ends.

Lining the inner and outer cavities of the bone is a thin layer of connective tissue called the endosteum, which contains many bone-forming cells. On the outside of the bone, except at the joint surfaces, is the periosteum, which has an outer protective layer and an inner vascular layer filled with osteoblasts or bone-forming cells. The periosteum is crucial for the growth of new bone when old bone has died. If the periosteum is removed from healthy bone, the underlying area is likely to die, because it's the continuous activity of the osteoblasts that allows the bone to grow and regenerate. When bones break, tissue forms between and around the broken ends.

Bone Formation.—Most of the skull and face bones begin as membranes of connective tissue, that is, are formed in membrane. Bones are also formed in cartilage, the bone formation in this case beginning from centers of ossification, where the deposit of lime salts in the intercellular substance begins, the salts coming to the centers dissolved in the plasma. Such a center of growth in a bone is called the epiphysis and is separated from the main part of the bone or diaphysis by cartilage until full growth is attained, when ossification becomes complete. So in surgery, in working on the bones of children, part of the epiphysis should always be left for the sake of future growth. The outer shell of compact tissue is deposited by the periosteum.

Bone Formation.—Most bones in the skull and face start as layers of connective tissue, meaning they develop from membranes. Bones can also form in cartilage, with the process beginning at centers of ossification, where lime salts start to deposit in the spaces between cells, coming to those centers dissolved in the plasma. This area of growth in a bone is called the epiphysis and is separated from the main part of the bone, known as the diaphysis, by cartilage until full growth is reached, at which point ossification is complete. Therefore, in surgery involving children's bones, it's important to leave part of the epiphysis intact for future growth. The outer layer of compact tissue is formed by the periosteum.

Chemical Composition of Bone.—Chemically bone is composed of about one-third organic or animal matter, largely gelatine, and [Pg 19] two-thirds inorganic matter, including various salts of calcium, magnesium, and sodium. In young children the animal matter predominates and the bones are soft and often bend instead of breaking, only the outside shell on one side giving way, as in “green-stick” fracture. In rickets there is a deficiency of lime salts, but the increased brittleness of the bones in old age is due, not to increase of mineral matter, but to the less spongy texture of old bones.

Chemical Composition of Bone.—Bone is made up of about one-third organic or animal material, mainly gelatin, and [Pg 19] two-thirds inorganic material, which includes different salts of calcium, magnesium, and sodium. In young children, the animal material is more dominant, making the bones soft and able to bend instead of breaking; only the outer layer on one side gives way, similar to a “green-stick” fracture. In rickets, there is not enough lime salts, but the increased brittleness of bones in old age isn't because there’s more mineral content, but rather due to the less spongy structure of older bones.

Classification and Function of Bones.—There are in the body some two hundred bones, which may be classified as long, short, flat, and irregular. Occasionally an irregular bone develops in a fontanelle, the membranous opening at the juncture of the sutures of the skull. This is known as a Wormian bone. It is not, however, included in the two hundred, as are not the sesamoid bones or bones developed in tendons, with the exception of the patella or knee-cap.

Classification and Function of Bones.—The body has about two hundred bones, which can be categorized as long, short, flat, and irregular. Sometimes, an irregular bone forms in a fontanelle, the soft spot where the skull sutures meet. This is referred to as a Wormian bone. However, it isn't counted in the two hundred, nor are the sesamoid bones or those that develop in tendons, except for the patella or kneecap.

Long bones are developed in cartilage and consist of a shaft, two extremities, and various processes. They are more or less curved to give them strength and grace. They serve as supports and act as levers for purposes of motion and the exercise of power. Since a hollow cylinder is just as strong as a solid one of the same size, the weight coming only on the outer shell, the great bones which are accountable for weight and which need to be light themselves have hollow shafts, composed chiefly of compact tissue with a central medullary canal. The ends, however, are expanded in order to make better connection at the joints and to afford broad surfaces for muscular attachment, cancellous tissue being used in them for lightness and strength. The large spongy ends also give elasticity and lessen jar, and by bringing the tendons to the bone at a greater angle increase their effectiveness. Blood is brought to the long bones not only by the vessels of the periosteum but by the medullary artery, which penetrates the compact tissue by the nutrient foramen and divides into an ascending and a descending branch. [Pg 20]

Long bones develop from cartilage and have a shaft, two ends, and various projections. They are curved to provide strength and elegance. They act as supports and levers for movement and exerting force. Since a hollow cylinder is as strong as a solid one of the same size, with weight distributed only on the outer shell, the large bones that bear weight and need to be light have hollow shafts made mainly of dense tissue with a central medullary canal. The ends are broader to create better connections at the joints and provide wider surfaces for muscle attachment, using spongy tissue for reduced weight and increased strength. The large, spongy ends also add flexibility and reduce shock, while positioning the tendons at a wider angle improves their effectiveness. Blood reaches the long bones through the vessels of the periosteum and the medullary artery, which enters the dense tissue through the nutrient foramen and splits into an ascending and descending branch. [Pg 20]

Short bones are spongy throughout. They are used for strength and where little motion is required.

Short bones are spongy all the way through. They're used for strength and in areas where minimal movement is needed.

Flat bones are composed of two thin layers of compact tissue with a varying amount of cancellous tissue between, and are for protection and muscular attachment. The cancellous material between the two layers or tablets of the skull is called the diploë.

Flat bones consist of two thin layers of dense tissue with a varying amount of spongy tissue in between. They serve to protect and provide attachment for muscles. The spongy material found between the two layers or tables of the skull is referred to as the diploë.

Eminences and depressions occur on bones and when they are not articular are for the attachment of ligaments and muscles. If they are articular, they help to form joints.

Eminences and depressions appear on bones, and when they aren’t articular, they serve as attachment points for ligaments and muscles. If they are articular, they contribute to the formation of joints.

As a whole the bony framework serves to keep the soft parts in place, to support and protect them, and to aid in locomotion. The bones of the head and trunk support and protect organs; those of the arms are for tact and prehension; those of the lower extremities are for support and locomotion.

As a whole, the skeletal structure helps keep the soft tissues in place, supports and protects them, and assists with movement. The bones in the head and torso support and shield organs; the bones in the arms are used for touch and grasping; the bones in the legs support the body and help with movement.

Normally bones have little sensibility, but when inflamed they are extremely sensitive and painful.

Normally, bones have very little feeling, but when they are inflamed, they become highly sensitive and painful.

Joints.—The bones are connected with and move upon one another by means of joints. These joints are of three kinds: 1. Immovable, where the adjacent margins of the bones are closely applied, with little fibrous tissue between, as in the sutures of the head; 2. those with limited motion, which are very strong, the parts being connected with tough fibro-cartilage; and 3. freely movable. In this last group the articulating surfaces are covered with cartilage, which again is lined with a delicate synovial membrane which secretes a small amount of lubricating fluid, the synovial fluid, to reduce friction. Their surfaces are also sometimes deepened by the presence of inter-articular fibro-cartilages. Bursæ or sacs of synovial membrane occur outside the joints under tendons and ligaments to reduce friction.

Joints.—The bones are connected and move against each other through joints. There are three types of joints: 1. Immovable joints, where the edges of the bones fit closely together with little fibrous tissue in between, like in the sutures of the skull; 2. joints with limited movement, which are quite strong, connected by tough fibro-cartilage; and 3. freely movable joints. In this last group, the surfaces that meet are covered with cartilage, which is lined by a thin synovial membrane that secretes a small amount of lubricating fluid called synovial fluid to reduce friction. Sometimes, the surfaces are also deepened by the presence of inter-articular fibro-cartilages. Bursae or sacs made of synovial membrane can be found outside the joints, beneath tendons and ligaments, to help reduce friction.

The nature and extent of the motion of a joint is defined and the bones are held together by strong bands of fibrous tissue or ligaments, these ligaments being more fully developed in joints where there is great [Pg 21] freedom of motion or where there is great weight to be supported. In a ball-and-socket joint, such as the hip, there is a ligament in the form of a strong capsule which surrounds the joint on all sides and limits its motion, while hinge joints, like the elbow, and pivot joints, such as that formed by the atlas on the axis, have lateral ligaments that allow of freer motion. In the shoulder-joint, which is the most freely movable joint in the body, the capsular ligament is very lax.

The type and range of movement in a joint are defined, and the bones are connected by strong bands of fibrous tissue called ligaments. These ligaments are more developed in joints that allow for a lot of movement or need to support significant weight. In a ball-and-socket joint, like the hip, there’s a strong capsule-like ligament that surrounds the joint and restricts its movement. In contrast, hinge joints, like the elbow, and pivot joints, such as the one between the atlas and axis, have lateral ligaments that permit more freedom of motion. The shoulder joint, which is the most movable joint in the body, has a very loose capsular ligament.

In general the kinds of motion possible in joints may be said to be flexion, extension, abduction, adduction, circumduction, and rotation.

In general, the types of movement possible in joints can be described as flexion, extension, abduction, adduction, circumduction, and rotation.

When much violence is applied to a joint and no dislocation results, as in a sprain, there is often much stretching and even laceration of the ligaments.

When a lot of force is applied to a joint and no dislocation occurs, like in a sprain, there can often be significant stretching and even tearing of the ligaments.

Muscle.—The flesh, which forms a large proportion of the weight of the body, consists of muscular tissue. Of this two kinds are found: 1. The striated or striped muscle of animal life, which is under the control of the will and so is known as voluntary muscle, and 2. the unstriped or smooth muscle of organic life over which we have no control, that is, the involuntary muscle. Each fiber of striped muscle has an elastic, membranous sheath, the sarcolemma, and consists of rod-shaped cells with a nucleus along the edge, set end to end and having crosswise striations. In unstriated muscle the fibers, which have no sarcolemma, consist of oval or spindle-shaped cells, with a nucleus much smaller than that of striped muscle and situated in the middle. In both kinds of muscle the fibers are bound together with connective tissue and blood-vessels into fasciculi or bundles, and many bundles go to make up a muscle. The muscle in turn has a connective tissue envelope or sheath, the fascia. These fasciæ are found throughout the body, the superficial ones being just beneath the skin, while the deep ones not only form sheaths for the various muscles but form partitions between them and serve to strengthen their attachments. [Pg 22] The striped muscles are those of motion, while the unstriped occur in the hollow organs, surrounding the cavity and in some cases lessening its capacity by their contraction.

Muscle.—The flesh, which makes up a large part of the body's weight, consists of muscle tissue. There are two types: 1. Striated or striped muscle, which is under voluntary control and is known as voluntary muscle, and 2. Unstriped or smooth muscle, which we can't control, known as involuntary muscle. Each fiber of striped muscle has an elastic, membranous covering called the sarcolemma, and is made up of rod-shaped cells with a nucleus at the edge, arranged end to end and having crosswise striations. In unstriated muscle, the fibers lack sarcolemma and consist of oval or spindle-shaped cells, with a much smaller nucleus located in the center. In both types of muscle, fibers are held together by connective tissue and blood vessels into bundles or fasciculi, and many bundles combine to form a muscle. Each muscle is covered by a connective tissue sheath known as fascia. These fascias are present throughout the body, with the superficial ones lying just beneath the skin, while the deeper ones not only encase various muscles but also create partitions between them and help strengthen their connections. [Pg 22] The striped muscles are responsible for movement, while the unstriped muscles are found in hollow organs, surrounding their cavities and, in some cases, reducing their capacity by contracting.

An intermediate form of muscle known as cardiac muscle occurs in the heart. Here the fibers have striations but the nucleus is generally in the middle of the cell and the fibers branch and run together.

An intermediate type of muscle called cardiac muscle is found in the heart. In this muscle, the fibers have striations, but the nucleus is usually located in the center of the cell, and the fibers branch out and connect with each other.

Fig. 5.—Voluntary muscle (Leroy). A, Three voluntary fibers in long sections: a, three voluntary muscle fibers; b, nuclei of same; c, fibrous tissue between the fibers (endomysium); d, fibers separated into sarcostyles. B, Fiber (diagrammatic): a, dark band; b, light band; c, median line of Hensen; d, membrane of Krause; e, sarcolemma; f, nucleus. C: a, Light band; b, dark band; c, contracting elements; d, row of dots composing the membrane of Krause; e, slight narrowing of contracting element aiding in production of median line of Hensen.

Fig. 5.—Voluntary muscle (Leroy). A, Three voluntary fibers in long sections: a, three voluntary muscle fibers; b, nuclei of same; c, fibrous tissue between the fibers (endomysium); d, fibers separated into sarcostyles. B, Fiber (diagrammatic): a, dark band; b, light band; c, median line of Hensen; d, membrane of Krause; e, sarcolemma; f, nucleus. C: a, Light band; b, dark band; c, contracting elements; d, row of dots making up the membrane of Krause; e, slight narrowing of contracting element helping in the production of median line of Hensen.

In life muscle appears more or less translucent and is contractile and alkaline, but in death it loses its translucency and becomes rigid, at the same time giving off in decomposition much carbon dioxide, so that its reaction is acid. This phenomenon of the muscles becoming rigid in death is called rigor mortis and occurs generally a few hours after [Pg 23] death, though it may come at once or be considerably delayed. It may last anywhere from a few moments to several days but generally lasts from twenty-four to thirty-six hours. It is probably due to the formation in the muscle of myosin, a substance which probably comes from myosinogen in the living muscle and which is closely akin to the fibrin of blood. Probably the myosin or what precedes it causes clotting of the muscle just as fibrin or what precedes it causes clotting of the blood.

In life, muscle appears somewhat see-through and is stretchy and basic, but after death, it loses its transparency and becomes stiff. During decomposition, it releases a lot of carbon dioxide, making its reaction acidic. This process where muscles stiffen after death is called rigor mortis and usually happens a few hours after [Pg 23] death, although it can occur right away or be significantly delayed. It can last from just a few moments to several days, but it typically lasts between twenty-four to thirty-six hours. This is likely due to the formation of myosin in the muscle, a substance that probably comes from myosinogen in living muscle and is closely related to blood fibrin. It seems that myosin, or a precursor to it, causes the muscle to clump together just like fibrin, or what comes before it, causes the blood to clump.

Fig. 6.—Three voluntary muscle fibers from an injected muscle, showing network of blood capillaries. (Hill.)

Fig. 6.—Three voluntary muscle fibers from an injected muscle, showing a network of blood capillaries. (Hill.)

The muscles vary in shape in different parts of the body, being long and slender in the limbs and broad and flat in the trunk. They are attached chiefly to bones but also to cartilages, ligaments, and skin, either by means of tendons, which are cords or bands of white inelastic fibrous tissue, or by means of aponeuroses, membranous expansions of the same nature. Most voluntary muscles consist of a belly and two ends or tendons. The origin is the fixed point from which it acts while the movable point upon which it acts is known as its insertion.

The muscles come in different shapes throughout the body, being long and slim in the limbs and broad and flat in the torso. They mainly attach to bones but also connect to cartilages, ligaments, and skin through tendons, which are cords or bands of tough, inelastic tissue, or through aponeuroses, which are flat, membranous expansions made of the same material. Most voluntary muscles have a central part called a belly and two ends or tendons. The origin is the fixed point where it starts to act, while the movable point where it applies force is called the insertion.

Action of the Muscles.—When attached to bones, muscles are distributed in three ways: 1. When it is necessary to produce much motion rapidly, a short muscle is used. 2. When a part needs to be moved far and much contraction on the part of the muscle is, therefore, needed, the muscle is very long, as in the case of the sartorius [Pg 24] muscle, which shortens half its length. 3. Finally, where less distance has to be covered but greater power is required, tendons are used, as in this case the contraction is powerful but does not carry the part far.

Action of the Muscles.—When connected to bones, muscles are arranged in three ways: 1. For quick and significant movement, a short muscle is utilized. 2. When a part needs to move a long distance and requires significant contraction of the muscle, the muscle is very long, like the sartorius [Pg 24] muscle, which shortens by half its length. 3. Lastly, where the distance moved is shorter but more strength is needed, tendons are applied, as in this situation, the contraction is strong but does not move the part far.

In performing the mechanical work of the body the muscles are aided by the fact that the bones, to which they are largely attached, are set together loosely and form a set of levers, on which the muscles act to perform certain definite acts. All three classes of levers occur: 1. where the fulcrum is between the weight and the power, as in the case of the head, which is balanced by the muscles of the neck on the vertebræ; 2. where the weight is between the fulcrum and the power, as when a person raises himself upon his toes; and 3. where the power is between the fulcrum and the weight, as when the biceps is used to raise a weight held in the hand. The erect position of the body is difficult to maintain because the center of gravity is high up, and it is by the contraction of many muscles in the legs, thighs, back, abdomen, and neck that the body is balanced upright upon the feet.

In doing the body's mechanical work, the muscles are supported by the fact that the bones, which they are mostly attached to, are loosely connected and create a system of levers that the muscles use to perform specific actions. All three types of levers are present: 1. where the fulcrum is between the weight and the effort, like with the head, which is supported by the neck muscles on the vertebrae; 2. where the weight is between the fulcrum and the effort, as when someone lifts themselves onto their toes; and 3. where the effort is between the fulcrum and the weight, as when the biceps lift a weight held in the hand. Maintaining an upright position is challenging because the center of gravity is high, and it is through the contraction of various muscles in the legs, thighs, back, abdomen, and neck that the body stays balanced on the feet.

Physiology of Muscle.Irritability or sensitiveness to stimulation and contractility or the power to contract are the two most important functions of muscle. Contraction occurs in response to nervous energy brought by the nerves, a nerve filament going to each muscle fiber, into which it plunges, its substance being lost and its sheath becoming continuous with that of the muscle fiber. Any irritant, as heat, electricity, etc., when applied to the nerve, causes the muscle to contract. Moreover, muscle has an irritability of its own and can contract independently of the nervous system. In contracting it shortens and thickens, bringing the two ends closer together, and becomes firm and rigid. The amount of contraction depends upon the strength of the stimulus and the irritability of the muscle. The minimal stimulus is the least stimulus that will cause a contraction [Pg 25] and the maximal is one that will cause the greatest contraction. The work done depends in like manner upon the strength of the stimulus. During contraction certain sounds are given off called muscle sounds, which can be heard with the stethoscope but have no special significance.

Physiology of Muscle.Irritability or sensitivity to stimulation and contractility or the ability to contract are the two main functions of muscle. Contraction happens in response to nervous energy delivered by the nerves, with a nerve filament extending to each muscle fiber, penetrating it, losing its substance, and its sheath becoming continuous with that of the muscle fiber. Any irritant, like heat or electricity, when applied to the nerve, triggers the muscle to contract. Additionally, muscle has its own irritability and can contract independently of the nervous system. When it contracts, it shortens and thickens, pulling the two ends closer together, and becomes firm and rigid. The degree of contraction is based on the strength of the stimulus and the irritability of the muscle. The minimal stimulus is the smallest stimulus that will cause a contraction [Pg 25] and the maximal is the one that will cause the greatest contraction. The amount of work done similarly depends on the strength of the stimulus. During contraction, certain sounds known as muscle sounds are produced, which can be heard with a stethoscope but have no particular significance.

The muscles which have the greatest power of rapid contraction are generally attached to levers. Indeed, striated muscle is characterized by the rapidity and strength with which it works, though its rhythmic motion is slight. Smooth muscle, on the other hand, is characterized by its great force, considerable rhythm, considerable tone, and slight rapidity, that is, its contraction is slower and lasts longer than that of striated muscle. Cardiac muscle is characterized by great rhythm and force, fair rapidity, and slight tonicity, tonicity being the amount of tone or readiness to work. For even in sleep muscle is always in tone, that is, ready to do its work. It is this that makes the difference in appearance between a living and a dead person and enables one to spring to his feet at night if he hears a noise, a thing he could not do if his muscles were wholly relaxed. Thus, rapidity is the great function of striated, tonicity of smooth, and rhythm of cardiac muscle. In paralysis the muscles droop and lose their tone. Muscles are frequently the seat of rheumatic disorders.

The muscles that can contract quickly and powerfully are usually connected to levers. Striated muscle, in particular, is known for its quickness and strength, even though its movement is not very rhythmic. Smooth muscle, on the other hand, is defined by its considerable strength, noticeable rhythm, decent tone, and slower contraction, meaning it contracts more slowly and lasts longer than striated muscle. Cardiac muscle is characterized by its strong rhythm and force, decent rapidity, and slight tonicity, which refers to the level of tone or readiness to work. Even when asleep, muscles are always toned, meaning they are ready to act. This is what makes living beings look different from those who are dead and allows someone to jump up at night if they hear a noise; they wouldn't be able to do this if their muscles were completely relaxed. Therefore, rapidity is the key function of striated muscle, tonicity for smooth muscle, and rhythm for cardiac muscle. In paralysis, muscles become limp and lose their tone. Muscles are often affected by rheumatic disorders.

When set free, potential energy accomplishes work. In muscle there is a good deal of potential energy, which is set free as heat and as work accomplished. Even when the muscles are at rest, chemical changes are going on and heat is being produced, though more heat is produced when they are functioning. If the body depended upon its gross motions for all its heat it would grow cold while a person rested. The respiratory organs, however, and the heart are always working and chemical changes are constantly taking place.

When released, potential energy does work. Muscles contain a lot of potential energy, which is released as heat and as work performed. Even when the muscles are at rest, chemical changes occur, generating heat, although more heat is produced when they are active. If the body relied only on its large movements for heat, it would cool down while a person was resting. However, the respiratory system and the heart are always working, and chemical changes are continuously happening.

Ordinarily a muscle has some object in contracting, such as the raising of a load, and it contracts voluntarily more or less according to the [Pg 26] weight of the load. The amount of work done is calculated in foot-pounds or gram-meters, that is, the energy required to raise one pound one foot or one gram one meter. As a rule the muscles with the longest fibers, as the biceps, do the most work and those with a large number of fibers do more than those with less. It has been calculated that whereas an engine gives back one-twelfth of the energy of the coal consumed, muscle liberates one-fourth of the energy brought to it in the form of food. During activity the glycogen or sugar in the muscle is used up and the muscle becomes more acid, owing to the lactic acid that is formed. The carbon is taken in and carbon dioxide given off. Nitrogen puts the muscle in condition to do its work but is not so much used up in the work as is the carbohydrate material. So it is the non-nitrogenous matter that does the work and any increase in urea, the end-product of protein metabolism, is mere wear and tear.

Typically, a muscle has a specific goal when it contracts, like lifting a load, and it contracts voluntarily to varying degrees based on the weight of that load. The amount of work done is measured in foot-pounds or gram-meters, meaning the energy needed to lift one pound one foot or one gram one meter. Generally, muscles with longer fibers, like the biceps, do the most work, and those with a larger number of fibers perform better than those with fewer. It has been estimated that while an engine returns one-twelfth of the energy from the coal consumed, muscle releases one-fourth of the energy obtained from food. During activity, the glycogen or sugar in the muscle is consumed, leading to an increase in acidity due to lactic acid production. Carbon is absorbed while carbon dioxide is expelled. Nitrogen helps prepare the muscle for work, but it isn’t used up as much during the activity compared to carbohydrates. Therefore, it's the non-nitrogenous substances that provide the energy for work, and any rise in urea, the end-product of protein metabolism, is simply a result of normal wear and tear.

Sudden heat or cold causes muscular contraction and moderate heat favors both muscular and nervous irritability. Moderate cold, however, lessens the force of contraction and below zero muscle very largely loses its irritability without necessarily becoming rigid.

Sudden heat or cold leads to muscle contraction, and moderate heat enhances both muscle and nerve sensitivity. However, moderate cold reduces the strength of contraction, and when temperatures drop below freezing, muscles significantly lose their responsiveness without necessarily becoming stiff.

While well supplied with blood, muscle will contract without fatigue, but if the blood supply is shut off, it soon loses its irritability and becomes rigid. The more a muscle is used in moderation the more it develops, but after it has done a certain amount of work it becomes exhausted, losing its irritability or power to respond to stimuli and later becoming rigid. Such fatigue is due to the production of certain poisonous waste products which have a paralyzing effect on the nerves and which are ordinarily gradually carried away in the blood, but which sometimes, if produced to excess, accumulate too fast for the blood wholly to remove them. Usually the nerve becomes exhausted first and the muscle substance later. So long as it is connected with the nervous [Pg 27] system a muscle will respond to stimuli, but when the nerve becomes tired, degeneration is more rapid. In fact, the degree of exhaustion is determined by several factors, as by relation to the central nervous system, variations in temperature, blood supply, and functional activity, the process being more rapid in warm than in cold blooded animals.

While well supplied with blood, muscle will contract without getting tired, but if the blood supply is cut off, it quickly loses its ability to respond and becomes stiff. The more a muscle is used moderately, the more it develops, but after a certain amount of work, it gets exhausted, losing its responsiveness to stimuli and later becoming rigid. This fatigue is caused by the buildup of certain toxic waste products that have a paralyzing effect on the nerves and are usually slowly removed by the blood, but sometimes, if produced in excess, they accumulate too quickly for the blood to eliminate them completely. Typically, the nerve gets exhausted first, and the muscle tissue follows. As long as a muscle is connected to the nervous system, it will respond to stimuli, but when the nerve gets tired, degeneration happens more quickly. In fact, the level of exhaustion is influenced by several factors, such as its relation to the central nervous system, changes in temperature, blood supply, and functional activity, with the process being faster in warm-blooded animals than in cold-blooded ones.

Cilia.—A few motions are accomplished by tissue that is not muscular, as in the case of the cilia attached to the cells of the respiratory tract, which lie flat on the free surface and then lash forward, serving in the air cells to keep the air in motion and in the tubes to send secretions from below upward and outward and to keep out foreign bodies. Cilia are also found in the female genital tract, where they aid the passage of the ovum from the ovary to the womb. They act together, though apparently not governed by the nervous system. As in the white corpuscles of the blood, whose motion also is not muscular, the changes that take place in ciliated epithelium are probably about the same as those in muscular tissue, that is, contractile.

Cilia.—A few movements are made by tissue that isn't muscular, like the cilia attached to the cells in the respiratory tract. These cilia lie flat on the surface and then whip forward, keeping the air in motion in the air cells and helping to move secretions from below upward and outward, as well as keeping out foreign particles. Cilia are also present in the female reproductive tract, where they help transport the egg from the ovary to the uterus. They work together, though they don't seem to be controlled by the nervous system. Similar to the white blood cells, whose movement is also non-muscular, the changes occurring in ciliated epithelium are likely similar to those in muscle tissue, meaning they are contractile.

The Blood.—To most of the tissues just described nourishment is brought in the blood, which circulates through the body in a system of hollow tubes, the arteries and veins, whence it is distributed through the agency of the lymphatic system. There are no blood-vessels, however, in the epidermis, epithelium, nails, hair, teeth, nor in the cornea of the eye. The vessels that carry the blood from the heart are called arteries, those that return it veins. The former begin as large vessels and gradually decrease in size; the latter begin as small vessels and form larger and larger trunks as they approach the heart.

The Blood.—For most of the tissues just mentioned, nourishment is supplied by the blood, which flows through the body in a network of hollow tubes known as arteries and veins, from which it is distributed through the lymphatic system. However, there are no blood vessels in the epidermis, epithelium, nails, hair, teeth, or the cornea of the eye. The vessels that carry blood away from the heart are called arteries, while those that return it are called veins. Arteries start as large vessels and gradually shrink in size; veins, on the other hand, start as small vessels and become larger trunks as they get closer to the heart.

The arteries have three coats: 1. a thin, serous coat, the internal or intima; 2. a middle or muscular coat, and 3. an external coat of connective tissue. The middle coat is the thickest and is the one that prevents the walls from collapsing when cut across. Except in the [Pg 28] cranium, each artery is enclosed in a sheath with its vein or veins, the venæ comites. Usually the arteries occupy protected situations and are straight in their course. Where a vessel has to accommodate itself to the movements of a part, however, it may be curved, as in the case of the facial artery which is curled on itself to allow for movements of the jaw. They anastomose or communicate freely with one another, thus promoting equality of distribution and pressure and making good circulation possible even after the obliteration of a large vessel.

The arteries have three layers: 1. a thin, serous layer, the inner or intima; 2. a middle or muscular layer, and 3. an outer layer of connective tissue. The middle layer is the thickest and keeps the walls from collapsing when cut. Except in the [Pg 28] skull, each artery is surrounded by a sheath along with its vein or veins, the venæ comites. Typically, arteries are in protected locations and run straight. However, when a vessel needs to adapt to the movements of a part, it can be curved, like the facial artery, which is twisted to allow for jaw movement. They connect or communicate easily with each other, promoting balanced distribution and pressure and enabling good circulation even if a large vessel gets blocked.

The veins have three coats like the arteries, but they are not so thick and the muscular coat is not so highly developed, so that the walls collapse when cut and have no elasticity. There are constrictions on the surface of many of the veins due to the presence of valves. These valves are formed of semilunar folds of the lining membrane and are arranged in pairs. They serve to prevent the blood, whose circulation in the veins is sluggish, from flowing back.

The veins have three layers just like the arteries, but they aren't as thick, and the muscle layer isn't as well-developed, so the walls collapse when cut and lack elasticity. Many veins have constrictions on their surface because of valves. These valves are made of half-moon shaped folds of the inner lining and are set up in pairs. They help stop the blood, which moves slowly in the veins, from flowing backward.

There are two sets of veins, the superficial and the deep, which communicate with each other. In fact, all the veins, large and small, anastomose very freely, especially in the skull and neck, where obstruction would result in serious trouble, throughout the spinal cord, and in the abdomen and pelvis. The deep veins accompany the arteries in their sheath, while the superficial ones have thicker walls and run between the layers of the superficial fascia under the skin, terminating in the deep veins. In the skull the venous channels take the form of sinuses, formed by a separating of the layers of the dura mater, with an endothelial lining that is continuous with that of the veins.

There are two types of veins: superficial and deep, which connect with each other. In fact, all veins, whether large or small, interconnect quite easily, especially in the skull and neck, where any blockage could cause serious issues, throughout the spinal cord, and in the abdomen and pelvis. The deep veins run alongside the arteries in their protective sheath, while the superficial veins have thicker walls and lie between the layers of the superficial fascia beneath the skin, eventually leading into the deep veins. In the skull, the venous channels are formed into sinuses, created by the separation of the layers of the dura mater, with a lining of endothelial cells that is continuous with that of the veins.

The capillaries are intermediate between the arteries and the veins, the final division of the arteries and the first source of the veins. They are tiny vessels with but a single coat, continuous with the innermost coat of both arteries and veins and consisting practically of one layer of cells with a small amount of connective tissue between. [Pg 29] They spread in a great network throughout the tissues, forming plexuses and being especially abundant where the blood is needed for other purposes than local nutrition, as in the secreting glands. Their diameter is so small that the red corpuscles have to pass in single file and may even then be squeezed out of shape. As they have no muscular tissue in their walls, they have no power of contracting. Their walls, however, like those of the smaller arteries and veins, are porous and by virtue of this quality they play an important part in the economy, since in them the exchange takes place between the tissues and the blood.

The capillaries are in between the arteries and veins, marking the end of the arteries and the start of the veins. They are tiny vessels with just one layer, continuous with the innermost layer of both arteries and veins, consisting mainly of one layer of cells with a small amount of connective tissue in between. [Pg 29] They create a vast network throughout the tissues, forming plexuses and are especially abundant where blood is needed for purposes other than local nutrition, like in the secreting glands. Their diameter is so small that red blood cells have to pass through in single file and may even get slightly squished. Since they lack muscular tissue in their walls, they can't contract. However, their walls, like those of the smaller arteries and veins, are porous, and because of this quality, they play a crucial role in the body's functions since it's here that the exchange between the tissues and the blood occurs.

The arteries in general carry freshly oxidized blood and the veins blood from which the oxygen has been largely used up and which contains waste material. In the pulmonary system, however, the case is reversed, the pulmonary arteries conveying venous blood, as it is called, from the heart to the lungs to be oxidized and the veins returning the blood after it has received its new supply of oxygen.

The arteries typically carry oxygen-rich blood, while the veins carry blood that has mostly used up its oxygen and contains waste. However, in the pulmonary system, this is reversed; the pulmonary arteries carry deoxygenated blood from the heart to the lungs to get oxygen, and the veins bring the blood back after it has picked up a fresh supply of oxygen.

The pumping of the blood through the arteries is assisted by the contractions of the muscular coat, while the elastic tissue, of which it contains a certain amount, gives elasticity to the walls and enables them to stretch and so to accommodate the larger blood supply forced into them at each beat by the heart. The walls of the veins have not the power of contracting and the blood is pushed through more by gravity and the action of the arteries than by any action of their own.

The pumping of blood through the arteries is aided by the contractions of the muscle layer, while the elastic tissue it contains gives the walls flexibility, allowing them to stretch and accommodate the larger volume of blood pushed into them with each heartbeat. The walls of the veins don’t have the ability to contract, so the blood is mainly moved along by gravity and the action of the arteries rather than any action from the veins themselves.

The walls of all the vessels are nourished by tiny blood-vessels in the outer coat, known as vasa vasorum, and the nerves that regulate the action of the arteries are the vasomotor nerves from the vasomotor center in the medulla. Sufficient impulse goes from this center to the blood-vessels all the time to keep them somewhat contracted, in a state of tone, that is, which is increased or diminished as the blood supply is to be diminished or increased. [Pg 30]

The walls of all the blood vessels are supplied with tiny blood vessels in the outer layer, called vasa vasorum, and the nerves that control how the arteries work are the vasomotor nerves coming from the vasomotor center in the brainstem. This center sends enough signals to the blood vessels constantly to keep them slightly contracted, in a state of tone, which can be increased or decreased depending on whether blood flow needs to be reduced or increased. [Pg 30]

Lymphatic System.—The lymphatic system also extends throughout the body and consists of a system of channels, spaces, and glands very closely related to the circulatory system and containing a fluid called lymph. There are three principal parts to the system: 1. the lymph spaces, which are open spaces, with no definite walls, in the connective tissue framework of the body, more frequent near arteries and veins and especially so among the capillaries; 2. the lymph capillaries or small vessels which connect the lymph spaces; and 3. the lymphatic vessels, of which there is a deep and a superficial set, the latter accompanying the superficial veins on the surface of the body, the former accompanying the deep blood-vessels. [Pg 31]

Lymphatic System.—The lymphatic system also runs throughout the body and consists of a network of channels, spaces, and glands that are closely related to the circulatory system and contain a fluid called lymph. The system has three main parts: 1. the lymph spaces, which are open areas, without defined walls, in the connective tissue framework of the body, more commonly found near arteries and veins and especially among the capillaries; 2. the lymph capillaries or small vessels that connect the lymph spaces; and 3. the lymphatic vessels, which include both a deep and a superficial set, the latter traveling alongside the superficial veins on the body's surface, while the former runs alongside the deep blood vessels. [Pg 31]

Fig. 7.—Diagram showing the course of the main trunks of the absorbent system: the lymphatics of lower extremities (D) meet the lacteals of the intestines (LAC) at the receptaculum chyli (R.C.), where the thoracic duct begins. The superficial vessels are shown in the diagram on the right arm and leg (S), and the deeper ones on the left arm (D). The glands are here and there shown in groups. The small right duct opens into the veins on the right side. The thoracic duct opens into the union of the great veins of the left side of the neck (T). (Yeo.)

Fig. 7.—Diagram showing the path of the main trunks of the absorbent system: the lymphatics of the lower extremities (D) connect with the lacteals of the intestines (LAC) at the receptaculum chyli (R.C.), where the thoracic duct begins. The superficial vessels are displayed in the diagram on the right arm and leg (S), while the deeper ones are on the left arm (D). The glands are illustrated here and there in groups. The small right duct opens into the veins on the right side. The thoracic duct opens into the junction of the major veins on the left side of the neck (T). (Yeo.)

The lymph spaces are generally small, though there are some large serous cavities, such as the abdomen, that may be considered as extended lymph spaces.

The lymph spaces are typically small, but there are some large fluid-filled cavities, like the abdomen, that can be seen as enlarged lymph spaces.

Fig. 8.—Diagram of a lymphatic gland, showing afferent (a. l.) and efferent (e. l.) lymphatic vessels; cortical substance (C); medullary substance (M); fibrous coat (c); sending trabeculæ (tr) into the substance of the gland, where they branch, and in the medullary part form a reticulum; the trabeculæ are surrounded by the lymph path or sinus (l. s.), which separates them from the adenoid tissue (l. h.). (Sharpey.)

Fig. 8.—Diagram of a lymph node, showing incoming (a. l.) and outgoing (e. l.) lymphatic vessels; outer layer (C); inner layer (M); fibrous covering (c); sending connective tissue strands (tr) into the node, where they branch and form a network in the inner part; the connective strands are surrounded by the lymph space or sinus (l. s.), which separates them from the glandular tissue (l. h.). (Sharpey.)

The lymphatic vessels have delicate, transparent walls, with three coats like the arteries, though much thinner, and anastomose even more freely than the veins. They have a beaded appearance due to the presence of numerous valves, which form constrictions on their surface. The right lymphatic duct, which is only about an inch long, drains all the lymphatics of the right half of the upper part of the trunk, the head, and the neck approximately, while the thoracic duct drains those of the rest of the body. The latter, which is the largest vessel of the [Pg 32] system, begins opposite the second lumbar vertebra with a bulb-like reservoir for the lymph or chyle, the receptaculum chyli, and extends up along the spinal column for a distance of about eighteen inches to the seventh cervical vertebra, where, with the right lymphatic duct, it empties into the left subclavian vein at its junction with the internal jugular, thus establishing direct communication between the lymph spaces and the venous system. The orifices of both vessels are guarded by semilunar valves to prevent regurgitation of the blood.

The lymphatic vessels have thin, transparent walls with three layers like arteries, but they are much thinner and connect more freely than veins. They look beaded because of the many valves that create constrictions on their surface. The right lymphatic duct, which is only about an inch long, drains all the lymphatics from the right side of the upper trunk, head, and neck, while the thoracic duct drains the rest of the body. The thoracic duct, the largest vessel in the [Pg 32] system, starts near the second lumbar vertebra with a bulb-like reservoir for lymph or chyle called the receptaculum chyli and extends along the spinal column for about eighteen inches to the seventh cervical vertebra. There, it empties into the left subclavian vein at its junction with the internal jugular, creating a direct connection between the lymph spaces and the venous system. Both vessels have semilunar valves at their openings to stop blood from flowing backward.

Fig. 9.—Central (superficial) lymphatic glands of the axilla. (After Leaf.)

Fig. 9.—Central (superficial) lymph nodes of the armpit. (After Leaf.)

The lymphatic glands are small oval glandular bodies and occur here and there along the course of the lymphatics. Before entering one of them the vessel breaks up into several afferent vessels which form a plexus within and then emerge again as several efferent vessels which soon unite to form one trunk. These glands occur chiefly in the mesentery, along the great vessels, and in the mediastinum, axilla, neck, elbow, groin, and popliteal space.

The lymphatic glands are small oval glands found at various points along the lymphatic system. Before entering one of these glands, the vessel splits into several afferent vessels that create a network inside and then exit as several efferent vessels that soon come together to form a single trunk. These glands are mainly located in the mesentery, near the large blood vessels, and in the mediastinum, axilla, neck, elbow, groin, and popliteal area.

The lymph varies in character with the locality, being a little thicker and more opalescent in the lacteals, as the lymphatics of the [Pg 33] small intestine are called, especially during digestion, when fat is present. Here it is called chyle. Otherwise it is generally a clear, transparent and slightly opalescent fluid, which, owing to the presence of fibrin, clots when drawn from the body and allowed to stand. In fact, it resembles blood plasma very closely in composition and, as it also contains a certain number of corpuscles or leucocytes that just correspond to the white corpuscles of the blood, it is practically blood without the red corpuscles. These leucocytes have considerable power of amœboid movement and are thought by some to play an important part in the absorption of food.

The lymph varies in its characteristics depending on the location, being a bit thicker and more milky in the lacteals, which are the lymphatic vessels of the [Pg 33] small intestine, especially during digestion when fat is present. This is referred to as chyle. Otherwise, lymph is generally a clear, transparent, and slightly milky fluid that, due to the presence of fibrin, clots when taken from the body and left to sit. In fact, it closely resembles blood plasma in composition and, since it also contains a certain number of cells or leucocytes that correspond to the white blood cells, it is essentially blood without the red blood cells. These leucocytes have a strong ability to move amoebically and are thought by some to play a significant role in food absorption.

Owing to intracapillary pressure, the lymph transudes into the lymph spaces and bathes the tissues, being carried away again by the lymphatics. The amount of transudation is determined by the blood pressure—the greater the pressure, the greater the amount of transudation—and is increased by some organic action of the cells in the walls of the vessels. In the process of transudation a certain amount of solid matter goes through the wall of the vessel and it is probable that certain protein elements can be carried thus from the blood-vessels to the lymphatics, though they do not pass through the capillary wall as readily as other substances. Some lymph is also probably formed by the action of the tissues themselves, though the process is not understood.

Due to intracapillary pressure, lymph seeps into the lymph spaces and surrounds the tissues, and is then transported away by the lymphatic vessels. The amount of this seepage is influenced by blood pressure—the higher the pressure, the more seepage occurs—and is increased by some organic activity of the cells in the walls of the vessels. During this seepage, a certain amount of solid material passes through the vessel wall, and it's likely that some protein elements are transferred from the blood vessels to the lymphatics, although they do not pass through the capillary wall as easily as other substances. Some lymph is also likely produced by the tissues themselves, though the exact process is not well understood.

All muscular movements, active or passive, including the respiratory movements, tend to drive the lymph on its way by pressure, the valves of the vessels keeping it from flowing back. Moreover, its flow is from the capillaries to the veins or from a region of high pressure to one of less pressure. There is probably also some contraction in the walls of the vessels themselves, and the continual formation of lymph helps to drive it along. If an obstruction to the circulation occurs, however, back-pressure results and causes too great transudation. In that event a limb becomes swollen, pale, and generally cool. It pits on [Pg 34] pressure, the pressure driving the lymph out and there being no circulation to bring it back. This condition is called œdema and occurs in liver, kidney, and heart troubles, being generally first observed at the ankles. In ascites, hydrothorax, hydrocephalus, and pericardial and pleural effusions the fluid corresponds to lymph in its composition and the large amount is due to excessive formation of the fluid, which is normally present in small quantities.

All muscle movements, whether active or passive, including breathing, help push lymph along by creating pressure, while the valves in the vessels prevent it from flowing backward. The lymph moves from the capillaries to the veins, essentially traveling from areas of high pressure to areas of lower pressure. There may also be some contraction in the walls of the vessels themselves, and the ongoing production of lymph helps propel it forward. However, if there’s an obstruction in circulation, it can lead to back pressure that causes excessive fluid to leak out. This can result in a limb becoming swollen, pale, and usually cool. It will leave an indentation when pressed, as the pressure forces the lymph out and there’s no circulation to return it. This condition is known as edema and can occur in liver, kidney, and heart problems, often first noticed at the ankles. In conditions like ascites, hydrothorax, hydrocephalus, and pericardial and pleural effusions, the fluid is similar to lymph in its makeup, with large amounts resulting from an overproduction of fluid that usually exists in smaller amounts.

Lymph gives the tissues substances from the blood that they need and carries off those they do not, whether waste or substances of use to other tissues. Because they thus absorb certain materials not needed by the tissues and convey them to the circulation, the lymphatics have also been called absorbents. Indeed, lymph may be spoken of as the middleman between the blood and the tissues.

Lymph provides tissues with essential substances from the blood and removes what they don't need, whether it's waste or materials that other tissues can use. Because they take in specific materials that aren’t needed by the tissues and transport them into the bloodstream, the lymphatics are also referred to as absorbents. In fact, lymph can be described as the intermediary between the blood and the tissues.

Another function of the lymph is to lubricate. Thus, the synovial fluid of the joints is lymph and the pleuræ and the pericardium contain lymph or serum to reduce the friction between the adjoining surfaces as much as possible. The brain and spinal cord do not quite fill the cavities of the cranium and the spinal column but float on a cushion of lymph, the cerebro-spinal fluid. When the brain, which is subject to increase and diminution in size, increases in size, it drives the lymph out, and when it diminishes, the lymph returns.

Another role of lymph is to provide lubrication. Therefore, the synovial fluid in the joints is made up of lymph, and the pleura and pericardium contain lymph or serum to minimize friction between the surfaces as much as possible. The brain and spinal cord don't completely fill the spaces in the skull and spinal column but float on a cushion of lymph, known as cerebrospinal fluid. When the brain, which can expand and shrink in size, gets larger, it pushes the lymph out, and when it shrinks, the lymph flows back in.

The lymph glands serve as a protection to adjacent parts and when it leaves the gland the lymph is purer and richer in leucocytes than when it entered. In fact, they filter harmful matter from the lymph and apparently also form white corpuscles. Normally they can with difficulty be felt, but in disease, if the leucocytes are unable to destroy or carry off the poison, the lymph carries it along to the glands, which swell and become tender. If the infection is not severe the swelling goes down and the tenderness passes after a short time, but if it is severe, there may be suppuration and abscess formation and [Pg 35] the gland even perhaps be destroyed, giving its life for the health of the part. Thus a wound in the foot, if infected, may cause irritation and enlargement of the glands at the knee and in the groin.

The lymph glands act as a protective barrier for nearby areas, and when lymph leaves the gland, it is cleaner and richer in white blood cells than when it entered. In fact, they filter out harmful substances from the lymph and also seem to produce white blood cells. Normally, they are hard to feel, but during illness, if the white blood cells can't eliminate or remove the poison, the lymph transports it to the glands, causing them to swell and become sore. If the infection isn't severe, the swelling and soreness will go down after a short time, but if it is severe, it can lead to pus formation and abscesses, and the gland may even be destroyed, sacrificing itself for the health of the surrounding area. For instance, an infected wound in the foot can lead to irritation and swelling of the glands in the knee and groin.

The lymphatic glands are frequently the seat of tubercular infection, especially in the neck, and are enlarged in scarlet fever, tonsillitis, and diphtheria. In syphilis there is general glandular enlargement, and the glands in the groin become enlarged in all diseases of the genital organs. In malignant growths, such as cancer, the extension of the disease is often along the lines of the lymphatics.

The lymph nodes often get infected with tuberculosis, particularly in the neck, and they swell during scarlet fever, tonsillitis, and diphtheria. In syphilis, there is a general swelling of the lymph nodes, and those in the groin become enlarged in any diseases affecting the genital organs. In cancers, the spread of the disease often follows the pathways of the lymphatic system.

Glands.—Of glands in general a word might now be spoken. They are of two kinds, excreting and secreting, and, when simple, are formed by the folding in of a free surface, as in the case of the salivary, gastric, and sebaceous glands, the cells at the gland becoming so modified as to be able to perform the function of excreting or secreting. In racemose glands the gland is broken up into many pockets. Excreting glands take from an organ or from a part substances which have outlived their usefulness and are to be cast out of the body, while the secreting glands form from the blood substances that did not exist in it before, but which are of use to the body, as the ptyalin of the saliva. A strict line cannot, however, be drawn between the two kinds of glands, most glands partaking more or less of both functions, though the sebaceous and sweat glands are probably purely excreting glands and the salivary glands are almost purely secreting. The glands, moreover, are more or less interchangeable in their functions, that is, they have vicarious function, and one gland can take up and do for another what that other is for some reason unable to do. In jaundice, where there is stoppage of the bile duct, the kidneys help out the liver by excreting the bile. If one kidney is removed the other does work for both, and the glands of the skin may help out the kidneys or vice versa. Hemorrhage from the lungs sometimes occurs in suppression of the menses. [Pg 36]

Glands.—Let's talk about glands in general. They come in two types: excreting and secreting. When simple, they form through the folding in of a free surface, like the salivary, gastric, and sebaceous glands. The cells in these glands change to perform the roles of either excreting or secreting substances. In racemose glands, the gland is divided into many pockets. Excreting glands remove substances from an organ or part that are no longer useful and need to be eliminated from the body, while secreting glands make new substances from the blood that weren’t there before but are beneficial, like ptyalin in saliva. However, it’s hard to clearly differentiate between the two types, as most glands perform functions of both kinds to some extent. The sebaceous and sweat glands are likely purely excreting, while salivary glands are mostly secreting. Additionally, glands can often interchange their functions; that is, they can step in for one another when needed. For example, in jaundice, when the bile duct is blocked, the kidneys assist the liver by excreting bile. If one kidney is removed, the other can compensate for both, and the skin glands can also help the kidneys or vice versa. Sometimes, hemorrhage from the lungs occurs when there's a suppression of menstruation. [Pg 36]

In a general way the function of glands is chemical. They filter out by osmosis, selecting the useful parts for secretion and the useless for excretion. In the chemical action that goes on considerable energy is given off, as is shown by the amount of pressure in the glands and by the fact that their temperature is higher than that of the blood. They all work in a reflex manner, being under the control of the central nervous system. Thus, what is eaten affects the nerve terminals in the mouth, the sensation passes to the nervous system, and an impulse is carried by the motor nerves to the salivary glands.

In general, the function of glands is chemical. They filter out useful substances for secretion through osmosis, while eliminating the useless ones through excretion. This chemical process releases a significant amount of energy, evidenced by the pressure within the glands and the fact that their temperature is higher than that of the blood. They all operate reflexively, controlled by the central nervous system. Therefore, what we eat influences the nerve endings in the mouth, the sensation is transmitted to the nervous system, and an impulse is sent via motor nerves to the salivary glands.

Most of the glands have ducts to convey away their secretion to other parts of the body or to send excretions out of the body, but there are also ductless glands, which, though they seem to have some important function in the process of metabolism, are not well understood. Most of them seem to manufacture some substance that is absorbed by the tissues and that plays an important part in the bodily metabolism, though nothing is secreted by them externally. They are said to have an internal secretion, whereas the glands with ducts have an external secretion. The liver has both forms of secretion, the bile which is sent out and the glycogen that is stored. The ductless glands are the thymus and thyroid glands, the suprarenal capsules, and the pituitary body in the brain.

Most glands have ducts that transport their secretions to other parts of the body or excrete waste outside the body, but there are also ductless glands that, while they seem to have important roles in metabolism, are not very well understood. Most of these glands appear to produce substances that are absorbed by the tissues and play a crucial role in the body's metabolism, even though they don’t release anything externally. They are said to have internal secretion, while the glands with ducts have external secretion. The liver produces both types of secretion: bile, which is excreted, and glycogen, which is stored. The ductless glands include the thymus and thyroid glands, the adrenal glands, and the pituitary gland in the brain.

Nervous Tissue.—Presiding over all the organs, muscles, and blood-vessels, as the source of all action and all sensation, are the nerves. Nervous tissue is of two kinds: 1. the gray or vesicular, which originates impulses and receives impressions, and 2. the white or fibrous, which conveys impressions. The gray matter consists of large granular cells of protoplasm containing nuclei, which give off many branches or dendrites. From the under surface there usually comes one main branch, the axis-cylinder process. These processes sometimes [Pg 37] give off branches and sometimes not, but they form the nerve fibers and carry impulses away from the nerve cells. The cells of the processes are elongated in shape, have a nucleus, and are placed end to end, with a definite constriction between them.

Nervous Tissue.—Controlling all the organs, muscles, and blood vessels, and serving as the source of all action and sensation, are the nerves. Nervous tissue comes in two types: 1. the gray or vesicular, which generates impulses and receives sensations, and 2. the white or fibrous, which transmits sensations. The gray matter is made up of large granular cells of protoplasm that contain nuclei and extend many branches called dendrites. Typically, one main branch, the axis-cylinder process, emerges from the underside. These processes sometimes branch off, but they usually do not, forming nerve fibers that carry impulses away from the nerve cells. The cells of the processes are elongated, have a nucleus, and are aligned end to end, with a clear constriction between them.

Each axis-cylinder process is surrounded by a sheath called the medullary sheath, while each nerve fiber consists of a central axis-cylinder process surrounded by the white substance of Schwann and enclosed in a sheath. A bundle of these fibers invested in a fibro-areolar membrane called the neurilemma constitutes a nerve, and of these the white matter is formed. The blood supply is brought by minute vessels, the vasa nervorum.

Each axis-cylinder process is surrounded by a sheath called the medullary sheath, while each nerve fiber consists of a central axis-cylinder process wrapped in the white substance of Schwann and enclosed in a sheath. A bundle of these fibers covered in a fibro-areolar membrane called the neurilemma makes up a nerve, and the white matter is formed from these. The blood supply is delivered by tiny vessels, the vasa nervorum.

Fig. 10.—Longitudinal nerve fiber (diagrammatic): a, Axis-cylinder; b, medullary sheath; c, neurilemma; d, nucleus; e, node of Ranvier. (Leroy.)

Fig. 10.—Longitudinal nerve fiber (diagrammatic): a, axis cylinder; b, myelin sheath; c, neurilemma; d, nucleus; e, node of Ranvier. (Leroy.)

The nerves of the cerebro-spinal system preside over animal life and have to do with voluntary acts, while those from the sympathetic system regulate organic life and are quite independent of the will. Both sensory and motor nerves extend all over the body, accompanying the arteries in a general way. The sensory nerves end on the surface in plexuses, in end bulbs situated in the papillæ of the skin, or in tactile corpuscles, these last occurring more especially where there is no hair. The motor nerves end peripherally in plexuses or by end plates. The central terminations of the motor nerves and the terminations of sensory nerves in special organs, except where they end in a cell, are not well understood.

The nerves of the central nervous system control animal behavior and are involved in voluntary actions, while the nerves from the sympathetic system manage bodily functions and work independently of our will. Both sensory and motor nerves spread throughout the body, generally following the arteries. The sensory nerves terminate at the surface in networks, at end bulbs located in the skin's papillae, or in tactile corpuscles, especially where there's no hair. The motor nerves end at the periphery in networks or at nerve endings. The central connections of the motor nerves and the connections of sensory nerves in specialized organs, except where they connect to a cell, aren’t well understood.

Like muscles, nerves are probably never at rest, for through them the muscles get their tone. When a nerve acts, no heat is produced and there is no change in the nerve afterward, as there is in muscle. Probably nerve impulse is the transmission of physical rather than [Pg 38] chemical changes along the fiber, the atoms of the nerve being set in vibration and the vibrations being transmitted along its length. Stimulation is produced by physical injury, by chemical influence, by electricity, by heat, and the message is always referred to the nerve termination. Thus, if the nerve at the elbow, over the “crazy bone,” is touched, a tingling is felt in the fingers rather than at the point of pressure. A person who has had an arm or leg amputated will frequently speak of his fingers or toes on that side being cold, or complain of pain in them, because the scar below the point of amputation tightens around the nerves and pinches them.

Like muscles, nerves are probably never at rest, because they give muscles their tone. When a nerve activates, it doesn't produce heat and doesn't change afterward, unlike muscle. Nerve impulses likely involve the transmission of physical, not chemical, changes along the fiber; the atoms in the nerve vibrate, and these vibrations travel along its length. Stimulation happens due to physical injury, chemical effects, electricity, or heat, and the message always goes to the nerve ending. So, when the nerve at the elbow, over the "funny bone," is touched, you feel a tingling in your fingers instead of at the point of pressure. A person who has had an arm or leg amputated might often say their fingers or toes on that side feel cold or complain of pain in them because the scar below the amputation tightens around the nerves and pinches them.

It is through the nerves that people get in touch with the outer world and that they judge of size, weight, etc. All careful adjustment of the muscles is under the control of the nervous system.

It’s through the nerves that people connect with the outside world and assess size, weight, and so on. The precise regulation of the muscles is managed by the nervous system.


CHAPTER II.
THE SKIN, ITS ACCESSORIES
AND ITS FUNCTION.

The whole exterior surface of the body is covered by the skin, an excreting and absorbing organ, which serves as a protection to the parts beneath and is also the organ of touch. It has two layers, a superficial and a deep. The superficial layer, the epidermis or cuticle, is composed wholly of epithelial cells, of which the deepest layer is columnar and moulded upon the papillary layer of the derma, while the intermediate layers are more rounded and the surface ones flat. The deepest layer also contains the skin pigment, which causes the variation in shade between the Indian, the negro, and the white man. Below the epidermis, which is chiefly protective, is the tough, elastic, and flexible tissue of the derma or true skin, in which are vested most of the activities of the skin. Its surface is covered with papillæ, which are more numerous in the more sensitive parts. Each papilla contains one or more capillary loops and one or more nerve fibers, while some terminate in an oval body known as a tactile corpuscle. Beneath the papillæ is the reticular layer, composed of interlacing bands of fibrous tissue and containing blood-vessels, lymphatics, and nerves, as well as unstriped muscle fibers where hair is present.

The entire outer surface of the body is covered by the skin, an organ that both excretes and absorbs, serving to protect the underlying parts and functioning as the sense of touch. It has two layers: a superficial layer and a deep layer. The superficial layer, the epidermis or cuticle, is made entirely of epithelial cells, with the deepest layer being columnar and shaped over the papillary layer of the derma, while the middle layers are more rounded and the outermost ones are flat. The deepest layer also contains skin pigment, which leads to the differences in skin tone among Indians, blacks, and whites. Beneath the epidermis, which mainly acts as protection, lies the tough, elastic, and flexible tissue of the dermis or true skin, where most of the skin's functions take place. Its surface is covered with papillae, which are more abundant in sensitive areas. Each papilla contains one or more capillary loops and one or more nerve fibers, with some ending in an oval structure known as a tactile corpuscle. Below the papillae is the reticular layer, made up of interwoven bands of fibrous tissue and containing blood vessels, lymphatics, and nerves, as well as smooth muscle fibers where hair is found.

Fig. 11.—Vertical section of skin.

Fig. 11.—Vertical skin section.

[Pg 40] At the apertures of the body the skin stops and is replaced by mucous membrane, an integument of greater delicacy but which consists fundamentally of the same two layers, a superficial, bloodless epithelium and a deep fibrous derma. It is continuous with the skin, but is much redder and more sensitive and bleeds more easily. The passages and cavities that it lines, unlike those lined by serous membranes, communicate with the exterior of the body and are for that reason protected against contact with foreign substances by mucus, which is thicker and more sticky than the lymph that moistens the endothelium found on serous surfaces. Mucous membrane is found in the alimentary canal, the respiratory tract, and the genito-urinary tract. In cavities, like the stomach and intestines, which are subject to variations in capacity, it is thrown into folds or rugæ. The mucus is secreted by small glands in the membrane.

[Pg 40] At the openings of the body, the skin ends and is replaced by mucous membrane, a more delicate covering that still consists of the same two layers: a thin, bloodless surface layer and a deeper fibrous layer. It's continuous with the skin, but it appears redder, is more sensitive, and tends to bleed more easily. The passages and cavities it lines, unlike those covered by serous membranes, connect to the outside of the body and are therefore protected from foreign substances by mucus, which is thicker and stickier than the lymph that moistens the endothelium on serous surfaces. Mucous membrane is present in the digestive tract, the respiratory system, and the urinary and reproductive tracts. In areas like the stomach and intestines, which can change shape, it forms folds or rugæ. The mucus is produced by small glands within the membrane.

Appendages of the Skin.—The skin has various appendages. On the dorsal surface of the last phalanges of the fingers and toes are flattened and horny modifications of epithelium, the nails. They have a root embedded in a groove of skin by which they grow in length and a vascular matrix of derma beneath them which gives growth in thickness. To their growth in length there seems to be no limit.

Appendages of the Skin.—The skin has different appendages. On the top surface of the last bones of the fingers and toes are flattened and hard modifications of skin, known as nails. They have a root that is located in a groove of skin, which allows them to grow longer, and there is a layer of blood vessels beneath them that contributes to their thickness. There appears to be no limit to their length growth.

The hairs also, which occur all over the body, except on the palms of the hands and the soles of the feet, are a modification of the epithelium. Each hair has a bulbous root springing from an involution in the epidermis and derma called the hair follicle, into which one or two sebaceous glands empty. It is raised by involuntary muscle fibers and grows by constant additions to the surface by which it is attached. This growth seems, however, to be limited, and when its term [Pg 41] is reached the hair falls out and is replaced by another. The horny epithelial cells that go to form the hair contain the pigment that gives it its color.

The hairs, which are found all over the body except on the palms of the hands and the soles of the feet, are a variation of the epithelium. Each hair has a bulbous root that comes from an inward fold in the epidermis and dermis called the hair follicle, into which one or two sebaceous glands empty. It is lifted by involuntary muscle fibers and grows through constant additions to the surface it's attached to. This growth, however, appears to be limited, and once it reaches its limit, the hair falls out and is replaced by a new one. The hard epithelial cells that make up the hair contain the pigment that gives it its color.

Fig. 12.—Skin and longitudinal section of hair: a, Epidermis; b, corium; c, sebaceous gland; d, fibrous root-sheath; e, glassy membrane; f, outer root-sheath; g, inner root-sheath; h, expanded bulbous end of hair; i, papilla of hair; j, arrector pili; k, adipose tissue. (Leroy)

Fig. 12.—Skin and longitudinal section of hair: a, Epidermis; b, dermis; c, sebaceous gland; d, fibrous root sheath; e, glassy membrane; f, outer root sheath; g, inner root sheath; h, expanded bulbous end of hair; i, hair papilla; j, arrector pili muscle; k, fat tissue. (Leroy)

Like the hairs, the sebaceous glands are situated in all parts of the body except the palms of the hands and the soles of the feet. They lie in the papillary layer and empty into the hair follicles, except occasionally, when they empty directly upon the surface of the skin. They secrete an oily substance, sebum, the débris resulting from the degeneration of the epithelial cells of the gland itself, which serves to keep the hair glossy and the skin soft and flexible. [Pg 42]

Like hair, the sebaceous glands are found all over the body, except on the palms of the hands and the soles of the feet. They are located in the papillary layer and usually release into hair follicles, although sometimes they release directly onto the skin's surface. They produce an oily substance called sebum, which is made from the breakdown of the gland's epithelial cells and helps keep the hair shiny and the skin soft and flexible. [Pg 42]

The sweat glands, on the other hand, are more frequent on the palms and soles and though sometimes found in the derma are usually situated lower down in the subcutaneous cellular tissue. They are least numerous on the back and neck. Coiled up in the lower layers of the skin, they discharge the sweat through a spiral excretory duct upon its free surface.

The sweat glands, on the other hand, are more common on the palms and soles and while they can sometimes be found in the dermis, they're usually located deeper in the subcutaneous tissue. They are least common on the back and neck. Located in the lower layers of the skin, they release sweat through a spiral excretory duct onto the surface.

The sweat is a clear, colorless, watery fluid with a salty taste, an alkaline reaction, and a characteristic odor that varies with the individual. If very scanty, it may be acid in reaction. Besides water it contains a small percentage of solids, as inorganic salts, especially sodium chloride, fatty acids, neutral fats, and at times, especially in some diseases of the kidneys, urea, that is, the end-products of the metabolism of starches and fats chiefly. There is usually also some carbon dioxide, whence the expression cutaneous respiration.

The sweat is a clear, colorless, watery fluid that tastes salty, has an alkaline reaction, and a distinct smell that changes from person to person. If it's very minimal, it can be acidic. Along with water, it contains a small amount of solids, like inorganic salts, particularly sodium chloride, fatty acids, neutral fats, and sometimes, especially in certain kidney diseases, urea, which are the end-products of metabolizing starches and fats mainly. There's usually some carbon dioxide as well, which is why we refer to it as cutaneous respiration.

The sweat serves to keep the skin moist and in good condition, to remove outworn and poisonous or irritating matters, and to regulate the temperature. As a rule it evaporates upon reaching the surface, in which case it is known as invisible or insensible perspiration, but if conditions of the atmosphere are not favorable to prompt evaporation, as when the air is damp, the skin becomes damp and there is visible perspiration.

The sweat keeps the skin hydrated and healthy, helps eliminate waste and harmful substances, and regulates body temperature. Usually, it evaporates as it reaches the skin's surface, which is called invisible or insensible perspiration. However, if the atmosphere isn't ideal for quick evaporation, like when it's humid, the skin gets wet, and you can see the sweat.

Though an abundant supply of blood increases the action of the sweat glands, they are regulated by definite secretory nerves rather than by the vasomotor nerves. In a cold sweat the action is probably due to some disturbance of the nerve supply without increase of the blood supply. Ordinarily perspiring is a reflex act due to the stimulation of the afferent cutaneous nerves, as by the application of heat, but sometimes, as in cases of strong emotions, involuntary impulses are sent from the brain to the spinal centers and so arouse the action of the glands. Atropin has the power of preventing the secretion of sweat [Pg 43] by paralyzing the terminations of the secretory nerves, while pilocarpin produces an opposite effect in a similar way.

Although having a lot of blood increases the activity of sweat glands, they’re controlled by specific secretory nerves instead of vasomotor nerves. In the case of a cold sweat, the response is likely caused by some disruption in the nerve supply without an increase in blood flow. Usually, sweating is a reflex action triggered by stimulating the sensory nerves in the skin, such as with heat, but sometimes, like during intense emotions, involuntary signals are sent from the brain to the spinal cord, which then activates the glands. Atropine can stop sweating by blocking the endings of the secretory nerves, while pilocarpine does the opposite by activating them. [Pg 43]

On account of these sweat glands the skin becomes next in importance after the kidneys in the excretion of waste products. The quantity of sweat excreted varies greatly and is hard to measure. It is influenced by the temperature and humidity of the surrounding air, by the nature and quantity of food and drink consumed, by the amount of exercise, the relative activity of other organs, especially the kidneys, and by certain mental conditions. The hotter it is, the greater the amount of perspiration. In damp weather there may be less perspiration, but it does not evaporate and is therefore more in evidence.

Due to these sweat glands, the skin becomes the second most important organ after the kidneys for getting rid of waste products. The amount of sweat produced varies widely and can be difficult to measure. It is affected by the temperature and humidity of the air, the type and amount of food and drink consumed, the level of physical activity, the relative function of other organs, especially the kidneys, and certain mental states. The hotter it gets, the more you sweat. In humid weather, you might sweat less, but it doesn’t evaporate as easily, making it more noticeable.

Ordinarily man has a temperature of 98.6°. The source of this body heat or temperature is the general body metabolism, muscular activity, and activity of the glands, especially of the liver, which is constantly active, the blood in the hepatic vein being warmer than that in any other part of the body. The tissue of the brain also is said to be warmer than the surrounding blood, and the heart and respiratory muscles, which are in constant activity, are responsible for much of the body heat. The amount of heat generated in the body, therefore, varies at different times, according as a person is awake or asleep, quiet or active.

Typically, a person has a temperature of 98.6°F. This body heat comes from general metabolism, muscle activity, and gland activity, especially in the liver, which is always working hard. The blood in the hepatic vein is warmer than in any other part of the body. It's also said that the brain tissue is warmer than the blood around it, and the heart and breathing muscles, which are always active, contribute significantly to body heat. So, the amount of heat produced in the body varies at different times depending on whether a person is awake or asleep, calm or active.

Temperature Regulation.—The temperature is regulated by variations in the production and loss of heat, less being known of its production than of its loss. It has been calculated that four-fifths of the energy of the body is converted into heat, one-fifth into work. As the minimum amount of heat produced in twenty-four hours is sufficient to raise 10 gallons of water from 0° to boiling-point, it is evident that if there were not some way for the escape of much of this heat the body would become hotter and hotter and finally destroy itself. The temperature, however, except on the surface, is uniform, heat being [Pg 44] lost as fast as it is produced. For, although oxidation at any point raises the heat of the blood at the point, this heat is carried by the blood to other parts, to which the surplus is given up, while blood cooled in the skin goes to the hotter inward parts to cool them and be warmed itself. In fact, heat is expended by conduction and radiation, through respiration, perspiration, and heat given to the urine and fæces. It is, therefore, largely, 75 to 80 per cent., carried off through the skin and the lungs; 60 to 70 per cent. is lost by radiation to the air and other bodies with which the body comes in contact; 20 to 30 per cent. is lost by the evaporation of sweat, 4 to 8 per cent. by the warming of expired air, urine and feces, and 1 to 2 per cent. by cold food that is taken in. Radiation acts more favorably where the surroundings are cool and the air in motion, as on a breezy day. Conduction is carried on best where the surrounding air is cool, especially if it is moist, for moist air is a better conductor of heat than dry air. Evaporation is very important in hot weather or where men work in hot air.

Temperature Regulation.—The body regulates its temperature through changes in heat production and loss, with less being understood about how heat is produced than how it's lost. It's estimated that 80% of the body's energy is turned into heat, while 20% is used for work. The least amount of heat generated in a 24-hour period is enough to raise 10 gallons of water from 0° to boiling, which shows that if there weren't ways for the body to lose excess heat, it would get hotter and eventually harm itself. The temperature inside the body, except for the surface, remains consistent, as heat is lost as quickly as it's made. While oxidation raises the temperature of blood in specific areas, that heat is circulated to cooler parts of the body, while the cooler blood returning from the skin helps cool the warmer internal organs. Heat is lost through conduction, radiation, breathing, sweating, and in the urine and feces. About 75 to 80 percent of heat is expelled through the skin and lungs; 60 to 70 percent is lost through radiation to the air and other surfaces nearby; 20 to 30 percent is lost through sweat evaporation; 4 to 8 percent is lost when exhaling warm air, urine, and feces, and 1 to 2 percent comes from consuming cold food. Radiation is more effective in cooler environments with moving air, like on a breezy day. Conduction works best in cooler, especially moist, air since moist air conducts heat better than dry air. Evaporation is crucial in hot weather or when people are working in high temperatures.

Even in health the temperature may range from 98.6° to 99.5°, and a degree or two below or above is not dangerous. When a person first gets up in the morning his temperature is apt to be subnormal, but after food and exercise have been taken it becomes normal and stays so till the end of the day, when, if the person is tired, it may go up a little. If a person is tired out, the temperature is apt to be subnormal. There is also in the body what is called the vital tide, which is highest afternoon and evening and lowest in the morning.

Even when a person is healthy, their body temperature can range from 98.6° to 99.5°, and being a degree or two above or below that isn’t harmful. Typically, when someone first gets out of bed in the morning, their temperature tends to be lower than normal, but after eating and moving around, it usually returns to normal and remains stable until the end of the day, when it might rise slightly if the person is tired. When someone is completely worn out, their temperature is likely to be lower than normal. The body also experiences what’s known as the vital tide, which peaks in the afternoon and evening and is at its lowest in the morning.

The rate of production of heat varies greatly in different people. One person uses a certain amount of tissue more quickly than another, that is, he lives faster. Moreover, size makes a difference in that a small body has more surface to its weight than a large one and so has to produce the same amount of heat at a faster rate in order to maintain the right temperature. Taking food increases heat, probably because of [Pg 45] the muscular effort needed to eat it. Muscular work is another factor. And finally the whole matter of heat production seems to be under the control of the nervous system. Not much is known on this point except that there is a heat center in the medulla which plays an important part in heat production and whose influence is seen where the temperature shoots way up in disease just before death. It is now thought that fever is due to a disturbance of this nervous mechanism, though just what the disturbance is is not known.

The rate at which people produce heat varies a lot. Some individuals use certain tissues faster than others, meaning they have a higher metabolic rate. Additionally, size matters because smaller bodies have more surface area relative to their weight than larger ones, so they need to generate the same amount of heat more quickly to maintain their temperature. Eating food increases heat production, likely due to the energy required for the muscular effort involved in eating. Muscular activity is another key factor. Ultimately, the whole process of heat production seems to be regulated by the nervous system. There's not much known about this, except that there's a heat center in the medulla that plays a crucial role in producing heat, and its influence can be seen when body temperature spikes in illness just before death. It is currently believed that fever results from a disruption of this nervous system mechanism, although the exact nature of the disruption isn’t clear.

Fever is a condition of increased bodily temperature, due to increased production or to decreased loss of heat. As a rule, in all fevers the metabolic changes in the body are increased. Hence the patient becomes emaciated in a long fever. The frequent increase in the amount of urea during fever shows an increase in protein metabolism. The temperature in fevers rises as high as 106° and in sunstroke sometimes to 110°. Except in sunstroke a higher temperature than 106° generally means death. Subnormal temperature is due to a decrease in the bodily metabolism and so to lessened heat production. As a rule, if the functions are all active, especially that of the sweat glands, a person can be exposed to severe heat without the temperature being affected, though sometimes on a hot summer day it may be up half to one degree. The cause of heat-stroke with its high fever is unknown, but probably it is due to some effect on the heat center in the brain. Heat prostration is also due to prolonged exposure to heat, but is generally accompanied by a subnormal temperature. The effect of cold, as in freezing, is to diminish all the metabolic activities of the body. The temperature can be artificially regulated more or less by variations of food, varying amounts of exercise, by drugs, etc.

Fever is a condition where the body temperature rises, caused by either increased heat production or decreased heat loss. Generally, during any fever, the body's metabolic processes speed up. As a result, a person can become very thin if the fever lasts a long time. The noticeable rise in urea levels during a fever indicates heightened protein metabolism. Fever temperatures can reach as high as 106°F and even 110°F in cases of sunstroke. Except for sunstroke, a temperature higher than 106°F typically indicates a risk of death. Low body temperature occurs when metabolic activity decreases, leading to less heat production. Normally, when bodily functions are all working well, particularly the sweat glands, a person can handle extreme heat without a significant change in temperature; although, sometimes on very hot days, it may increase by half to one degree. The exact cause of heat stroke and its accompanying high fever is not well understood but is likely related to some effect on the brain’s heat regulation center. Heat exhaustion is also caused by prolonged exposure to heat, but it usually comes with a lower body temperature. Cold exposure, like freezing conditions, reduces all metabolic activities in the body. Temperature can be somewhat controlled through changes in diet, exercise levels, medications, and other factors.

Sense of Touch.—Before passing on to a discussion of the individual parts, a few words might well be said of the sense of touch, since that is general and resides largely in the skin, whose other [Pg 46] functions have just been described. It may be regarded as the form from which all the other special senses have developed, certain portions of the body having become more sensitive than others to certain vibrations, as the eye to those of light. The internal organs probably have little sense of touch.

Sense of Touch.—Before moving on to a discussion of the individual parts, it's worth mentioning the sense of touch, as it is general and mainly located in the skin, whose other [Pg 46] functions have just been described. It can be seen as the foundation from which all the other special senses have evolved, with specific areas of the body becoming more sensitive to certain vibrations, similar to how the eye responds to light. The internal organs likely have a minimal sense of touch.

Figs. 13, 14.—Meissner’s corpuscle from man; ×750.
(Böhm, Davidoff, and Huber.)

Figs. 13, 14.—Meissner’s corpuscle from humans; ×750.
(Böhm, Davidoff, and Huber.)

Touch is useful only within arm’s reach but there gives one a sense of space that sight does not give. It is practically determined by the touch corpuscles, which are found in the skin over almost the entire body, though they are more numerous in some places than in others, the distribution of the corpuscles determining the sensitiveness of the skin. These touch corpuscles are protoplasmic bodies containing nuclei, about which are entwined filaments from the cutaneous nerves. Where the corpuscles are absent the filaments of the cutaneous nerves themselves play an important part. The finger tips have a very delicate sense of touch and the tip of the tongue is the most sensitive part of the body. [Pg 47] Hence spaces in the mouth seem larger than elsewhere. By the transmission of sensations of touch to the brain the sensation is localized and the tactile sensation becomes a tactile perception.

Touch is only useful within arm's reach, but it provides a sense of space that sight doesn’t offer. It is mainly determined by the touch corpuscles, which are located in the skin across nearly the entire body, although they are more numerous in some areas than others. The way these corpuscles are distributed affects the sensitivity of the skin. These touch corpuscles are protoplasmic structures containing nuclei, around which filaments from the skin's nerves are wrapped. Where the corpuscles are absent, the nerve filaments themselves play a crucial role. The fingertips have a very fine sense of touch, and the tip of the tongue is the most sensitive part of the body. [Pg 47] This is why spaces in the mouth feel larger than in other areas. When touch sensations are transmitted to the brain, the sensation is localized, turning tactile sensation into tactile perception.

There are three main divisions of the sense of touch: 1. sensations of touch proper or tactile sensation; 2. sensations of temperature, and 3. sensations of pain. The temperature sense is the transmission by the skin of sensations not so much of a certain degree of heat or cold as of the difference between the temperature of an object and that of the skin. The longer an object is in contact with the skin, the less conscious the person is of it, not only because it becomes of the same temperature, but also because he becomes accustomed to it. There also seem to be in the skin, besides the touch corpuscles, two other terminal organs with separate nerve fibers, the one for detecting heat, the other cold; for there are places on the body where heat can be detected and cold cannot, and vice versa.

There are three main parts of the sense of touch: 1. sensations of touch itself or tactile sensation; 2. sensations of temperature; and 3. sensations of pain. The temperature sense involves the skin transmitting sensations that are less about a specific degree of heat or cold and more about the difference between an object's temperature and that of the skin. The longer an object is touching the skin, the less aware a person becomes of it, not just because it reaches the same temperature, but also because the person adapts to it. Additionally, it appears that the skin has, besides the touch receptors, two other types of nerve endings with separate fibers: one for detecting heat and another for cold; this is evident in areas of the body where heat can be sensed but cold cannot, and vice versa.

Sensations of pain may be merely an exaggeration of tactile sensation, as in too hard pressure or too great heat, but there seems to be also a sensation of pain in the skin. All organs are said to have common sensibility to pain and any exaggeration of this sensibility causes a sensation of pain. All the special senses require a certain amount of judgment in the interpretation of the sensations they convey.

Sensations of pain might just be an overreaction to touch, like too much pressure or extreme heat, but there also appears to be a specific pain sensation in the skin. It's said that all organs share a common sensitivity to pain, and any increase in this sensitivity leads to a feeling of pain. All the special senses need a bit of judgment to interpret the sensations they send.


CHAPTER III.
THE SKULL AND FACE.

The intelligence and all the special senses, except the sense of touch already spoken of, are gathered together compactly in the head, where they are carefully protected with bony tissue. Covering the brain is the skull or cranium, which is made up of eight bones, the frontal, the occipital, two parietal, two temporal, the sphenoid, and the ethmoid, while the bones of the face are fourteen in number, two nasal, two superior maxillary, two lachrymal, two malar, two palate, two inferior turbinated, the vomer, and the inferior maxillary. For the most part the bones are arranged in pairs, one on either side.

The intelligence and all the special senses, except for the sense of touch mentioned earlier, are compactly located in the head, where they’re well-protected by bony tissue. The skull, or cranium, covers the brain and is made up of eight bones: the frontal, occipital, two parietal, two temporal, sphenoid, and ethmoid. The bones of the face total fourteen: two nasal, two upper jaw (maxillary), two lacrimal, two cheek (malar), two palate, two lower turbinate, the vomer, and the lower jaw (inferior maxillary). Most of the bones are arranged in pairs, one on each side.

The Cranial Bones.—The cranium or skull is especially adapted for the protection of the brain and the bones are flat and closely fitted to its surface. They have two layers of bone, the outer and the inner tables, of which the outer is the thicker, and between these is a tissue filled with blood-vessels, the diploë. In the infant, whose brain has not yet attained its full size, opportunity must be left for growth and the skull therefore consists of a number of bones with interlocking notched edges, where growth takes place, but in the adult it forms one solid covering of bone.

The Cranial Bones.—The skull is specially designed to protect the brain, with the bones being flat and closely fitted to its surface. There are two layers of bone, the outer and the inner tables, with the outer being thicker. Between these layers is a tissue filled with blood vessels, called the diploë. In infants, whose brains haven't reached their full size yet, there's a need for growth, so the skull is made up of several bones with interlocking, notched edges where the growth occurs. However, in adults, it forms one solid layer of bone.

The line where the edges of two cranial bones come together is called a suture. The suture between the frontal bone and the forward edges of the two parietal bones is called the coronal suture, that between the two parietal bones at the vertex of the skull is known as the longitudinal or sagittal suture, and that between the occipital bone and the back edges of the parietal bones as the lambdoidal suture. [Pg 49]

The line where the edges of two skull bones meet is called a suture. The suture between the frontal bone and the front edges of the two parietal bones is called the coronal suture, the one between the two parietal bones at the top of the skull is known as the longitudinal or sagittal suture, and the one between the occipital bone and the back edges of the parietal bones is called the lambdoidal suture. [Pg 49]

Where the coronal and sagittal sutures meet is a membranous interval known as the anterior fontanelle, while the posterior fontanelle is at the juncture of the sagittal with the lambdoidal suture. These fontanelles—so called from the pulsations of the brain that can be seen in them—close after birth either by the extension of the surrounding bones or by the development in them of small bones known as Wormian bones, the posterior one closing within a few months, the anterior by the end of the second year. In rickets, however, the anterior fontanelle remains open a long time, sometimes into the fourth year.

Where the coronal and sagittal sutures meet is a soft spot called the anterior fontanelle, while the posterior fontanelle is located where the sagittal and lambdoidal sutures meet. These fontanelles—named for the pulsations of the brain that can be seen through them—close after birth either by the growth of the surrounding bones or by the formation of small bones known as Wormian bones. The posterior fontanelle usually closes within a few months, while the anterior fontanelle closes by the end of the second year. However, in cases of rickets, the anterior fontanelle can remain open for a long time, sometimes until the fourth year.

Fig. 15.—Cranium at birth, showing sutures and fontanelles.

Fig. 15.—Skull at birth, showing seams and soft spots.

The frontal bone, as its name implies, forms the fore part of the head or forehead. It joins the parietal bones above and the temporal bones on either side. At the lower edge are the supra-orbital arches, each with a supra-orbital notch or foramen on its inner margin for the passage of the supra-orbital vessels and nerve, the nerve most affected in neuralgia. Just above the arches on either side are the superciliary ridges, behind which, between the two tables of the skull, lie the frontal sinuses. On the inner surface the frontal sulcus for the longitudinal sinus runs along the median line.

The frontal bone, as its name suggests, forms the front part of the head or forehead. It connects the parietal bones above and the temporal bones on both sides. Along the lower edge are the supra-orbital arches, each with a supra-orbital notch or foramen on its inner edge for the passage of the supra-orbital vessels and nerve, which is most affected in cases of neuralgia. Just above the arches on either side are the superciliary ridges, behind which, between the two layers of the skull, the frontal sinuses are located. On the inner surface, the frontal sulcus for the longitudinal sinus runs along the center line.

The parietal bones are the side bones of the skull. They meet [Pg 50] each other in the sagittal suture at the median line above and join the frontal and occipital bones at either end, while below they touch upon the temporal bones, the temporal muscles being attached in part along their lower surface. These muscles are inserted into the coronoid process of the lower jaw, which they thus help to raise and to retract.

The parietal bones are the side bones of the skull. They meet [Pg 50] at the sagittal suture along the center line above and connect with the frontal and occipital bones at each end, while below they touch the temporal bones, where part of the temporal muscles are attached along their lower surface. These muscles are connected to the coronoid process of the lower jaw, helping to lift and pull it back.

Fig. 16.—Front view of the skull.
(After Sobotta.)

Fig. 16.—Front view of the skull.
(After Sobotta.)

The occipital bone is at the base of the skull and at birth consists of four pieces. In the lower, anterior part is the foramen magnum, an oval opening through which the spinal cord passes from the skull down into the spinal canal. Half way between the foramen and the top of the bone is the external occipital protuberance for the attachment of the ligamentum nuchæ which holds the head erect. The inner side of the bone is deeply concave and is divided by a cross-shaped grooved ridge into four fossæ, the internal occipital [Pg 51] protuberance being situated where the arms of the cross meet. The occipital lobes of the cerebrum lie in the two upper fossæ and the hemispheres of the cerebellum in the two lower ones. In the grooves upon the ridge are the sinuses which collect the blood from the brain.

The occipital bone is at the base of the skull and is made up of four pieces at birth. In the lower front part, there's the foramen magnum, an oval opening that allows the spinal cord to go from the skull into the spinal canal. Halfway between the foramen and the top of the bone is the external occipital protuberance for the attachment of the ligamentum nuchæ, which keeps the head upright. The inside of the bone is deeply concave and is divided by a cross-shaped grooved ridge into four depressions, with the internal occipital protuberance located at the intersection of the cross. The occipital lobes of the cerebrum are found in the two upper depressions, and the hemispheres of the cerebellum are in the two lower ones. The grooves on the ridge contain the sinuses that collect blood from the brain.

The occipital and frontal muscles, united by a thin aponeurosis, cover the whole upper cranium and are known as the occipito-frontalis muscle. At the back this is attached to the occipital bone, while in front it interlaces with various face muscles. It is a powerful muscle and raises the brows, wrinkles the forehead, and draws the scalp forward. Long hair grows on the skin over it as a further protection against blows upon the skull and sudden variations in temperature.

The occipital and frontal muscles, linked by a thin connective tissue, cover the entire upper skull and are referred to as the occipito-frontalis muscle. At the back, it is attached to the occipital bone, while in the front, it intertwines with several facial muscles. It's a strong muscle that raises the eyebrows, wrinkles the forehead, and pulls the scalp forward. Long hair grows on the skin over it, providing additional protection against impacts to the skull and sudden changes in temperature.

The temporal bones—said to be so named because the hair over them is the first to turn with age—are situated at the sides and base of the skull and are in three portions: the squamous or scale-like, the mastoid or nipple-like, and the petrous or stony portion. The squamous is the upper portion and has projecting from its lower part the long arched zygomatic process, which articulates with the malar bone of the face and from which arises the masseter muscle, one of the chief muscles of mastication, which has its insertion in the ramus and angle of the lower jaw. Just above the zygomatic process the temporal muscle has its origin in part, while below is the glenoid fossa for articulation with the condyle of the lower jaw, the posterior portion of the fossa being occupied by part of the parotid gland.

The temporal bones—named because the hair over them is the first to gray with age—are located at the sides and base of the skull and are divided into three parts: the squamous or scale-like, the mastoid or nipple-like, and the petrous or stony part. The squamous is the upper part and has the long, arched zygomatic process extending from its lower section, which connects with the malar bone of the face and gives rise to the masseter muscle, one of the main muscles used for chewing, which attaches at the ramus and angle of the lower jaw. Just above the zygomatic process, the temporal muscle partially originates, while below is the glenoid fossa for connecting with the condyle of the lower jaw, with the back part of the fossa containing part of the parotid gland.

The rough mastoid portion of the temporal bone is toward the back and affords attachment to various muscles, of which the most important are the occipito-frontalis and the sterno-cleido-mastoid. Within it are the mastoid cells, which communicate with the inner ear and are lined with mucous membrane continuous with that of the tympanum. They probably have something to do with the hearing. In children they often become [Pg 52] the seat of inflammation (mastoid abscess) in infectious diseases and the mastoid bone has to be cut to let out pus that has collected. As the lateral sinus is directly behind the mastoid bone, there is very great danger of going through into the sinus and causing a fatal hemorrhage.

The rough mastoid part of the temporal bone is located at the back and serves as an attachment point for various muscles, with the most important being the occipito-frontalis and the sterno-cleido-mastoid. Inside are the mastoid cells, which connect to the inner ear and are lined with a mucous membrane that is continuous with that of the tympanum. They likely play a role in hearing. In children, these cells often become infected (mastoid abscess) during illnesses, and the mastoid bone may need to be cut to drain the pus that has accumulated. Since the lateral sinus is directly behind the mastoid bone, there's a significant risk of accidentally penetrating it and causing severe bleeding.

Fig. 17.—Side view of the skull.
(After Sobotta.)

Fig. 17.—Side view of the skull.
(After Sobotta.)

The petrous portion, which contains the organ of hearing, is between and somewhat behind the other two portions, at the lower edge of the temporal bone, wedged between the sphenoid and the occipital bones. On its outer surface is the external auditory meatus, and from below projects a long sharp spine called the styloid process, to which several minor muscles are attached. In the same angle between the petrous and squamous portions lies the bony Eustachian tube.

The petrous portion, which holds the hearing organ, is located between and slightly behind the other two portions at the lower edge of the temporal bone, wedged between the sphenoid and occipital bones. The external auditory meatus is on its outer surface, and from below, a long sharp spine called the styloid process protrudes, to which several minor muscles are attached. In the same angle between the petrous and squamous portions is the bony Eustachian tube.

The sphenoid or wedge bone, so called because in the process of development it serves as a wedge, lies at the base of the cranium, forming as it were the anterior part of the floor of the [Pg 53] cavity containing the brain. It is a large, bat-shaped bone and articulates with all the cranial and many of the facial bones, binding them all together. It has a body, two large wings, and two lesser wings and, appears on the outside of the skull between the frontal and the temporal bones behind the zygomatic process. In the adult the body of the sphenoid is hollowed out into the sphenoid sinuses, in which pus sometimes forms.

The sphenoid or wedge bone, named for its wedge shape during development, is located at the base of the skull, making up the front part of the floor of the [Pg 53] cavity that holds the brain. It’s a large, bat-shaped bone that connects with all the cranial bones and many facial bones, holding them all together. It has a body, two large wings, and two smaller wings, and it can be seen on the outside of the skull between the frontal and temporal bones, behind the zygomatic process. In adults, the body of the sphenoid is hollowed out into the sphenoid sinuses, which can sometimes fill with pus.

The Ethmoid Bone.—In front of and below the sphenoid and extending forward to the frontal bone is the ethmoid, the last of the cranial bones. It consists of a horizontal cribriform or sieve-like plate, from either side of which depend lateral masses of ethmoid cells. To the inner side of these masses are attached the thin curved turbinated bones, superior and middle, while between them is a vertical plate that forms the bony septum of the nose. Rising from the upper surface of the cribriform plate is another vertical plate, the crista galli, with the olfactory grooves on either side for the reception of the olfactory bulbs, filaments of the olfactory nerve passing down through the perforations of the cribriform plate to the nose. For the brain, which fills almost the entire cavity of the cranium, is supported by the sphenoid and ethmoid bones internally, as it is protected externally by the other cranial bones.

The Ethmoid Bone.—Located in front of and below the sphenoid and extending forward to the frontal bone is the ethmoid, the last of the cranial bones. It features a horizontal cribriform plate, which is sieve-like, with lateral masses of ethmoid cells hanging down from either side. Attached to the inner side of these masses are the thin, curved turbinated bones, superior and middle, while a vertical plate between them forms the bony septum of the nose. Rising from the upper surface of the cribriform plate is another vertical plate, the crista galli, with olfactory grooves on either side to hold the olfactory bulbs, as filaments of the olfactory nerve pass through the perforations of the cribriform plate to the nose. The brain, which occupies almost the entire cavity of the cranium, is supported internally by the sphenoid and ethmoid bones and is protected externally by the other cranial bones.

Ossification of Sutures.—If premature ossification of all the sutures occurs, idiocy results, while in cephalocele there is a gap in the ossifying of the bones so that the membranes or brain protrude. In rickets the forehead is high and square and the face bones poorly developed, so that the head looks larger than it really is. In Paget’s disease the bones enlarge and soften. This affects the head but not the face and often the first thing noticed is that the hat is too small. Craniotabes is thinning of the bone in places, the bone becoming like parchment and being easily bent. It is generally caused by pressure of the pillow or the nurse’s arm.

Ossification of Sutures.—If all the sutures fuse too early, it leads to idiocy. In cases of cephalocele, there’s a gap in the bone development that allows membranes or brain tissue to stick out. With rickets, the forehead appears high and squared off, and the facial bones are underdeveloped, making the head look larger than it actually is. In Paget’s disease, the bones grow larger and become softer. This condition affects the head but not the face, and often the first sign is that a hat feels too tight. Craniotabes refers to areas where the bone thins out, making it feel like parchment and easy to bend. It’s usually caused by pressure from a pillow or a nurse’s arm.

Bones of the Face.—The facial bones serve to form the various [Pg 54] features of the face, which after all are merely organs of special sense. Many delicate muscles control the facial expression which, consciously or unconsciously, reflects the character of their owner.

Bones of the Face.—The facial bones shape the different [Pg 54] features of the face, which are essentially organs of special sense. Numerous delicate muscles manage facial expressions that, consciously or not, reveal the personality of their owner.

Surgically the most important of the facial bones are the two superior maxillary bones, because of the number of diseases to which they are liable. They meet in front, together forming the upper jaw, and with the malar bone help form the lower part of the orbit of the eye. They are cuboid in shape and are hollowed out into a pyramidal cavity called the antrum of Highmore, which opens by a small orifice into the middle nasal meatus and which sometimes becomes infected and has to be tapped. The nasal process for articulation with the frontal and nasal bones has, at its lower edge, a crest for the inferior turbinated bone, and close beside this on the inside, extending down from the upper edge, is a deep groove which, with the lachrymal and inferior turbinated bones, helps to form the lachrymal canal for the nasal tear duct. The bones give attachment to many small muscles, connected for the most part with the nose and mouth, of which the masseter is the only important one.

Surgically, the most important of the facial bones are the two superior maxillary bones, due to the various diseases they can be prone to. They meet at the front, together forming the upper jaw, and with the cheekbone, help create the lower part of the eye socket. They are cube-shaped and have a pyramidal cavity called the antrum of Highmore, which opens through a small hole into the middle nasal meatus and can sometimes get infected, requiring drainage. The nasal process connects with the frontal and nasal bones, featuring a ridge at its lower edge for the inferior turbinated bone. Right next to this on the inner side, there is a deep groove that, along with the lachrymal and inferior turbinated bones, forms the lachrymal canal for the nasal tear duct. These bones provide attachment for many small muscles, mostly associated with the nose and mouth, with the masseter being the only significant one.

The two malar or cheek bones are small quadrangular bones, which form the prominences of the cheeks and help form the orbits of the eyes. Projecting backward from each is a zygomatic process for articulation with the zygomatic process of the temporal bone, while a maxillary process extends downward for articulation with the superior maxillary. Here again the most important muscle attached is the masseter. If the malar bone is crushed great deformity results.

The two malar or cheek bones are small rectangular bones that create the shape of the cheeks and contribute to the eye sockets. Each bone has a zygomatic process that connects to the zygomatic process of the temporal bone, while a maxillary process extends downward to connect with the upper jaw. The main muscle attached here is the masseter. If the cheekbone is crushed, it can lead to significant deformity.

The lachrymal bones are two small bones, about the size and shape of a finger-nail, situated at the front of the inner wall of the orbit. At the external edge is a groove which lodges the lachrymal sac above and forms part of the lachrymal canal below.

The lachrymal bones are two tiny bones, roughly the size and shape of a fingernail, located at the front of the inner wall of the eye socket. At the outer edge, there’s a groove that holds the lachrymal sac above and makes up part of the lachrymal canal below.

The two palate bones are at the back of the nasal fossæ and help to form the floor of the nose, the roof of the mouth, and the orbit. Each [Pg 55] has a vertical and a horizontal plate, and it is these last that by their juncture form the hard palate. Oftentimes in cases of hare-lip cleft palate also occurs, the result of incomplete development. To remedy the consequent opening in the roof of the mouth, which makes articulation difficult, operation is generally resorted to, though sometimes a plate is fitted over the opening by a dentist.

The two palate bones are located at the back of the nasal cavities and contribute to forming the floor of the nose, the roof of the mouth, and the eye socket. Each [Pg 55] has a vertical and a horizontal plate, and it's these last plates that, when they connect, create the hard palate. Often, in cases of cleft lip, cleft palate also occurs due to incomplete development. To fix the resulting opening in the roof of the mouth, which makes speaking hard, surgery is usually performed, though sometimes a dentist will make a plate to cover the opening.

The nasal bones are two small oblong bones which articulate with the frontal and superior maxillary bones and with each other. They form the bridge of the nose, the rest of the nose being wholly of cartilage, except for the vomer, a bone shaped like a plough-share, which forms part of the nasal septum, articulating along its anterior edge with the ethmoid and the triangular cartilage.

The nasal bones are two small, elongated bones that connect with the frontal and upper jaw bones, as well as with each other. They create the bridge of the nose, while the rest of the nose is entirely made of cartilage, except for the vomer, a bone shaped like a plow, which is part of the nasal septum and connects at its front edge with the ethmoid and the triangular cartilage.

The two inferior turbinated bones lie along the outer walls of the nasal fossæ. They are thin scroll-like bones covered with mucous membrane and serve to heat the air as it passes in. Sometimes when one has a cold, the membrane and the bone too swell up and close the nares. Loss of the sense of smell in a bad cold may be due to such swelling and the consequent impeding of the entrance of odoriferous particles—a condition that would likewise interfere with the sense of taste. Part of the bone is sometimes removed, to enlarge the passage, enough being left to warm the air.

The two inferior turbinated bones are located along the outer walls of the nasal passages. They are thin, scroll-like bones covered with a mucous membrane that helps warm the air as it enters. When someone has a cold, the membrane and the bones can swell, blocking the nostrils. Losing the sense of smell during a bad cold may be due to this swelling, which can also prevent odor particles from entering—this condition can also affect the sense of taste. Sometimes, part of the bone is removed to widen the passage, leaving enough to still warm the air.

Lastly, there is the inferior maxillary bone or lower jaw. This has a horseshoe-shaped body and two rami, one at either end. Each ramus has a pointed process in front called the coronoid process, into which is inserted the temporal muscle. At the back, and separated from the coronoid process by the sigmoid notch, is the condyle, which articulates with the glenoid fossa on the temporal bone. The rami also give attachment to the masseter muscle at its point of insertion. In adult age the ramus is almost vertical but in old age the portion of the jaw hollowed out into alveoli for the teeth becomes absorbed and [Pg 56] the angle of the jaw becomes very obtuse. On the inner side of the jaw near the middle on either side is the fossa for the sublingual gland, while the submaxillary gland lies in a fossa farther back on either side.

Lastly, there is the inferior maxillary bone or lower jaw. This has a horseshoe-shaped body and two rami, one at each end. Each ramus has a pointed process in front called the coronoid process, where the temporal muscle attaches. At the back, separated from the coronoid process by the sigmoid notch, is the condyle, which connects with the glenoid fossa on the temporal bone. The rami also provide attachment for the masseter muscle at its insertion point. In adults, the ramus is nearly vertical, but in older age, the area of the jaw hollowed out for the teeth gets absorbed and the angle of the jaw becomes very obtuse. On the inner side of the jaw, near the center on either side, is the fossa for the sublingual gland, while the submaxillary gland is located in a fossa further back on either side. [Pg 56]

Sometimes the lower jaw is dislocated and when once this has occurred it is liable to occur again, the ligaments becoming stretched.

Sometimes the lower jaw gets dislocated, and once that happens, it can happen again since the ligaments become stretched.


CHAPTER IV.
The special sense organs.

The Nose.—The nose, the organ of the sense of smell, is composed of a framework of bones and cartilages, the bridge being formed by the two nasal bones, and the septum by the vomer and the triangular cartilage. It consists of two parts, the external nose and the internal or nasal fossæ, which open to the face by the anterior nares or nostrils and into the pharynx by the posterior nares. Externally it is covered with skin, internally with ciliated mucous membrane. The fossæ have the inferior turbinated bones along their outer walls and are divided into three parts known as the superior, the middle, and the inferior meatus, the middle one connecting with the antrum of Highmore, while into the inferior meatus the lachrymal canal empties. There are many small muscles of which little use is [Pg 58] made, although in forced respiration, as in pneumonia, where every aid to breathing is called into play, even the alæ nasi or nostrils are made to exert what muscular power they possess in order to supply more air.

The Nose.—The nose, the organ responsible for the sense of smell, is made up of a structure of bones and cartilage, with the bridge formed by the two nasal bones and the septum created by the vomer and the triangular cartilage. It has two parts, the external nose and the internal or nasal fossæ, which connect to the face through the front openings known as nostrils and to the pharynx through the back openings. The outside is covered in skin, while the inside has a ciliated mucous membrane. The fossæ have the lower turbinated bones along their outer walls and are divided into three sections known as the superior, the middle, and the inferior meatus, with the middle section linking to the antrum of Highmore, while the lachrymal canal empties into the inferior meatus. There are many small muscles that aren't used much, but during forced breathing, like in pneumonia, when every effort to breathe is needed, even the alæ nasi or nostrils will use whatever muscle power they have to take in more air.

Fig. 18.—The nasal cavity.
(After Sobotta.)

Fig. 18.—Nasal cavity.
(After Sobotta.)

Not only is most of the air breathed in through the nose and warmed in its passage through, but the nose is the organ of smell and by means of the peculiar property of its nerves protects the lungs against deleterious gases and helps the taste discriminate. The olfactory or first cranial nerves, after emerging from the brain, lie on the under surface of the frontal lobe and rest on the ethmoid bone in what is known as the olfactory tract. Each nerve ends in a bulb-like termination called an olfactory bulb, which rests on the cribriform plate and sends little terminal fibers down through to be distributed to the nasal cavities, especially to the upper half of the septum of the nose, the roof of the nose, and the anterior and middle turbinated bones. For in the mucous membrane of the upper nasal cavity are specially modified epithelial cells called olfactory cells, which play an important part in the conduction of smell. Hence when one wishes to smell anything especially well he sniffs it up.

Not only is most of the air taken in through the nose and warmed as it passes through, but the nose also serves as the organ of smell and, due to the unique properties of its nerves, protects the lungs from harmful gases and aids in distinguishing tastes. The olfactory or first cranial nerves, after they emerge from the brain, are positioned on the underside of the frontal lobe and rest on the ethmoid bone in an area known as the olfactory tract. Each nerve ends in a bulb-like structure called an olfactory bulb, which sits on the cribriform plate and sends small terminal fibers down to be spread throughout the nasal cavities, especially to the upper part of the nasal septum, the roof of the nose, and the anterior and middle turbinates. Within the mucous membrane of the upper nasal cavity are specially modified epithelial cells called olfactory cells, which play a crucial role in the sense of smell. Therefore, when someone wants to smell something really well, they sniff it in.

Probably the sensation of smell is caused by odoriferous particles in the atmosphere being breathed into the nose, where they affect the olfactory cells, which transmit the impulses to the olfactory nerve and so to the brain. Whereas a certain amount of moisture in the nasal cavity seems to be essential for accuracy of smell, the presence of too much or too little interferes with it. The mucous membrane has a certain power also of distinguishing different smells at the same time, though this power varies greatly in different people, one smell often wholly overpowering all others.

Probably the sensation of smell is caused by fragrant particles in the air being inhaled into the nose, where they impact the olfactory cells. These cells send signals to the olfactory nerve and then to the brain. While some moisture in the nasal cavity appears to be necessary for accurate smelling, too much or too little can disrupt it. The mucous membrane also has a certain ability to recognize different smells at the same time, although this ability varies significantly among individuals, with one scent often completely dominating all the others.

The cartilage below the bridge of the nose is sometimes attacked in syphilis and cancer, and lupus often begins on the nose. Deviation of the septum may occlude all air from one side of the nose, an effect also produced by polypi, generally of the turbinated [Pg 59] bone. Either condition is easily remedied. Nosebleed, though generally unimportant, may be serious in adults.

The cartilage under the bridge of the nose can sometimes be affected by syphilis and cancer, and lupus often starts on the nose. Deviation of the septum can block airflow from one side of the nose, a problem also caused by polypi, usually from the turbinated [Pg 59] bone. Both conditions are easy to fix. Nosebleed, while usually not serious, can be significant in adults.

The Mouth.—The mouth is of great importance as an entrance for fresh air to the lungs when the nasal passages are for any reason impeded and as the resonant chamber from which proceeds the voice, man’s chief means of communication with his fellows. Its chief value may be said, however, to reside in the fact that it is the vestibule of the alimentary canal. It is an ovoid cavity lined with mucous membrane and is bounded in front by the lips, at the sides by the cheeks, below by the floor and tongue, and above by the hard palate anteriorly and by the soft palate posteriorly, the uvula depending from the latter like a curtain between the mouth and the pharynx. Shape is given to the mouth by the bones of the upper and lower jaw and its size is altered by the lowering and raising of the latter, which is quite freely movable.

The Mouth.—The mouth is very important as an entrance for fresh air to the lungs when the nasal passages are blocked for any reason and as the resonant chamber that produces the voice, which is humanity’s primary way of communicating. Its main value lies in the fact that it serves as the entrance to the digestive system. It is an oval-shaped cavity lined with mucous membrane and is bordered in front by the lips, on the sides by the cheeks, below by the floor and tongue, and above by the hard palate in the front and the soft palate in the back, with the uvula hanging from the latter like a curtain between the mouth and the pharynx. The shape of the mouth is defined by the bones of the upper and lower jaw, and its size can change as the lower jaw moves up and down, which it does quite freely.

Fig. 19.—The hyoid bone. (Toldt.)

Fig. 19.—The hyoid bone. (Toldt.)

At the back of the mouth, at the entrance to the pharynx, are the anterior and posterior pillars of the fauces, which contain muscular tissue, and between which on either side are thick masses of lymphoid tissue, the tonsils. The floor of the mouth is formed largely by the tongue, which completely fills the space within the [Pg 60] lower teeth. Its base or root is directed backward and downward and is attached by muscles to the hyoid bone and the lower jaw, the hyoid bone being a horseshoe-shaped bone lying just below and as it were within the inferior maxillary. The base of the tongue is attached also to the epiglottis and at the sides to the soft palate by the anterior pillars. Except at its base and the posterior part of its under surface the tongue is free, but a fold of mucous membrane, the frenum, holds it somewhat in front. Thus it possesses great versatility of motion and serves as an auxiliary in articulation, mastication, and deglutition.

At the back of the mouth, at the opening to the throat, are the anterior and posterior pillars of the fauces, which are made of muscle tissue, and between them on each side are thick clusters of lymphoid tissue known as tonsils. The floor of the mouth is mostly formed by the tongue, which fills the space inside the [Pg 60] lower teeth. Its base or root points backward and downward and is connected by muscles to the hyoid bone and the lower jaw, with the hyoid bone being a horseshoe-shaped bone located just below and somewhat within the lower jaw. The base of the tongue is also connected to the epiglottis and at the sides to the soft palate by the anterior pillars. Except for its base and the back part of its underside, the tongue is free, but a fold of mucous membrane called the frenum keeps it somewhat in place at the front. This allows it to have a lot of movement and helps with speaking, chewing, and swallowing.

The Teeth.—Securely embedded in either jaw are the teeth, nature’s instrument for the first preparation of the food for digestion through tearing and grinding. The incisors, which are in front, have wide sharp edges for cutting the food. Next come the canine teeth with a sharp point for tearing it, while at the back are the molars with a broad flat top for grinding.

The Teeth.—Securely embedded in either jaw are the teeth, nature’s tool for the initial preparation of food for digestion through tearing and grinding. The incisors, which are in front, have wide sharp edges for cutting food. Next are the canine teeth with a sharp point for tearing, while at the back are the molars with a broad flat top for grinding.

There are two sets of teeth: 1. the temporary or milk teeth, twenty in number—four incisors, two canines, and four molars in each jaw—which appear at from six months to two years, and 2. the permanent teeth, thirty-two in number—four incisors, two canines, known as eye teeth in the upper jaw and as stomach teeth in the lower jaw, four bicuspids, so called because they have two cusps where the molars have four or five, and six molars in each jaw—which come from the sixth to the twenty-first years. The first to appear are the two lower middle incisors, which come at the age of six months. The last to appear are the wisdom teeth, the farthest back of the molars, which come at the age of twenty-one years or thereabouts.

There are two sets of teeth: 1. the temporary or milk teeth, which total twenty—four incisors, two canines, and four molars in each jaw—that appear between six months and two years, and 2. the permanent teeth, which total thirty-two—four incisors, two canines, referred to as eye teeth in the upper jaw and stomach teeth in the lower jaw, four bicuspids, named for having two cusps compared to the four or five of molars, and six molars in each jaw—that emerge between the ages of six and twenty-one. The first to come in are the two lower middle incisors, arriving at around six months. The last to come in are the wisdom teeth, the ones at the back of the molars, which typically appear at around twenty-one years old.

Each tooth consists of a crown or body above the gum, a neck, and a fang or root within the gum. The body is of dentine or ivory with a thin crust of enamel and contains the pulp, a vascular connective tissue containing many nerves. Beginning at the neck and covering the fang is a layer of cement or true bone. [Pg 61]

Each tooth has a crown or body above the gum, a neck, and a fang or root below the gum. The body is made of dentine or ivory with a thin layer of enamel and contains the pulp, a connective tissue with lots of nerves. Starting at the neck and wrapping around the fang is a layer of cement or true bone. [Pg 61]

The Sense of Taste.—The sense of taste lies chiefly in the taste buds as they are called which are filled with gustatory cells and are found in the papillæ of the tongue, principally in the circumvallate papillæ at the back of the tongue, which are few in number and arranged in a V-shape. There is also a certain power of taste in the tip and sides of the tongue but little in the upper surface or dorsum. Only five special tastes can be distinguished: bitter, sweet, acid, sour, and salt, but sometimes more than one can be distinguished at a time, as bitter and sweet. Every one can distinguish between different tastes but the power varies in different people and with different conditions. Certain tastes seem to be better distinguished in certain places, as sweet at the tip and bitter at the back of the tongue. Moreover, the sense of taste is very dependent upon the sense of smell, especially in the case of aromatic and savory substances, which one really does not taste but smell. If one held his nose and closed his eyes he would not know from the taste whether he was eating onion or apple. This leads to the habit of pinching the nose when taking nauseous medicines.

The Sense of Taste.—The sense of taste mainly comes from the taste buds, which contain gustatory cells and are located in the papillæ of the tongue, especially in the circumvallate papillæ at the back of the tongue. These are few in number and arranged in a V-shape. There is also some ability to taste at the tip and sides of the tongue, but not much on the upper surface or dorsum. Only five basic tastes can be identified: bitter, sweet, acidic, sour, and salty, but sometimes multiple tastes can be recognized at once, like bitter and sweet. Everyone can tell different tastes apart, but this ability varies among individuals and under different conditions. Certain tastes seem to be easier to identify in specific areas, such as sweetness at the tip and bitterness at the back of the tongue. Additionally, the sense of taste heavily relies on the sense of smell, especially when it comes to aromatic and flavorful foods, which are often more about smell than taste. If someone holds their nose and closes their eyes, they wouldn't be able to tell if they were eating onion or apple just by the taste. This is why people often pinch their noses when taking unpleasant medicines.

To be tasted a substance must be in solution. Friction against the tongue, lips or cheek increase the sense of taste. A temperature of 100° Fahrenheit favors taste, while both great heat and great cold impair it.

To be tasted, a substance needs to be in solution. Rubbing against the tongue, lips, or cheek enhances the sense of taste. A temperature of 100° Fahrenheit is ideal for tasting, while extreme heat or extreme cold can dull it.

There are probably at least two nerves of taste, the lingual branch of the trifacial or fifth cranial and the gustatory branch of the glosso-pharyngeal.

There are likely at least two nerves that sense taste: the lingual branch of the trigeminal nerve (fifth cranial nerve) and the gustatory branch of the glossopharyngeal nerve.

Along with the sense of taste there are other senses in the mouth which play an important part, such as pressure and the sense of heat and cold, and it is often hard to distinguish them from the pure sensation of taste, which indeed is always accompanied by them.

Along with the sense of taste, there are other sensations in the mouth that play a crucial role, like pressure and the sensation of heat and cold, and it can often be difficult to separate them from the actual taste experience, which is always influenced by these sensations.

Salivary Glands.—On either side of the mouth are three racemose glands for the secretion of the saliva, which serves to soften and lubricate the food and partially to digest starches by means of its [Pg 62] ferment, ptyalin. The parotid gland is the largest and is below and in front of the ear, opening by Stensen’s duct. The submaxillary gland is below the jaw toward the back on either side and its duct is Wharton’s duct. The sublingual gland lies beneath the mucous membrane of the floor of the mouth and opens by eight to twenty tiny ducts beside the frenum, the ducts of Rivinus. The activity of the glands depends upon the blood supply; the more blood the greater their activity.

Salivary Glands.—On each side of the mouth, there are three racemose glands that produce saliva, which helps to soften and lubricate food and partially break down starches with its enzyme, ptyalin. The parotid gland is the largest and is located below and in front of the ear, opening through Stensen’s duct. The submaxillary gland is situated below the jaw toward the back on either side, and its duct is Wharton’s duct. The sublingual gland is located beneath the mucous membrane of the floor of the mouth and opens through eight to twenty small ducts next to the frenum, known as the ducts of Rivinus. The activity of these glands is influenced by the blood supply; the more blood they receive, the more active they are.

Fig. 20.—Dissection of the side of the face, showing the salivary glands: a, Sublingual gland; b, submaxillary gland, with its duct opening on the floor of the mouth beneath the tongue at d; c, parotid gland and its duct, which opens on the inner side of the cheek. (After Yeo.)

Fig. 20.—Dissection of the side of the face, showing the salivary glands: a, Sublingual gland; b, submaxillary gland, with its duct opening on the floor of the mouth beneath the tongue at d; c, parotid gland and its duct, which opens on the inner side of the cheek. (After Yeo.)

The Tonsils.—The tonsils vary in size and in tonsillitis swell and may even meet in the median line. They are frequently removed. When they are enlarged one often gets a third tonsil or adenoids, a lymphoid growth at the back of the pharynx which causes mouth-breathing by day and snoring by night. A child with adenoids is starved for air and what air is breathed in is not warmed. The growth should be removed.

The Tonsils.—Tonsils come in different sizes and can swell up during tonsillitis, sometimes even touching in the middle. They are often removed. When they get larger, you might also have a third tonsil or adenoids, which is a lymphoid growth at the back of the throat that can cause mouth-breathing during the day and snoring at night. A child with adenoids struggles to get enough air, and the air they do breathe isn’t warmed. This growth should be removed.

A short frenum produces tongue-tie, which may be remedied by snipping. Cancer of the tongue is fairly common and necessitates a radical operation. In mumps the parotid glands are inflamed and enlarged. [Pg 63]

A short frenum causes tongue-tie, which can be fixed by snipping. Tongue cancer is relatively common and requires a major operation. In mumps, the parotid glands become inflamed and swollen. [Pg 63]

The Ear.—The special organ of hearing is the ear, to which there are three parts, the external, the middle, and the internal ear.

The Ear.—The special organ for hearing is the ear, which has three parts: the outer ear, the middle ear, and the inner ear.

The external ear consists of the pinna or expanded cartilaginous portion, for the concentration and direction of sound waves, and the external auditory canal, partly cartilage, partly bone, which is directed forward, inward, and downward and conveys sound to the middle ear.

The external ear is made up of the pinna, which is the larger, cartilaginous part that helps capture and direct sound waves, and the external auditory canal, which is made of both cartilage and bone. This canal goes forward, inward, and downward, transmitting sound to the middle ear.

Fig. 21.—The small bones of the ear; external view (enlarged).
(After Gray.)

Fig. 21.—The tiny bones of the ear; outside view (enlarged).
(After Gray.)

The middle ear or tympanum is an irregular cavity in the petrous portion of the temporal bone. Its outer wall is formed by the membrana tympani or drum, an oval translucent membrane placed obliquely at the bottom of the external auditory canal. The middle ear communicates with the inner ear through the fenestra ovalis or oval window and contains the ossicles, the malleus or hammer, the incus or anvil, and the stapes or stirrup, which are arranged in a movable chain from the drum to the oval window. The malleus, which is connected with the membrana tympani, articulates by its head with the body of the incus, while the stapes articulates with the incus by its head and is connected by its base with the margin of the oval window. Connection is made between the middle ear and the pharynx and the pressure of the air upon the drum made equal on either side by means of the Eustachian tubes. These tubes are about an inch and a half long, have cilia, and [Pg 64] convey wax and other matter from the ear to the pharynx. Occasionally in a cold or for some other reason they become stopped up and trouble results in the middle ear. Some of the mastoid cells also connect with the middle ear and may become infected, causing mastoid disease.

The middle ear or tympanum is an uneven space in the hard part of the temporal bone. Its outer wall is made up of the membrana tympani or drum, a translucent oval membrane positioned at an angle at the end of the external auditory canal. The middle ear connects to the inner ear through the fenestra ovalis or oval window and contains the ossicles, the malleus or hammer, the incus or anvil, and the stapes or stirrup, which are linked in a movable chain from the drum to the oval window. The malleus, which is attached to the membrana tympani, connects at its head with the body of the incus, while the stapes connects with the incus at its head and is linked at its base to the edge of the oval window. There is a connection between the middle ear and the pharynx, equalizing the air pressure on either side of the drum through the Eustachian tubes. These tubes are about an inch and a half long, have tiny hair-like structures, and [Pg 64] transport wax and other debris from the ear to the pharynx. Sometimes, during a cold or for other reasons, they can get blocked, leading to issues in the middle ear. Some of the mastoid cells also connect with the middle ear and can become infected, resulting in mastoid disease.

Fig. 22.—Interior view of left bony labyrinth after removal of the superior and external walls: 1, 2, 3, the superior, posterior, and external or horizontal semicircular canals; 4, fovea hemi-elliptica; 5, fovea hemispherica; 6, common opening of the superior and posterior semicircular canals; 7, opening of the aqueduct of the vestibule; 8, opening of the aqueduct of the cochlea; 9, the scala vestibuli; 10, scala tympani; the lamina spiralis separating 9 and 10. (From Quain, after Sömmerring.)

Fig. 22.—Interior view of the left bony labyrinth after the removal of the superior and outer walls: 1, 2, 3, the superior, posterior, and external (horizontal) semicircular canals; 4, fovea hemi-elliptica; 5, fovea hemispherica; 6, shared opening of the superior and posterior semicircular canals; 7, opening of the vestibular aqueduct; 8, opening of the cochlear aqueduct; 9, the scala vestibuli; 10, scala tympani; the spiraled lamina separating 9 and 10. (From Quain, after Sömmerring.)

The internal ear consists of various chambers hollowed out in the petrous portion of the temporal bone. There is an osseous labyrinth, consisting of a central cavity known as the vestibule, three semicircular canals, and the cochlea and within the osseous labyrinth, surrounded by perilymph, is the membranous labyrinth, of like form, filled with the endolymph. Communication exists externally with the middle ear by the round and oval windows and internally with the internal auditory canal, through which passes the eighth cranial or auditory nerve, the special nerve of hearing, which is distributed to the inner ear only. When the auditory nerve enters the ear through this internal auditory meatus it divides into two branches, [Pg 65] of which one goes to the vestibule and the other to the organ of Corti, a group of specially modified epithelial cells in the cochlea of the membranous labyrinth, which is very important in transmitting the impulses to the brain. The nerve also breaks up into very small branches and is distributed practically throughout the wall of the labyrinth.

The inner ear is made up of several chambers carved out in the hard part of the temporal bone. It includes an bony labyrinth, which has a central space called the vestibule, three semicircular canals, and the cochlea. Inside the bony labyrinth, surrounded by perilymph, is the membranous labyrinth, which has a similar shape and is filled with endolymph. There is communication with the middle ear through the round and oval windows and internally with the internal auditory canal, which is where the eighth cranial or auditory nerve, the specific nerve for hearing, enters. This nerve is only distributed to the inner ear. When the auditory nerve comes into the ear through this internal auditory canal, it splits into two branches, [Pg 65] one that goes to the vestibule and the other that goes to the organ of Corti, a group of specially modified epithelial cells in the cochlea of the membranous labyrinth that plays a crucial role in transmitting signals to the brain. The nerve also breaks into very small branches and spreads throughout the walls of the labyrinth.

The sensation of hearing is the result of impulses transmitted to the auditory nerve and so conveyed to the auditory center in the brain. It is caused by sound waves which travel through the air from their point of origin and enter the external ear. This collects and selects the waves of sound and helps one to a certain extent to determine the direction from which the sound comes. As they pass through the external meatus the sound waves are collected into a comparatively small area for transmission to the middle ear, where, by means of the drum, they set in vibration the chain of ossicles. Through these the vibrations are in turn transmitted to the oval window, being intensified in the process. Here again they are taken up by the perilymph, from which they pass through the wall of the membranous labyrinth to the endolymph, affecting the epithelial lining of the labyrinth in such a way that the impulses are transmitted to the auditory nerve, more particularly in the vestibule, from which the vibrations enter the cochlea. They also affect the cells of the organ of Corti in like manner as they pass from the perilymph to the endolymph. The membrane that covers the fenestra rotunda or round window relaxes and expands as the vibrations strike it, thus serving to eliminate the shock of impact.

The sensation of hearing comes from impulses sent to the auditory nerve and then transferred to the auditory center in the brain. It's triggered by sound waves that travel through the air from their source and enter the outer ear. This part collects and filters the sound waves, helping to some extent to figure out where the sound is coming from. As the sound waves pass through the external ear canal, they are gathered into a smaller area for transmission to the middle ear, where the eardrum vibrates and moves a chain of tiny bones. These vibrations are then passed to the oval window, getting stronger along the way. At this point, they enter the perilymph, travel through the wall of the membranous labyrinth to the endolymph, and affect the epithelial lining of the labyrinth so that the impulses get sent to the auditory nerve, particularly in the vestibule, where the vibrations then enter the cochlea. They also influence the cells of the organ of Corti as they move from the perilymph to the endolymph. The membrane covering the round window relaxes and expands when the vibrations hit it, helping to absorb the shock of impact.

Musical sounds are caused by rhythmical or regularly repeated vibrations, while irregular vibrations give rise to noises. In musical sounds loudness is determined by the height or amplitude of the vibrations, pitch by the length of the wave, and quality by the number of so called partial tones. A sensation of sound cannot be produced by [Pg 66] less than 30 vibrations a second and the ordinary person cannot hear more than 16,000 vibrations a second. Different sounds can be distinguished when they follow each other as closely as by one one-hundredth of a second.

Musical sounds are created by rhythmic or regularly repeated vibrations, whereas irregular vibrations produce noise. In musical sounds, loudness is determined by the height or amplitude of the vibrations, pitch by the length of the wave, and quality by the number of so-called partial tones. A sensation of sound cannot be produced by [Pg 66] fewer than 30 vibrations per second, and the average person cannot hear more than 16,000 vibrations per second. Different sounds can be distinguished when they follow each other as closely as one one-hundredth of a second apart.

All sound does not come through the canal of the ear. The bones of the head vibrate and carry sound. So there are instruments for the deaf which are put in the ear and others which are placed between the teeth.

All sound doesn’t just come through the ear canal. The bones in the head vibrate and transmit sound. So, there are devices for the deaf that can be placed in the ear and others that go between the teeth.

The semicircular canals are not essential to hearing but have something to do with a person’s power of maintaining his equilibrium. Injury to them may cause dizziness and loss of equilibrium.

The semicircular canals aren't crucial for hearing but are related to a person's ability to keep their balance. Damage to them can lead to dizziness and a loss of balance.

The Eye.—One more feature, perhaps the most expressive, remains to be described, the eye. The senses are all modifications of the original cutaneous sensibility and the nerve of sight is no more sensitive to light than any other nerve. It therefore needs an end organ that is sensitive to the motions of the ether in order to give impressions of light. This organ is provided in the eye, which is not only itself capable of being moved in every direction, but is placed in the most movable part of the body, the head, which can be turned in almost a complete circle. The eyeball is spherical and lies in the cavity of the orbit upon a cushion of fat, where it has a large range of sight but is securely protected from injury by its bony surroundings. The sunken eyes following protracted illness are due to the using by the system of the fat on which the eyeball ordinarily rests.

The Eye.—One more feature, perhaps the most expressive, remains to be described: the eye. All the senses are variations of the original skin sensitivity, and the optic nerve isn’t any more sensitive to light than any other nerve. It requires an end organ that can respond to the movement of light waves to convey visual information. This function is fulfilled by the eye, which can move in all directions and is situated in the most mobile part of the body, the head, capable of turning almost entirely around. The eyeball is spherical and rests in the orbital cavity on a cushion of fat, allowing for a wide range of vision while being well-protected from injury by the surrounding bone. The sunken eyes seen after prolonged illness result from the body using the fat that normally supports the eyeball.

Each orbital cavity is formed by the juncture of some seven bones and communicates with the cavity of the brain through the optic foramen and through the sphenoidal fissure. Above the orbits are arched eminences of skin, the eye-brows, from which several rows of short hairs grow longitudinally and which serve to protect the eyes and to limit the amount of light to a certain extent, as in frowning. [Pg 67]

Each orbital cavity is formed by the meeting of about seven bones and connects to the brain's cavity through the optic foramen and the sphenoidal fissure. Above the orbits are arched areas of skin, known as eyebrows, from which several rows of short hairs grow lengthwise. These hairs help protect the eyes and limit the amount of light that enters, especially when frowning. [Pg 67]

Still further protection is afforded by the eyelids, longitudinal folds of skin, the one above, the other below, which close like curtains over the eye. Beneath the external layer of skin in the lids is fatty tissue and then the orbicularis palpebrarum muscle by means of which they are closed. They are kept in shape by the tarsal plates or cartilages, in whose ocular surface are embedded the Meibomian glands, whose secretion prevents the free edges of the lids from sticking together. Along these edges grows a double or triple row of stiff hairs, the eye-lashes, which curve outward so as not to interfere with each other and also to prevent the entrance into the eye of foreign bodies. Lining the inner surface of the lids and reflected thence over the anterior surface of the sclerotic coat of the eye is a mucous membrane, the conjunctiva, which is thick, opaque, and vascular on the lids but thin and transparent on the eyeball. The angles between the lids are known as the internal and the external canthus.

Further protection is provided by the eyelids, which are folds of skin that close like curtains over the eye—one above and one below. Underneath the outer layer of skin in the lids is fatty tissue followed by the orbicularis palpebrarum muscle, which helps close them. They maintain their shape thanks to the tarsal plates or cartilages, which contain the Meibomian glands on their ocular surface. These glands produce a secretion that prevents the edges of the lids from sticking together. Along these edges are double or triple rows of stiff hairs called eye-lashes, which curve outward to avoid interfering with each other and also to keep foreign bodies from entering the eye. Lining the inner surface of the lids and extending over the front surface of the sclera is a mucous membrane known as the conjunctiva, which is thick, opaque, and vascular on the eyelids but thin and transparent on the eyeball. The corners where the lids meet are referred to as the internal and external canthus.

Fig. 23.—The external ocular muscles. (Pyle.)

Fig. 23.—The outer eye muscles. (Pyle.)

Muscles and Nerves.—The eyeball is held in position by the ocular muscles, the conjunctiva, and the lids, while surrounding it, yet allowing free movement, is a thin membranous sac, the tunica vaginalis oculi. The superior and inferior recti muscles at the upper and lower edges of the ball turn the eye up [Pg 68] and down; the internal and external recti at the inner and outer edges turn the eye inward and outward; and the superior and inferior oblique rotate the eye. The nerves supplying these muscles are the third or motor oculi, the fourth and the sixth.

Muscles and Nerves.—The eyeball is held in place by the eye muscles, the conjunctiva, and the eyelids, while a thin membranous sac, the tunica vaginalis oculi, surrounds it, allowing for free movement. The superior and inferior recti muscles at the top and bottom of the eyeball turn it up [Pg 68] and down; the internal and external rectus muscles at the inner and outer edges turn the eye inwards and outwards; and the superior and inferior oblique muscles rotate the eye. The nerves that control these muscles are the third or motor oculi, the fourth, and the sixth.

The lachrymal gland, which is about the size and shape of an almond, is situated at the upper and outer part of the orbit. It secretes a fluid which keeps the anterior surface of the eye bathed in moisture and is ordinarily drained away through the lachrymal sac in the inner canthus, whence it passes by the lachrymal ducts into the nose. When the amount secreted is excessive, it overflows the lower lid as tears.

The lachrymal gland, which is about the size and shape of an almond, is located at the upper outer part of the eye socket. It produces a fluid that keeps the front surface of the eye moist and is usually drained through the tear sac in the inner corner of the eye, from where it travels through the tear ducts into the nose. When too much fluid is produced, it spills over the lower eyelid as tears.

Fig. 24.—Diagram of the lacrimal apparatus. (Pyle.)

Fig. 24.—Diagram of the tear drainage system. (Pyle.)

Coats of Eye.—The membranes or coats of the eye are three in number: an outer or sclerotic, a middle or vascular, and an inner or sensitive.

Coats of Eye.—The membranes or layers of the eye are three in total: an outer layer called the sclera, a middle layer known as the choroid, and an inner layer that is sensitive.

The sclerotic coat is a rather thick, fibrous, protective membrane. Where it passes in front of the iris, however, it is thinner and transparent and is known as the cornea. The cornea projects somewhat and, as it were, resembles a segment of a smaller sphere set into the rest of the sclerotic.

The sclerotic coat is a fairly thick, fibrous protective layer. However, where it covers the iris, it becomes thinner and transparent, and it's called the cornea. The cornea sticks out a bit and resembles a part of a smaller sphere embedded in the rest of the sclerotic.

The middle or vascular coat, known as the choroid, carries blood-vessels for the retina or sensitive coat in its inner layer and has an outer layer of pigment cells that excludes light and darkens the inner chamber of the eye. The folds of the choroid at its anterior [Pg 69] margin contain the ciliary muscles and are known as the ciliary processes, while the name iris is given to the little round pigmented, perforated, curtain-like muscle just in front of the crystalline lens. The posterior surface of the iris is covered with a thick layer of pigment cells to prevent the entrance of light except through the central opening or pupil, and its anterior surface also has pigment cells that give it its color, though the difference in the color of people’s eyes is due rather to the amount of pigment present than to its color, a small amount of pigment being present in blue eyes and a large amount in brown and black eyes. Variations in the size of the pupil are brought about by contractions of the circular and radiating fibers of the iris, contraction of the circular fibers making it smaller and those of the radiating larger. The pupil is constricted for near objects and during sleep, and is dilated for distant objects. In a dull light also it dilates to let in more light, and in a bright light it contracts. The appearance of the pupil is often important as a means of diagnosis and in etherization.

The middle layer of the eye, called the choroid, contains blood vessels for the retina or sensitive layer in its inner part and has an outer layer of pigment cells that blocks light and darkens the inner chamber of the eye. The folds of the choroid at its front edge have the ciliary muscles and are referred to as the ciliary processes, while the term iris describes the small round pigmented muscle that looks like a curtain and is located just in front of the crystalline lens. The back surface of the iris is covered with a thick layer of pigment cells to stop any light from entering except through the central opening or pupil, and its front surface also has pigment cells that give it its color. The color variations in people's eyes are mainly due to the amount of pigment present rather than its hue; blue eyes have less pigment, while brown and black eyes have more. The size of the pupil changes due to the contractions of the circular and radiating fibers of the iris; the circular fibers make it smaller, while the radiating fibers make it larger. The pupil constricts for nearby objects and during sleep, and it dilates for distant objects. In dim light, it dilates to let in more light, and in bright light, it constricts. The appearance of the pupil is often significant for diagnosis and during anesthesia.

Fig. 25.—Vertical section through the eyeball and eyelids. (Pyle.)

Fig. 25.—Vertical section through the eyeball and eyelids. (Pyle.)

Lastly there is the innermost sensitive coat or retina, which has eight layers, the outer one containing some pigment cells and the next [Pg 70] the rods and cones, in which the power of perception is supposed to lie, branches of the optic nerve being distributed over it in all directions. In fact, the retina is formed by a membranous expansion of the optic or second cranial nerve, the special nerve of sight, which passes into the orbit through the optic foramen at the back and enters the eyeball close to the macula lutea or yellow spot. The exact spot where the optic nerve enters the retina is not sensitive and is known as the blind spot. In the center of the macula lutea, however, which is in the middle of the retina posteriorly, is a tiny pit, the fovea centralis, in which all the layers of the retina except the rods and cones are absent, and at this point vision is most perfect. It is, therefore, always turned toward the object looked at, and when one wishes to see an object distinctly, he must keep moving his eyes over it that the rays from each part may fall in turn upon the fovea centralis.

Lastly, there is the innermost sensitive coat or retina, which has eight layers. The outer layer contains some pigment cells, and the next layer has the rods and cones, where the ability to perceive images is believed to be located. Branches of the optic nerve spread out over it in all directions. In fact, the retina is made up of a membranous extension of the optic or second cranial nerve, which is the specialized nerve for sight. This nerve passes into the orbit through the optic foramen at the back and enters the eyeball near the macula lutea or yellow spot. The exact spot where the optic nerve enters the retina is not sensitive and is known as the blind spot. In the center of the macula lutea, which is at the back middle of the retina, there is a small pit called the fovea centralis, where all the layers of the retina except the rods and cones are absent, and vision is the sharpest. Therefore, it is always directed toward the object being viewed, and to see something clearly, one must keep moving their eyes over it so that rays from each part fall on the fovea centralis in turn.

Directly behind the pupil is the crystalline lens, a rather firm gelatinous body enclosed in a capsule, which is transparent in life but opaque in death. The lens is doubly convex and is held in place by the suspensory ligaments, which arise from the ciliary processes. In front of it is the anterior chamber of the eye, filled with a thin watery fluid called the aqueous humor, while the larger space back of it, occupying about four-fifths of the entire globe, is filled with a jelly-like substance known as the vitreous humor.

Directly behind the pupil is the crystalline lens, a firm, jelly-like body encased in a capsule that is clear when alive but cloudy after death. The lens is curved on both sides and is held in place by the suspensory ligaments, which come from the ciliary processes. In front of it is the anterior chamber of the eye, filled with a thin watery fluid called the aqueous humor, while the larger space behind it, taking up about four-fifths of the whole eye, is filled with a jelly-like substance known as the vitreous humor.

The chief artery of the eye is the ophthalmic.

The main artery of the eye is the ophthalmic.

Light Rays.—The eye is practically a camera and its principal function is to reflect images. Although there are several refracting surfaces and media, for practical purposes the cornea alone need be considered. Except for those rays which enter the eye perpendicularly to the cornea, whose line of entrance is called the optic axis, all rays are refracted when they enter the eye and the point at which they meet and cross each other behind the cornea is called the principal focus of the eye. To focus properly, all the rays from any one point [Pg 71] on an object must meet again in a common point upon the retina, their conjugate focus. In the normal eye all the rays from an object are focused on the retina and form upon it an image of the object which, as in the camera, is inverted, because of the crossing of the rays behind the cornea. Once focused on the retina the light traverses the various layers to the layer of rods and cones, where chemical action takes place and affects the little filaments of the optic nerve, by which the message is carried to the brain.

Light Rays.—The eye works like a camera, and its main job is to capture images. Even though there are several surfaces and materials that bend light, we only need to focus on the cornea for practical reasons. Except for the rays that enter the eye straight on, which follow the optic axis, all other rays get bent when they enter, and the spot where they intersect behind the cornea is known as the principal focus of the eye. For proper focusing, all rays from a single point on an object must converge at a single point on the retina, known as their conjugate focus. In a healthy eye, all rays from an object focus on the retina and create an image of the object that is upside down, just like in a camera, due to the crossing of the rays behind the cornea. After being focused on the retina, the light passes through various layers to reach the layer of rods and cones, where a chemical reaction occurs and stimulates the tiny fibers of the optic nerve, which then sends the message to the brain.

Fig. 26.—Diagram showing the difference between (A) emmetropic, (B) myopic and (C) hypermetropic eyes. (American Text-book of Physiology.)

Fig. 26.—Diagram illustrating the differences between (A) normal vision, (B) nearsightedness, and (C) farsightedness. (American Text-book of Physiology.)

When the eye is at rest the pupil and lens are in their normal [Pg 72] condition and at such times the eye sees only distant objects. The ability of the eye to focus upon objects at different distances is called accommodation and to accomplish it three things are necessary: 1. change in the shape of the lens; 2. convergence of the axes of the eyes, and 3. narrowing of the pupils.

When the eye is at rest, the pupil and lens are in their normal condition, and at that time, the eye only sees distant objects. The eye's ability to focus on objects at various distances is called accommodation, and to achieve this, three things are needed: 1. a change in the shape of the lens; 2. convergence of the axes of the eyes; and 3. narrowing of the pupils.

When the eye is directed toward distant objects, the muscle fibers in the ciliary processes relax, causing tightening of the suspensory ligaments and consequent flattening of the surface of the lens. Otherwise an image would be formed in front of the retina; for the greater the convexity of the lens, the greater the angle of refraction. Such accommodation is passive and so not fatiguing. To look at nearby objects, on the contrary, the ciliary muscles contract, drawing the choroid forward and allowing the suspensory ligaments to relax, so that the lens bulges in front. This is an exertion.

When the eye focuses on distant objects, the muscle fibers in the ciliary processes relax, which tightens the suspensory ligaments and flattens the lens surface. Otherwise, an image would be formed in front of the retina; the more curved the lens, the greater the angle of refraction. This adjustment is passive and not tiring. In contrast, when looking at nearby objects, the ciliary muscles contract, pulling the choroid forward and allowing the suspensory ligaments to relax, making the lens bulge out. This requires effort.

In order to accommodate properly, moreover, both eyes must work together and the axes of both eyes must be directed toward the object. Therefore, in looking at nearby objects the axes of the eyes converge, drawn by the internal recti muscles. In strabismus or cross eye, where the axes of both eyes cannot be directed toward the object at the same time, the rays fall upon one part of one eye and upon a different part of the other eye and two separate images are seen.

To properly accommodate, both eyes need to work together, and the axes of both eyes must point toward the object. So, when looking at close objects, the axes of the eyes converge, pulled by the internal rectus muscles. In strabismus or crossed eyes, where the axes of both eyes can't focus on the object at the same time, the light rays hit one part of one eye and a different part of the other eye, resulting in two separate images being seen.

Finally there is concentric narrowing of the pupil by contraction of the circular fibers of the iris, by which means various side rays that would come to a focus outside the retina are excluded.

Finally, the pupil narrows concentrically as the circular fibers of the iris contract, which helps to eliminate various side rays that would focus outside the retina.

All the muscles of accommodation, the ciliary muscles, the internal recti, and the sphincter pupillæ, are under the control of the third nerve.

All the muscles that help the eyes focus, including the ciliary muscles, the internal rectus muscles, and the pupil's sphincter muscle, are controlled by the third cranial nerve.

Connected with this power of accommodation and dependent on it are the two conditions of near-sightedness or myopia and far-sightedness or hypermetropia.

Connected with this ability to adjust and relying on it are the two conditions of nearsightedness or myopia and farsightedness or hypermetropia.

The normal eye is emmetropic and is almost perfectly spherical, but in [Pg 73] the near-sighted or myopic eye the ball, instead of being round, is flattened from above down and so bulges in front. Consequently, owing to the greater distance from the lens to the retina, images are formed in front of the retina. Only nearby objects can be seen clearly, because the farther the object from the eye the farther in front of the retina the image is formed. Concave glasses are worn to enable near-sighted people to see at a distance. Hypermetropic or far-sighted eyes are flattened from before backward and can see only objects at a distance clearly, as those nearby form images behind the retina. For such eyes convex glasses are worn.

The normal eye is emmetropic and is almost perfectly spherical, but in [Pg 73] a near-sighted or myopic eye, the shape is not round; it is flattened from top to bottom and bulges at the front. As a result, because the distance from the lens to the retina is greater, images form in front of the retina. Only nearby objects can be seen clearly, since the farther away an object is, the further in front of the retina the image appears. Near-sighted people wear concave glasses to help them see distant objects. Hypermetropic or far-sighted eyes are flattened from front to back and can only see distant objects clearly, as those nearby create images behind the retina. For these eyes, convex glasses are worn.

As the ordinary person approaches middle life, he becomes able to see better at a distance than near to. This presbyopia, as it is called, which is practically far-sightedness, is due to a partial loss of the power of accommodation in the lens, the result of a general loss of elasticity in the parts.

As a typical person reaches middle age, they find that their distance vision is better than their close-up vision. This presbyopia, as it’s known, is essentially far-sightedness caused by a partial decline in the lens's ability to adjust, resulting from a general decrease in elasticity in those areas.

Another very common defect is astigmatism, a failure of the rays to focus upon a point, owing generally to a flattening in the surface of the cornea.

Another very common issue is astigmatism, which occurs when light rays don't focus on a single point, typically because the surface of the cornea is flattened.

Color perception is also an important function of the eye. The waves of hyperluminous ether when of a certain rate of vibration give the sensation of heat and when their vibrations are more rapid they give the sensation of light. Each of the primary colors of the spectrum gives off a pretty definite number of light rays which travel through the air and enter the eye, the number of rays determining the color thrown upon the retina and the velocity determining the intensity of the color. Occasionally when light is passing through into the eye it is broken up as in a prism and the person gets a sensation as of all sorts of colors, chromatic aberration. Total or partial absence of sensitiveness to color is called color blindness. It is commonest in the form of inability to distinguish between red and green and is probably due to a defect in the retina. [Pg 74]

Color perception is an essential function of the eye. The waves of hyperluminous ether, when vibrating at a certain frequency, produce the sensation of heat, and when their vibrations are faster, they create the sensation of light. Each primary color of the spectrum emits a specific number of light rays that travel through the air and enter the eye, with the quantity of rays determining the color reflected on the retina and the speed affecting the intensity of the color. Sometimes when light enters the eye, it is dispersed like in a prism, making the person perceive various colors, chromatic aberration. A complete or partial inability to perceive colors is known as color blindness. The most common type of this condition is the inability to differentiate between red and green, which is likely caused by a defect in the retina. [Pg 74]

Sometimes a hair follicle on the lid becomes infected and a sty is formed. Pink eye is conjunctivitis or inflammation of the conjunctiva. A Meibomian duct may become stopped and cause bulging, or there may be a sagging down or ptosis of the upper lid in certain diseases, as meningitis, apoplexy, and more especially syphilis. Rodent ulcer often begins by the eye or on the cheek.

Sometimes a hair follicle on the eyelid gets infected and a sty forms. Pink eye refers to conjunctivitis or inflammation of the conjunctiva. A Meibomian duct can get blocked, leading to swelling, or there might be drooping, or ptosis of the upper lid, in certain conditions like meningitis, stroke, and especially syphilis. Rodent ulcer often starts near the eye or on the cheek.


CHAPTER V.
The Nervous System.

The nervous system, which regulates all the vital processes of the body, physical and chemical, and which is situated partly in the head and partly in the trunk, may well form the connecting link between the description of the head and that of the trunk. It has two divisions, the cerebro-spinal system and the sympathetic system. The former consists of the cerebrum or brain proper, the cerebellum or little brain, the pons Varolii, the medulla oblongata, the spinal cord, and the cranial and spinal nerves; the latter of a series of ganglia or aggregations of nerve centers. The brain, which includes the cerebrum, cerebellum, pons, and medulla, occupies the cranium and the spinal cord is contained within the bony framework of the spinal column. In the male the brain weighs about 49 ounces and in the female 44, while in an idiot it seldom weighs more than 23 ounces.

The nervous system, which controls all the essential processes of the body, both physical and chemical, is located partly in the head and partly in the trunk, making it a good connection between the head and the trunk descriptions. It has two parts: the cerebro-spinal system and the sympathetic system. The first includes the cerebrum (the primary brain), the cerebellum (the small brain), the pons Varolii, the medulla oblongata, the spinal cord, and the cranial and spinal nerves; the second consists of a series of ganglia or clusters of nerve centers. The brain, which includes the cerebrum, cerebellum, pons, and medulla, is located in the skull, while the spinal cord is found within the bony structure of the spinal column. In males, the brain weighs about 49 ounces, and in females, it weighs about 44 ounces; in people with severe intellectual disabilities, it rarely exceeds 23 ounces.

The cerebrum or brain proper has two parts or hemispheres, roughly oval in shape, each of which has five lobes separated by fissures, the frontal, parietal, occipital, and temporo-sphenoidal lobes, and the central lobe or island of Reil at the base of the brain. The chief fissures are the longitudinal fissure, the fissure of Sylvius at the base of the brain, and the fissure of Rolando between the frontal and parietal lobes. There are also five serous cavities called ventricles, the two lateral and the third, fourth, and fifth ventricles, of which the first two, one in either hemisphere, are the most important. Around these cavities is the brain substance, which is made up of two tissues, the white and the gray, the latter [Pg 76] forming the outer part of the brain to the depth of perhaps half an inch, and the white matter forming the rest. The outer or gray part is called the cortex and is largely made up of nerve cells. It might be called the active part of the brain. The white part consists largely of nerve fibers which are given off from the nerve cells and are carried down into the spinal cord.

The cerebrum or brain has two parts or hemispheres, roughly oval in shape, each with five lobes separated by grooves: the frontal, parietal, occipital, and temporo-sphenoidal lobes, plus the central lobe or island of Reil at the base of the brain. The main grooves are the longitudinal fissure, the fissure of Sylvius at the base of the brain, and the fissure of Rolando between the frontal and parietal lobes. There are also five fluid-filled spaces called ventricles: the two lateral ones, and the third, fourth, and fifth ventricles, with the first two, one in each hemisphere, being the most important. Surrounding these spaces is the brain substance, made up of two types of tissue: white and gray matter, with the gray matter forming the outer layer of the brain to a depth of about half an inch, and the white matter making up the rest. The outer or gray part is known as the cortex and is mostly composed of nerve cells. It can be considered the active part of the brain. The white matter mainly consists of nerve fibers that extend from the nerve cells down into the spinal cord.

The surface of the brain is convoluted, the ridges being separated by deep furrows or sulci, by which means a great extent of gray matter is secured. The furrows contain fluid from the subarachnoid spaces and vary in number and depth according to intelligence. While the convolutions are not uniform in all brains, the principal ones are constant.

The surface of the brain is folded, with ridges separated by deep grooves or sulci, allowing for a large amount of gray matter. These grooves contain fluid from the subarachnoid spaces and their number and depth vary with a person's intelligence. Although the folds aren't the same in every brain, the main ones are consistent.

Both the brain and the spinal cord are covered by three membranes, the dura mater, the arachnoid, and the pia mater. The dura mater is dense and fibrous and lines the interior of the skull, being firmly adherent to it at many points. In fact, it constitutes the internal periosteum of the cranial bones. The arachnoid is a delicate serous membrane, with two layers, lubricated to prevent friction, which divides the space between the dura mater and the pia mater, bridging over the convolutions and enclosing the subdural and subarachnoid spaces which are connected with lymphatics and contain a serous secretion, the cerebro-spinal fluid. This fluid forms an elastic water cushion, on which the brain rests, and prevents concussion. The pia mater is vascular, containing blood-vessels, lymphatics, and nerves, and is closely attached to the surface of the brain, dipping down into all the sulci.

Both the brain and the spinal cord are protected by three membranes: the dura mater, the arachnoid, and the pia mater. The dura mater is tough and fibrous, lining the inside of the skull and sticking to it at many points. It's actually the internal periosteum of the cranial bones. The arachnoid is a delicate membrane with two layers, which are lubricated to reduce friction. It creates a space between the dura mater and pia mater, bridging over the folds of the brain and enclosing the subdural and subarachnoid spaces that are linked to lymphatics and contain a fluid called cerebro-spinal fluid. This fluid acts as a protective cushion, supporting the brain and helping to prevent concussions. The pia mater is vascular, filled with blood vessels, lymphatics, and nerves, and it closely follows the surface of the brain, dipping into all the grooves.

At the base or under surface of the brain are some very important structures. The olfactory bulbs lie beneath the frontal lobe and projecting back is the olfactory tract, through which the olfactory nerves come from the brain. Back of the olfactory tract is the optic commissure where the optic nerves coming from the brain cross each other. And back of the commissure again is the optic tract, where the [Pg 77] optic nerves emerge from the brain. At the base of the brain are also the exits of the twelve cranial nerves.

At the base or underside of the brain are some very important structures. The olfactory bulbs are located beneath the frontal lobe, and projecting backward is the olfactory tract, which carries the olfactory nerves from the brain. Behind the olfactory tract is the optic commissure where the optic nerves from the brain cross each other. Further back from the commissure is the optic tract, where the [Pg 77] optic nerves exit the brain. At the base of the brain are also the exits for the twelve cranial nerves.

Fig. 27.—Base of brain. (Leidy.) 1, 2, 3, cerebrum; 4 and 5, longitudinal fissure; 6, fissure of Sylvius; 7, anterior perforated spaces; 8, infundibulum; 9, corpora albicantia; 10, posterior perforated space; 11, crura cerebri; 12, pons Varolii; 13, junction of spinal cord and medulla oblongata; 14, anterior pyramid; 14ˣ, decussation of anterior pyramid; 15, olivary body; 16, restiform body; 17, cerebellum; 19, crura cerebelli; 21, olfactory sulcus; 22, olfactory tract; 23, olfactory bulbs; 24, optic commissure; 25, motor oculi nerve; 26, patheticus nerve; 27, trigeminus nerve; 28, abducens nerve; 29, facial nerve; 30, auditory nerve; 31, glosso-pharyngeal nerve; 32, pneumogastric nerve; 33, spinal accessory nerve; 34, hypoglossal nerve.

Fig. 27.—Base of brain. (Leidy.) 1, 2, 3, cerebrum; 4 and 5, longitudinal fissure; 6, Sylvian fissure; 7, anterior perforated spaces; 8, infundibulum; 9, corpora albicantia; 10, posterior perforated space; 11, cerebral peduncles; 12, pons Varolii; 13, junction of spinal cord and medulla oblongata; 14, anterior pyramid; 14ˣ, decussation of anterior pyramid; 15, olivary body; 16, restiform body; 17, cerebellum; 19, cerebellar peduncles; 21, olfactory sulcus; 22, olfactory tract; 23, olfactory bulbs; 24, optic commissure; 25, oculomotor nerve; 26, trochlear nerve; 27, trigeminal nerve; 28, abducens nerve; 29, facial nerve; 30, auditory nerve; 31, glossopharyngeal nerve; 32, vagus nerve; 33, spinal accessory nerve; 34, hypoglossal nerve.

Upon entering the brain the arteries run a tortuous course, the tortuosity breaking the force of the blood stream in the small vessels where congestion would be with difficulty relieved. The basilar artery, which is formed by the juncture of the two vertebrals, divides into the [Pg 78] two posterior cerebrals, each of which joins one of the anterior cerebrals by a posterior communicating artery. The two anterior cerebrals also are joined by an anterior communicating artery, thus completing the circle. The circle thus formed at the base of the brain is called the circle of Willis and provides for a good supply of blood in event of an accident to any vessel. The blood is returned to the general circulation through the cerebral veins and sinuses formed by the separation of the dura mater into two layers.

Upon entering the brain, the arteries take a winding path, which helps reduce the pressure of the blood flow in the small vessels, where any blockage would be hard to clear. The basilar artery, formed by the joining of the two vertebral arteries, splits into the [Pg 78] two posterior cerebral arteries, each connecting to one of the anterior cerebral arteries via a posterior communicating artery. The two anterior cerebral arteries are also connected by an anterior communicating artery, completing the circle. This circle at the base of the brain is known as the circle of Willis and ensures a good blood supply if any vessel is damaged. The blood is returned to general circulation through the cerebral veins and sinuses created by the splitting of the dura mater into two layers.

The cerebellum is about one-seventh the size of the cerebrum and weighs about 5 ounces. It lies in the lower occipital fossæ of the skull and is oblong in shape and divided into two lateral hemispheres by a transverse fissure. It is made up of both white and gray matter, of which the former predominates, the gray being external as in the cerebrum. The cells are about the same as in the cortex and its surface is traversed by queer furrows. Of its function little is known but it probably plays a most important part in the coördination of the nervous and muscular acts by which the movements of the body are carried on.

The cerebellum is roughly one-seventh the size of the cerebrum and weighs about 5 ounces. It is located in the lower occipital fossæ of the skull, has an oblong shape, and is divided into two lateral hemispheres by a transverse fissure. It consists of both white and gray matter, with white matter being more prevalent, while the gray matter is on the outside, similar to the cerebrum. The cells are comparable to those in the cortex, and its surface has unusual grooves. Its function is not well understood, but it likely plays a crucial role in coordinating the nervous and muscular actions that facilitate body movements.

At the back of the cerebrum and below the cerebellum is the pons Varolii, which forms a connecting link with the medulla oblongata or bulging part of the cord. It is made up essentially of white matter or nerve fibers, though there is a small amount of gray matter in which are found the nuclei of some of the cranial nerves.

At the back of the brain and beneath the cerebellum is the pons Varolii, which connects to the medulla oblongata, the bulging part of the spinal cord. It's primarily made up of white matter, or nerve fibers, although there's a small amount of gray matter that contains the nuclei of some cranial nerves.

In the medulla oblongata, which is about 1 inch long and extends from the pons Varolii to the upper border of the atlas or first cervical vertebra, the gray matter is not necessarily external to the white but is found in patches in the white. The gray matter here corresponds more or less to that of the spinal cord and the white matter is continuous with that of the cord. From the medulla arise the fifth to twelfth cranial nerves and the vasomotor nerves. The cardiac nerve has its center here and here too are the centers of respiration, [Pg 79] phonation, deglutition, mastication, and expression. In the medulla the nerves that arise in the cerebrum cross over from one side of the body to the other on the crossed pyramidal tracts. The importance of this crossing of the nerve fibers is seen in apoplexy, when a blood-vessel is ruptured in the brain and hemorrhage causes pressure, generally on the motor tract. Paralysis of the nerves and of the muscles to which they go results. The paralysis is generally of one side of the body, the opposite side from that on which the injury occurred. The seat of injury in the brain or cord can frequently be determined by the situation and extent of the paralysis.

In the medulla oblongata, which is about 1 inch long and stretches from the pons Varolii to the upper edge of the atlas or first cervical vertebra, the gray matter isn’t always on the outside of the white matter but is found in patches within it. The gray matter here corresponds to that of the spinal cord, and the white matter is continuous with that of the cord. The fifth to twelfth cranial nerves and the vasomotor nerves originate from the medulla. The cardiac nerve has its center here, as do the centers for breathing, speaking, swallowing, chewing, and expressing emotions. In the medulla, the nerves that come from the cerebrum cross from one side of the body to the other on the crossed pyramidal tracts. The significance of this crossing of nerve fibers is evident in cases of stroke, when a blood vessel ruptures in the brain, causing bleeding that puts pressure, usually on the motor tract. This leads to paralysis of the nerves and the muscles they connect to. Typically, the paralysis affects one side of the body, the opposite side from where the injury happened. The location and extent of the paralysis can often help determine where the injury occurred in the brain or spinal cord.

Spinal Cord.—Extending down from the medulla through the spinal column is the cord. Its length from the foramen magnum, where it begins, down through the vertebræ to the lower border of the first lumbar vertebra, where it ends in a very fine thread-like process with no special function, called the filum terminale, is 17 to 18 inches. Just before it ends a number of nerves are given off in a tail-like expansion known as the cauda equina or horse’s tail. It is not uniform throughout its length but presents two enlargements, a cervical enlargement in the lower cervical region, and a lumbar enlargement in the lower dorsal region, where the nerves are given off to the arms and legs respectively. The membranes are the same as those of the brain and are continuous with them, but here the dura mater is not attached to the bony walls enclosing it. For the cord does not fit closely into the canal but is as it were suspended in it. The subarachnoid space communicates with the ventricles of the brain by the foramen of Majendie and is filled with cerebro-spinal fluid for the protection of the cord. In cerebro-spinal meningitis or spotted fever this fluid is infected and for diagnosis lumbar puncture is performed. [Pg 80]

Spinal Cord.—Extending down from the medulla through the spinal column is the spinal cord. Its length from the foramen magnum, where it begins, down through the vertebrae to the lower edge of the first lumbar vertebra, where it ends in a thin, thread-like structure with no specific function called the filum terminale, is 17 to 18 inches. Just before it ends, several nerves are given off in a tail-like expansion known as the cauda equina or horse's tail. The spinal cord isn't uniform along its length; it has two enlargements, a cervical enlargement in the lower cervical region and a lumbar enlargement in the lower thoracic region, where the nerves that serve the arms and legs are given off. The membranes are the same as those of the brain and are continuous with them, but here the dura mater isn't attached to the bony walls that enclose it. The cord doesn't fit tightly into the canal but is somewhat suspended within it. The subarachnoid space connects to the ventricles of the brain via the foramen of Majendie and is filled with cerebro-spinal fluid for the protection of the cord. In cases of cerebro-spinal meningitis or spotted fever, this fluid becomes infected, and a lumbar puncture is performed for diagnosis. [Pg 80]

Fig. 28.—Different views of a portion of the spinal cord from the cervical region, with the roots of the nerves. In A the anterior surface of the specimen is shown, the anterior nerve root of its right side being divided; in B a view of the right side is given; in C the upper surface is shown; in D the nerve roots and ganglion are shown from below: 1, the anterior median fissure; 2, posterior median fissure; 3, anterior lateral depression, over which the anterior nerve roots are seen to spread; 4, posterior lateral groove, into which the posterior roots are seen to sink; 5, anterior roots passing the ganglion; 5´, in A, the anterior root divided; 6, the posterior roots, the fibers of which pass into the ganglion, 6; 7, the united or compound nerve; 7´, the posterior primary branch seen in A and D to be derived in part from the anterior and in part from the posterior root. (Allen Thomson.)

Fig. 28.—Different views of a section of the spinal cord from the cervical area, showing the nerve roots. In A, the front side of the specimen is displayed, with the anterior nerve root on its right side cut; in B, a view of the right side is provided; in C, the top surface is shown; in D, the nerve roots and ganglion are illustrated from below: 1, the anterior median fissure; 2, posterior median fissure; 3, anterior lateral depression, over which the anterior nerve roots spread; 4, posterior lateral groove, into which the posterior roots descend; 5, anterior roots passing the ganglion; 5´, in A, the anterior root that is cut; 6, the posterior roots, the fibers of which enter the ganglion, 6; 7, the united or compound nerve; 7´, the posterior primary branch seen in A and D derived partly from the anterior and partly from the posterior root. (Allen Thomson.)

If a cross-section of the cord is made, it is found to have a pretty definite structure. It is roughly circular and is divided by certain fissures, of which the most important are the anterior and posterior median, the latter being rather a dividing line or septum. By them it is divided into halves connected by a small band in the middle called the commissure. The white matter is exterior to the gray and is divided by it into four columns, which again are divided into tracts according to certain groups of nerves that travel through them. The most important tract is the direct pyramidal tract in the anterior column. The gray matter is arranged in the form of a letter H practically, consisting of two lateral halves, more or less crescentic in outline, connected by a narrow band, the gray commissure. Each half is divided into two horns, the anterior, toward the front of the cord, and the posterior, toward the back, the former being generally much thicker and heavier than the latter. The structure of the gray and [Pg 81] of the white matter is essentially the same as in the brain, but the proportion varies in different parts of the cord, the white predominating in the cervical region and the gray being much better developed in the lumbar region, where the nerve cells for control of the lower extremities occur. The gray is least well developed in the dorsal region. Through the center of the cord runs a small hole or canal filled with cerebro-spinal fluid, the central canal of the cord.

If you take a cross-section of the spinal cord, you'll see it has a pretty distinct structure. It’s roughly circular and divided by certain fissures, with the most important ones being the anterior and posterior median, the latter serving more as a dividing line or septum. These fissures split it into halves connected by a small band in the middle called the commissure. The white matter surrounds the gray matter and is divided by it into four columns, which are further divided into tracts based on specific groups of nerves that pass through them. The most notable tract is the direct pyramidal tract in the anterior column. The gray matter is arranged like a letter H, consisting of two lateral halves that are somewhat crescent-shaped, connected by a narrow band known as the gray commissure. Each half has two horns: the anterior, located toward the front of the cord, and the posterior, toward the back, with the anterior generally being thicker and heavier than the posterior. The structure of the gray and [Pg 81] white matter is basically the same as in the brain, though the proportions vary in different parts of the cord, with white matter dominating in the cervical region and gray matter being more developed in the lumbar region, where the nerve cells control the lower limbs. The gray matter is least developed in the dorsal region. In the center of the cord runs a small hole or canal filled with cerebrospinal fluid, known as the central canal of the cord.

Fig. 29.—Functional areas of the cerebral cortex, left hemisphere. (A. A. Stevens.)

Fig. 29.—Functional areas of the cerebral cortex, left hemisphere. (A. A. Stevens.)

The brain is the seat of intelligence and will, the center of all voluntary action. Molecular change in some part of the cerebral substance is the indispensable accompaniment of every phenomenon of consciousness. Indeed, the brain is never in a state of complete repose, there being dreams even during sleep. The brain is not sensitive to injury in the sense of pain. It can be lacerated without much pain.

The brain is where intelligence and will reside, and it’s the hub of all voluntary actions. Any change at the molecular level in some part of the brain is essential for every conscious experience. In fact, the brain is never completely still, as it even experiences dreams while we sleep. The brain doesn’t feel pain in the way other parts of the body do. It can be damaged without causing much pain.

Various centers exist in the brain, of which the most important perhaps is the motor center. The visual center is in the occipital lobe, [Pg 82] the auditory center in the temporal lobe, the speech center in the third left frontal convolution. Thus the impulses of the senses have been located, though the function of many parts, the so called silent areas, are still in obscurity.

Various centers exist in the brain, with the most important likely being the motor center. The visual center is in the occipital lobe, [Pg 82] the auditory center is in the temporal lobe, and the speech center is in the third left frontal convolution. So, we've pinpointed where the sensory impulses come from, but the functions of many areas, known as the silent areas, are still unclear.

The motor center, that is, the center for motion of the skeletal muscles, is situated about the fissure of Rolando and is divided into three parts, one for the legs, one for the face, and one for the arms, the one for the legs being uppermost and the others below in the order mentioned. Fibers from these cells extend down through the brain and cord to the muscles, the fibers being collected into well-recognized bundles and the whole known as the motor tract. There may be one long fiber from a cell in the brain down through most of the cord or there may be a succession of shorter fibers that are not actually connected but are in close contact with each other. In the upper pons the fibers for the face cross to the opposite side, while the rest keep on down through the medulla, and as they emerge from the medulla they too cross to the other side and keep on down in the crossed pyramidal tract. A few fibers do not cross but come down the direct pyramidal tract, which, however, disappears part way down. The crossed pyramidal tract is the true motor tract and in it the fibers are continually sending branches to the cells in the gray matter, where they connect with the anterior horn.

The motor center, which is the center for movement of the skeletal muscles, is located around the fissure of Rolando and is divided into three sections: one for the legs, one for the face, and one for the arms, with the leg section being at the top and the others arranged below in that order. Fibers from these cells extend down through the brain and spinal cord to the muscles, with the fibers grouped into well-known bundles collectively referred to as the motor tract. There can be one long fiber from a cell in the brain that goes through most of the spinal cord, or there can be a series of shorter fibers that aren’t directly connected but are in close proximity to one another. In the upper pons, the fibers for the face cross over to the opposite side, while the others continue down through the medulla, and as they exit the medulla, they also cross over to the other side and continue down in the crossed pyramidal tract. A few fibers don’t cross and travel down the direct pyramidal tract, which, however, disappears partway down. The crossed pyramidal tract is the primary motor tract, and within it, the fibers are continuously sending branches to the cells in the gray matter, where they connect with the anterior horn.

The anatomy of the sensory tract is not so well understood. By it impulses are sent to the brain by the peripheral organs, practically the surface of the body. The sensory fibers connect with the sensory cells in the posterior horn, from which fibers are sent to the brain, practically the reverse of motor action. There are three chief sensory tracts, which are supposed to transmit different sensations, one pain, one muscular sensations, and the third sensations of touch. All these tracts, of which the chief is the direct cerebellar tract, in passing up the cord pass to the opposite side at different levels and then go on to the cortex of the brain. [Pg 83]

The anatomy of the sensory tract isn’t fully understood. This tract sends impulses to the brain from the peripheral organs, essentially from the surface of the body. The sensory fibers connect with the sensory cells in the posterior horn, which then send fibers to the brain, almost the opposite of how motor action works. There are three main sensory tracts, each believed to transmit different sensations: one for pain, one for muscle sensations, and the third for touch. All these tracts, with the main one being the direct cerebellar tract, cross to the opposite side of the cord at different levels and then continue on to the brain's cortex. [Pg 83]

The action of the nerves is similar to reflex action, only that an effort of will is needed to send an impulse from the brain. It is by the help of the brain along this line that an infinity of artificial reflexes or habits is acquired, for which volition is needed in the beginning but which are later done unconsciously. Herein lie the possibilities of all education.

The way nerves work is similar to reflex actions, except that you need to consciously decide to send an impulse from the brain. It's with the brain's help in this process that we develop countless artificial reflexes or habits—initially requiring willpower but eventually performed automatically. This is where all educational opportunities come into play.

The brain and spinal cord work together, the cord acting as a medium between the brain, in which all the higher psychical processes, such as will, thought, etc., originate, and the muscular apparatus. The cord, however, has some action entirely independent of the brain, as is seen in reflex action. This action is entirely involuntary, so that the cord is sometimes spoken of as the seat of involuntary action, commonly called reflex action. All unconscious acts are reflex acts, as when the hand is drawn away from a hot iron. If an impulse is sent along one of the sensory fibers, it enters the cord through the posterior horn, where its nerve cell is found. Then, through some connection between the nerve cell of the sensory fiber and that of the motor fiber the impulse is transmitted to the motor cell and another impulse is sent out of the cord along the motor fiber of the nerve to the muscle. One of the commonest reflexes is the knee-jerk. Reflex action is important because the reflexes are interfered with, delayed, destroyed, or increased in different diseases. The time normally required for a reflex act is very brief, that for the knee-jerk being about three one-hundredths of a second.

The brain and spinal cord work together, with the spinal cord acting as a link between the brain, where all higher mental processes like will and thought originate, and the muscular system. However, the spinal cord can also operate independently of the brain, as seen in reflex actions. These actions are completely involuntary, which is why the cord is sometimes referred to as the center of involuntary actions, commonly known as reflex actions. All unconscious acts are reflex acts, like when your hand pulls away from a hot iron. When an impulse travels along one of the sensory fibers, it enters the spinal cord through the posterior horn, where its nerve cell is located. Then, through a connection between the nerve cell of the sensory fiber and that of the motor fiber, the impulse is relayed to the motor cell, and another impulse is sent out of the spinal cord along the motor fiber to the muscle. One of the most common reflexes is the knee-jerk. Reflex actions matter because they can be disrupted, delayed, destroyed, or heightened in various diseases. The typical time required for a reflex action is very short, with the knee-jerk reflex taking about three one-hundredths of a second.

The nerves of the head, known as the cranial nerves, arise from the brain, while the rest of the body is supplied by the spinal nerves, which come off at intervals from the spinal cord. The cranial nerves consist of twelve pairs: (1) The olfactory or nerve of smell, (2) the optic or nerve of sight, (3) the motor oculi, (4) the patheticus, which controls the eye, (5) the trigeminus or trifacial, a nerve of general sensation, motion, and taste, (6) the abducens, a motor nerve, (7) the [Pg 84] facial nerve of the face, ear, palate, and tongue, (8) the auditory or nerve of hearing, (9) the glosso-pharyngeal, nerve of sensation and taste, (10) the pneumogastric or vagus, which is both motor and sensory and governs respiration, the heart, and the stomach, (11) the spinal accessory, to the muscles of the soft palate, and (12) the hypoglossal, the motor nerve to the tongue.

The nerves in the head, called the cranial nerves, come from the brain, while the rest of the body is connected by the spinal nerves, which branch off at intervals from the spinal cord. There are twelve pairs of cranial nerves: (1) The olfactory nerve, responsible for smell, (2) the optic nerve, responsible for sight, (3) the oculomotor, (4) the trochlear, which controls eye movement, (5) the trigeminal nerve, which is involved in sensation, movement, and taste, (6) the abducens, a motor nerve, (7) the facial nerve, which serves the face, ear, palate, and tongue, (8) the auditory nerve, responsible for hearing, (9) the glossopharyngeal nerve, which handles sensation and taste, (10) the vagus nerve, which is both motor and sensory and regulates breathing, the heart, and the stomach, (11) the accessory nerve, which connects to the muscles of the soft palate, and (12) the hypoglossal nerve, the motor nerve for the tongue.

The spinal nerves also are arranged in pairs: Eight cervical pairs, twelve dorsal or thoracic, five lumbar, five sacral, and one coccygeal, these titles denoting their point of origin near the vertebra of the same name. Each of these nerves arises by two roots, an anterior motor root from the anterior horn of gray matter and a posterior sensory root from the posterior horn, the latter having a ganglion upon it. After emerging from the cord the two roots unite to form the nerve, that the nerve may contain both motor and sensory fibers. The motor fibers are called efferent because they carry impulses from the cord, while the sensory are called afferent because they carry impulses back to the cord. After leaving the cord the nerves unite to form plexuses, which again divide into various nerve trunks and are distributed to the muscles.

The spinal nerves are arranged in pairs: eight cervical pairs, twelve dorsal or thoracic, five lumbar, five sacral, and one coccygeal, with these names indicating their origin near the corresponding vertebrae. Each of these nerves has two roots: an anterior motor root from the front part of the gray matter and a posterior sensory root from the back part, the latter having a ganglion on it. Once they exit the spinal cord, the two roots join together to form the nerve, allowing it to carry both motor and sensory fibers. The motor fibers are referred to as efferent because they transmit signals from the spinal cord, while the sensory fibers are called afferent because they send signals back to the spinal cord. After leaving the cord, the nerves join to create plexuses, which then branch out into various nerve trunks that supply the muscles.

The first cervical nerves pass out of the spinal column above the first cervical vertebra and the other cervical nerves below that and the succeeding vertebræ, while the other spinal nerves emerge each below the corresponding vertebra, as the first dorsal below the first dorsal vertebra, etc. After emerging they break up into a large anterior division and a small posterior division, the posterior branches supplying the spine and the dorsal muscles and skin, the anterior the rest of the trunk and the limbs. The cervical plexus is formed by the anterior divisions of the first four cervical nerves, the brachial plexus by the last four cervical and the first dorsal or thoracic nerves, the lumbar plexus by the four upper lumbar, and the sacral plexus by the last lumbar and the four upper sacral nerves. [Pg 85]

The first cervical nerves exit the spinal column above the first cervical vertebra, while the other cervical nerves exit below that and the following vertebrae. In contrast, the other spinal nerves come out below their corresponding vertebrae, like the first dorsal nerve coming out below the first dorsal vertebra, and so on. Once they emerge, they split into a large anterior division and a smaller posterior division, with the posterior branches supplying the spine and the dorsal muscles and skin, and the anterior division supplying the rest of the trunk and limbs. The cervical plexus is made up of the anterior divisions of the first four cervical nerves, the brachial plexus consists of the last four cervical nerves and the first dorsal or thoracic nerves, the lumbar plexus is formed by the upper four lumbar nerves, and the sacral plexus is made up of the last lumbar and the upper four sacral nerves. [Pg 85]

The only important branch of any of the four upper cervical nerves, which in general supply the neck and shoulders, is the phrenic, which is distributed to the pericardium, the pleuræ, and the under surface of the diaphragm.

The only significant branch of any of the four upper cervical nerves, which generally supply the neck and shoulders, is the phrenic, which goes to the pericardium, the pleurae, and the underside of the diaphragm.

The brachial plexus, as its name implies, supplies the arms and has a number of important branches, as the circumflex to the shoulder, the musculo-cutaneous to the upper arm, the elbow-joint, and the outer surface of the forearm, the internal cutaneous to the inner side of the arm, the median to the pronators and flexors and the fingers on the radial side, and the ulnar to the elbow and wrist-joint. The musculo-spiral runs down the spiral groove to the external condyle of the humerus or upper arm bone, where it divides into the radial and the posterior interosseous, the former going to the thumb and two adjacent fingers and the latter to the wrist-joint and the muscles on the back of the forearm. Sometimes, in fracture of the humerus the callus thrown out pinches the musculo-spiral and causes pain.

The brachial plexus, as its name suggests, supplies the arms and has several key branches, including the circumflex for the shoulder, the musculo-cutaneous for the upper arm, the elbow joint, and the outer surface of the forearm, the internal cutaneous for the inner side of the arm, the median for the pronators, flexors, and fingers on the radial side, and the ulnar for the elbow and wrist joint. The musculo-spiral runs down the spiral groove to the external condyle of the humerus, or upper arm bone, where it splits into the radial and the posterior interosseous. The radial goes to the thumb and two adjacent fingers, while the posterior interosseous goes to the wrist joint and the muscles on the back of the forearm. Sometimes, when the humerus is fractured, the callus that forms can pinch the musculo-spiral, causing pain.

The dorsal or thoracic nerves supply the back with their posterior divisions and their anterior divisions are the intercostal nerves.

The dorsal or thoracic nerves provide the back with their posterior divisions, while their anterior divisions are the intercostal nerves.

The lumbar nerves supply the abdomen, pelvis, and thigh, the chief branches being the ilio-hypogastric to the abdomen and gluteal region, the ilio-inguinal to the inguinal region and scrotum, the external cutaneous and genito-crural to the thigh, and the obturator to the thigh and the hip and knee-joints. The anterior crural descends beneath Poupart’s ligament and divides into an anterior and a posterior division which supply the thigh muscles, its branches going to the pelvis.

The lumbar nerves provide nerve supply to the abdomen, pelvis, and thigh. The main branches include the ilio-hypogastric nerve for the abdomen and gluteal area, the ilio-inguinal nerve for the inguinal area and scrotum, the external cutaneous and genito-crural nerves for the thigh, and the obturator nerve for the thigh as well as the hip and knee joints. The anterior crural nerve runs underneath Poupart’s ligament and splits into an anterior and a posterior division, which serve the thigh muscles, with branches extending to the pelvis.

Fig. 30.—Diagrammatic view of the sympathetic cord of the right side, showing its connections with the principal cerebro-spinal nerves and the main preaortic plexuses. (Reduced from Quain’s anatomy.)

Fig. 30.—Diagram of the sympathetic cord on the right side, illustrating its connections with the major cerebro-spinal nerves and the main preaortic plexuses. (Reduced from Quain’s anatomy.)

The sacral plexus supplies the organs of the pelvis, the thigh, and the leg. Its chief branches are the great sciatic, the largest nerve in the body, and the small sciatic, which go to the buttocks and thigh. The great sciatic runs down the back of the thigh and divides at the [Pg 86] lower third of the thigh into the internal and external popliteal nerves, the former of which passes along the back of the thigh to the knee, where it becomes the posterior tibial, which in turn divides at the ankle into the internal and external plantar. The external popliteal [Pg 87] descends along the outer side of the popliteal space and divides an inch below the head of the fibula into the anterior tibial, which supplies the flexors and skin of the ankle-joint, and the musculo-cutaneous, which sends branches to the skin of the lower leg and the dorsum of the foot.

The sacral plexus supplies the organs in the pelvis, thigh, and leg. Its main branches are the great sciatic, the largest nerve in the body, and the small sciatic, which go to the buttocks and thigh. The great sciatic runs down the back of the thigh and splits at the [Pg 86] lower third of the thigh into the internal and external popliteal nerves. The internal popliteal nerve travels along the back of the thigh to the knee, where it becomes the posterior tibial nerve. This nerve then divides at the ankle into the internal and external plantar nerves. The external popliteal nerve [Pg 87] descends along the outer side of the popliteal space and splits an inch below the head of the fibula into the anterior tibial nerve, which supplies the flexors and skin of the ankle joint, and the musculo-cutaneous nerve, which sends branches to the skin of the lower leg and the top of the foot.

The Sympathetic System.—Joined to the cerebro-spinal system by intervening cords is the sympathetic system. This is made up of two series of ganglia, one on either side of the spinal column, connected by longitudinal bands and extending from the base of the skull to the coccyx. They do not form an independent nervous system, each ganglion, which seems to resemble the motor cells of the spinal cord, being connected by motor and sensory fibers with the cerebral system.

The Sympathetic System.—Connected to the cerebro-spinal system by intervening cords is the sympathetic system. This system consists of two series of ganglia, one on each side of the spinal column, linked by longitudinal bands and stretching from the base of the skull to the coccyx. They do not create an independent nervous system; each ganglion, which looks similar to the motor cells of the spinal cord, is connected by motor and sensory fibers to the cerebral system.

The sympathetic nerves are mostly gray, non-medullated fibers and are distributed to viscera, secreting glands, and blood-vessels, whose movements are involuntary and feelings obtuse. They form networks upon the heart and other viscera and send branches to the cranium to the organs of special sense. There are three main plexuses: The solar plexus behind the stomach, which supplies the abdominal viscera; the hypogastric plexus in front of the prominence of the sacrum, whose nerves go to the pelvic organs; and the cardiac plexus behind the aortic arch for the thoracic viscera.

The sympathetic nerves are mostly gray, unmyelinated fibers that are distributed to the organs, glands, and blood vessels, whose movements are involuntary and sensations are dull. They create networks on the heart and other organs and send branches to the brain for the special sensory organs. There are three main plexuses: The solar plexus behind the stomach, which supplies the abdominal organs; the hypogastric plexus in front of the sacrum, with nerves that go to the pelvic organs; and the cardiac plexus behind the aortic arch for the thoracic organs.

Over these nerves one has no control. A blow in the region between the costal cartilages and below the sternum is a solar plexus blow and is very upsetting.

Over these nerves, you have no control. A hit in the area between the rib cartilages and below the breastbone is a solar plexus hit and is very distressing.

The sympathetic system serves to maintain vitality in all the important portions of the system and one of its important functions is to keep up communication between one part and another, so that when any organ is affected the others will act accordingly and help out to the best of their ability.

The sympathetic system helps keep everything running smoothly in all the important parts of the body. One of its key roles is to ensure communication between different parts, so that when one organ is impacted, the others respond appropriately and provide assistance as best as they can.


CHAPTER VI.
THE BACK.

Fig. 31.
The spinal column.
(Church and Peterson.)

Fig. 31.
The spine.
(Church and Peterson.)

The Spine.—The trunk may be roughly divided into the back, the chest or thorax, the abdomen, and the pelvis. By the back is denoted the spinal column with its muscles, blood-vessels, etc., and the spinal cord already described. The spine or vertebral column, which serves the double purpose of holding the body erect and of protecting the cord, is usually about two feet, two inches in length. In its course there occur several curves, which serve to give springiness and strength and, with the intervertebral cartilages, to mitigate the force of concussion from blows and falls. The curve is convex forward in the cervical region, convex backward in the dorsal, forward in the lumbar, and backward again in the sacral region. There is most freedom of motion in the cervical region.

The Spine.—The trunk can be roughly divided into the back, the chest or thorax, the abdomen, and the pelvis. The back refers to the spinal column along with its muscles, blood vessels, etc., and the spinal cord previously described. The spine or vertebral column serves two main purposes: it keeps the body upright and protects the spinal cord. It is typically about two feet, two inches long. Along its length, there are several curves that provide flexibility and strength, and along with the intervertebral cartilages, help absorb the impact from hits and falls. The curve is rounded forward in the cervical area, rounded backward in the dorsal region, forward again in the lumbar section, and backward once more in the sacral area. The cervical region allows for the most movement.

As is the case with the other bones, the vertebræ are specially adapted in shape and size to the needs they are called upon to fill. Strength and flexibility, with a minimum bulk, a channel for the cord, and passages for the numerous nerves and blood-vessels are some of the requirements which, in combination, they meet to an astonishing degree. They are thirty-three in all, and are divided into groups according to the region in which they occur: seven cervical in the neck, twelve dorsal or thoracic, five lumbar, five sacral, and four coccygeal. [Pg 89]

Like the other bones, the vertebrae are specifically shaped and sized to meet the functions they serve. They provide strength and flexibility with minimal bulk, create a channel for the spinal cord, and have passages for many nerves and blood vessels—requirements they fulfill to an impressive extent. There are a total of thirty-three vertebrae, which are grouped by the area in which they are located: seven cervical in the neck, twelve dorsal or thoracic, five lumbar, five sacral, and four coccygeal. [Pg 89]

Although the vertebræ of the different groups differ more or less in size and shape in accordance with the various demands of their positions, they all have certain general characteristics. Each has a body, two laminæ, two pedicles, two transverse processes, and one spinous process. The pedicles extend back from the body on either side and support two broad plates of bone, the laminæ, whose juncture at the back completes the spinal foramen for the passage of the cord. At their juncture is the spinous process, which can be felt beneath the skin, while the transverse processes project from the juncture of the laminæ with the pedicles. All the processes are for the attachment of muscles that move the spine. The body is formed of cancellous bone with a compact layer outside. Transversely it is slightly oval, while its upper and lower surfaces are flat, except in the cervical region, where the upper surface is concave laterally and the under convex laterally and concave from before back. Between the bodies are disks of fibro-cartilage, which increases motion and springiness. The spinous process or spine is short in the cervical region, long and directed downward in the dorsal region, thick and projecting almost straight out in the lumbar region. The pedicles are notched above and below so that [Pg 90] when articulated the notches of two vertebræ join to form the intervertebral foramen for the outward passage of nerves and the inward passage of blood-vessels.

Although the vertebrae of different groups vary in size and shape based on their positions, they all share certain common features. Each has a body, two laminae, two pedicles, two transverse processes, and one spinous process. The pedicles extend backward from the body on each side and support two broad plates of bone, the laminae, whose meeting at the back completes the spinal foramen for the passage of the spinal cord. At their meeting point is the spinous process, which can be felt under the skin, while the transverse processes extend from where the laminae connect to the pedicles. All the processes are for attaching muscles that move the spine. The body is made of cancellous bone with a compact outer layer. Transversely, it is slightly oval, with flat upper and lower surfaces, except in the cervical region where the upper surface is concave on the sides and the lower is convex on the sides and concave from front to back. Between the bodies are disks of fibro-cartilage that enhance movement and provide springiness. The spinous process or spine is short in the cervical region, long and directed downward in the dorsal region, and thick and projecting almost straight out in the lumbar region. The pedicles have notches above and below so that [Pg 90] when articulated, the notches of two vertebrae come together to form the intervertebral foramen for the outward passage of nerves and the inward passage of blood vessels.

The distinguishing mark of the cervical vertebræ is the foramen in each transverse process, through which the vertebral arteries run to the skull. They are also smaller than the dorsal and lumbar vertebræ. The dorsal vertebræ are distinguished by having on the transverse processes and on the body smooth articular surfaces called facets and demi-facets for articulation with the ribs. The lumbar vertebræ are the largest and heaviest and have the thickest spine. By the time the sacral region is reached, however, the vertebræ have only a rudimentary spinous process. Moreover, in adult age the sacral bones grow together and form one triangular bone, the sacrum, which has a broad base called the promontory of the sacrum and a blunt apex. It is concave in front and convex behind and has an articulating surface for joining the pelvic bones. In the case of the coccyx also the four original bones, all rudimentary in character and supposed to be the survival of a tail, grow together to form one bone. Together the sacrum and coccyx form the posterior wall of the true pelvis.

The main feature of the cervical vertebrae is the foramen in each transverse process, which allows the vertebral arteries to travel to the skull. They are also smaller than the dorsal and lumbar vertebrae. The dorsal vertebrae are identified by having smooth articular surfaces known as facets and demi-facets on the transverse processes and on the body, which articulate with the ribs. The lumbar vertebrae are the largest and heaviest, with the thickest spine. However, by the time the sacral region is reached, the vertebrae only have a rudimentary spinous process. Moreover, in adulthood, the sacral bones fuse together to form one triangular bone, the sacrum, which has a broad base called the promontory of the sacrum and a blunt apex. It is concave in the front and convex in the back and has a surface for connecting with the pelvic bones. The coccyx also consists of four original bones, all rudimentary and thought to be remnants of a tail, that fuse into one bone. Together, the sacrum and coccyx make up the back wall of the true pelvis.

Fig. 32.—A type of vertebra. (Leidy.) 1, Body; 2, pedicle; 3, lamina; 4, spinal foramen; 5, spinous process; 6, transverse process; 7, articular process.

Fig. 32.—A type of vertebra. (Leidy.) 1, Body; 2, pedicle; 3, lamina; 4, spinal foramen; 5, spinous process; 6, transverse process; 7, articular process.

Fig. 33.—The sacrum, from before.
(Drawn by D. Gunn.)

Fig. 33.—The sacrum, from the front.
(Illustration by D. Gunn.)

[Pg 91] Some of the dorsal vertebræ are peculiar in the arrangement of their facets and demi-facets, while among the cervical vertebræ are several whose peculiarities should be more carefully noted. Thus, the first cervical vertebra or atlas supports the head and has practically no body, the place of the body being taken by a narrow anterior arch of bone and an opening, continuous with the spinal foramen, into which the odontoid process of the axis fits, being held in place by ligaments. At either side on top is a facet for articulation with the occipital bone. There is almost no spine. The second vertebra or axis has surmounting the body the odontoid process, with a facet in front for articulation with the atlas and one behind for the transverse ligament to move over. The seventh cervical vertebra or vertebra prominens has a very long spinous process—hence name—to which is attached the ligamentum nuchæ. It can be felt very distinctly on the living.

[Pg 91] Some of the dorsal vertebrae have a unique arrangement of their facets and demi-facets, while there are several cervical vertebrae with notable characteristics that deserve more attention. For instance, the first cervical vertebra, or atlas, supports the head and has almost no body; instead, a narrow anterior arch of bone takes the place of the body, along with an opening that connects to the spinal foramen, where the odontoid process of the axis fits securely, held in place by ligaments. On either side at the top, there's a facet for connecting with the occipital bone. There’s almost no spine. The second vertebra, or axis, has the odontoid process rising from the body, with a facet in front for its connection to the atlas and one behind for the transverse ligament to slide over. The seventh cervical vertebra, or vertebra prominens, features a very long spinous process, which gives it its name, and to which the ligamentum nuchae is attached. This can be felt very clearly on a living person.

Running from the skull down through the spinal column into the sacral vertebræ and formed by the joining of the spinal foramina of the individual vertebræ is an opening called the spinal canal, which holds the cord. The cord, however, stops practically at the first lumbar vertebra, where it splits up into the cauda equina, only the filum terminate extending farther down.

Running from the skull down through the spinal column into the sacral vertebrae and formed by the joining of the spinal foramina of the individual vertebrae is an opening called the spinal canal, which holds the cord. The cord, however, stops almost at the first lumbar vertebra, where it splits into the cauda equina; only the filum terminate extends further down.

Occasionally the laminæ do not form completely and the membranes of the cord may bulge out and form a tumor, or the cord itself may come out also. This generally occurs in the lumbar region, where it is known as spina bifida. If in case of fracture of a vertebra there is paralysis of the parts below due simply to the pressure of a fragment of bone upon the cord, it may be completely cured by removal of the fragment. If, however, the cord suffers injury, the paralysis will remain. Humpback or Pott’s disease is caused by the tubercle bacillus, which eats away the bodies of the vertebræ so that the column caves in and the spinous processes are thrown out in a hump or kyphos. [Pg 92]

Sometimes the laminæ don’t form completely, causing the membranes of the cord to bulge out and form a tumor, or the cord itself may protrude as well. This usually happens in the lumbar region and is known as spina bifida. If a vertebra is fractured and causes paralysis below due to pressure from a bone fragment on the cord, it can often be completely cured by removing the fragment. However, if the cord is injured, the paralysis will persist. Humpback or Pott’s disease is caused by the tubercle bacillus, which destroys the vertebral bodies, leading to a collapse of the column and the spinous processes protruding in a hump or kyphosis. [Pg 92]

Fig. 34.—Muscles of the right side of the head and neck: 1, Frontalis; 2, superior auricular; 3, posterior auricular; 4, orbicularis palpebrarum; 5, pyramidalis nasi; 6, compressor naris; 7, levator labii superioris alæque nasi; 8, levator labii superioris; 9, zygomaticus major; 10, orbicularis oris; 11, depressor labii inferioris; 12, depressor anguli oris; 13, anterior belly of digastric; 14, mylohyoid; 15, hyoglossus; 16, stylohyoid; 17, posterior belly of digastric; 18, the masseter; 19, sternohyoid; 20, anterior belly of omohyoid; 21, thyrohyoid; 22, 23, lower and middle constrictors of pharynx; 24, sternomastoid; 25, 26, splenius; 27, levator scapulæ; 28, anterior scalenus; 29, posterior belly of omohyoid; 30, middle and posterior scalenus; 31, trapezius. (Dorland’s Dictionary.)

Fig. 34.—Muscles of the right side of the head and neck: 1, Frontalis; 2, superior auricular; 3, posterior auricular; 4, orbicularis palpebrarum; 5, pyramidalis nasi; 6, compressor naris; 7, levator labii superioris alæque nasi; 8, levator labii superioris; 9, zygomaticus major; 10, orbicularis oris; 11, depressor labii inferioris; 12, depressor anguli oris; 13, anterior belly of digastric; 14, mylohyoid; 15, hyoglossus; 16, stylohyoid; 17, posterior belly of digastric; 18, masseter; 19, sternohyoid; 20, anterior belly of omohyoid; 21, thyrohyoid; 22, 23, lower and middle constrictors of pharynx; 24, sternocleidomastoid; 25, 26, splenius; 27, levator scapulae; 28, anterior scalene; 29, posterior belly of omohyoid; 30, middle and posterior scalene; 31, trapezius. (Dorland’s Dictionary.)

Muscles of the Neck.—Before speaking of the muscles of the back a few of those of the neck had best be taken up. They are numerous but mostly of minor importance. Largest and most important is the sterno-cleido-mastoid muscle, which has its origin on the upper part of the sternum and the inner third of the clavicle and is inserted into the mastoid process of the temporal bone. It passes obliquely across the side of the neck and serves to flex the head to the side and to draw the face in the opposite direction. When both muscles contract the head is flexed on the neck and the neck on the chest. In wry neck or torticollis this muscle is constantly contracted. The platysma myoides arises from the fascia over the pectoral, deltoid, and trapezius muscles and is inserted into the lower jaw, the angle of the mouth, and the loose tissue in the lower part of the face. It [Pg 93] wrinkles the skin of the neck and depresses the lower jaw. In the cow and horse it is so highly developed that by it the skin can be contracted all over the body to drive off flies. The rectus capitis anticus major arises from the third to the sixth cervical vertebræ and is inserted into the occipital bone, serving to flex the head. The scalenus muscles have their origin on the lower cervical vertebræ and are inserted into the first and second ribs, thus aiding in the elevation of the ribs as well as in lateral flexion of the neck. The head is held upright by the ligamentum nuchæ, which rises from the external occipital protuberance and is inserted into the spinous processes of all the cervical vertebræ except the first.

Muscles of the Neck.—Before discussing the muscles of the back, it's important to cover a few of those in the neck. There are many, but most are not very significant. The largest and most important is the sternocleidomastoid muscle, which originates from the upper part of the sternum and the inner third of the clavicle and inserts into the mastoid process of the temporal bone. It runs diagonally across the side of the neck and helps flex the head to the side while turning the face in the opposite direction. When both muscles contract, the head flexes on the neck and the neck flexes on the chest. In cases of wry neck or torticollis, this muscle is constantly contracted. The platysma myoides comes from the fascia over the pectoral, deltoid, and trapezius muscles and inserts into the lower jaw, the corners of the mouth, and the loose tissue in the lower part of the face. It wrinkles the skin of the neck and lowers the jaw. In cows and horses, it is so well-developed that it can contract the skin all over the body to shoo away flies. The rectus capitis anticus major originates from the third to the sixth cervical vertebrae and attaches to the occipital bone, helping to flex the head. The scalenus muscles originate on the lower cervical vertebrae and insert into the first and second ribs, aiding in rib elevation and lateral neck flexion. The head is kept upright by the ligamentum nuchae, which extends from the external occipital protuberance and attaches to the spinous processes of all the cervical vertebrae, except for the first.

Muscles of the Back.—The chief back muscles are the trapezius and the latissimus dorsi, which together cover in the back pretty thoroughly. The trapezius arises from the occipital bone, the ligamentum nuchæ, and the spinous processes of the seventh cervical and all the dorsal vertebræ and is inserted into the outer third of the clavicle or collar bone and the acromion process and spine of the scapula or shoulder blade. It is thus triangular in shape and covers in the neck and shoulders, serving to draw the head back and to the side. It overlaps the latissimus dorsi.

Muscles of the Back.—The main back muscles are the trapezius and the latissimus dorsi, which together provide extensive coverage of the back. The trapezius originates from the occipital bone, the ligamentum nuchae, and the spinous processes of the seventh cervical and all the thoracic vertebrae, and it attaches to the outer third of the clavicle (collarbone) and the acromion process and spine of the scapula (shoulder blade). It's shaped like a triangle and spans the neck and shoulders, helping to pull the head back and to the side. It overlaps the latissimus dorsi.

The latissimus dorsi has its origin by aponeurosis from the spinous processes of the six lower dorsal and all the lumbar and sacral vertebræ, from the crest of the ilium or hip bone, and from the three or four lower ribs, swings across the side, dwindling in size, and is inserted by a small tendon into the bicipital groove of the humerus or upper arm bone, thus covering in the part of the back not covered by the trapezius. It draws the arm down and back, raises the lower ribs, and draws the trunk forward, as in climbing. The flat muscles of the back and abdomen have a tendency to flatten out into aponeuroses, such as occurs in the origin of the latissimus dorsi.

The latissimus dorsi originates from the aponeurosis of the spinous processes of the six lower thoracic vertebrae and all the lumbar and sacral vertebrae, from the crest of the ilium (hip bone), and from the three or four lower ribs. It travels across the side, decreasing in size, and attaches by a small tendon to the bicipital groove of the humerus (upper arm bone), covering the back part that isn’t covered by the trapezius. It pulls the arm downward and backward, lifts the lower ribs, and moves the trunk forward, like when climbing. The flat muscles of the back and abdomen tend to spread into aponeuroses, which is what happens at the origin of the latissimus dorsi.

The levator scapulæ, from the transverse processes of the upper [Pg 94] cervical vertebræ to the posterior border of the scapula, serves to raise the angle of the scapula, and the rhomboideus major and minor, from the ligamentum nuchæ, the seventh cervical, and the upper dorsal vertebræ to the root of the spine of the scapula, draw the inferior angle back and up.

The levator scapulæ, from the transverse processes of the upper [Pg 94] cervical vertebrae to the back edge of the shoulder blade, helps lift the angle of the shoulder blade, and the rhomboideus major and minor, from the nuchal ligament, the seventh cervical, and the upper thoracic vertebrae to the base of the spine of the shoulder blade, pull the bottom angle back and upward.

Fig. 35.—Muscles of the trunk from behind (left side, superficial; right side, deep): 1, Sternomastoid; 2, splenius; 3, trapezius; 4, latissimus dorsi; 5, infraspinatus; 6, teres minor; 7, teres major; 8, deltoid; 9, external oblique of abdomen; 10, gluteus medius; 11, gluteus maximus; 12, levator anguliscapulæ; 13, rhomboideus minor; 14, rhomboideus major; 15, part of longissimus dorsi; 16, tendons of insertion of iliocostalis; 17, supraspinatus; 18, infraspinatus; 19, teres minor; 20, teres major; 21, serratus magnus; 22, upper, and 22´, lower part of serratus posticus inferior; 23, internal oblique; 24, gluteus medius; 25, pyriformis and superior and inferior gemelli; 26, 26´, portions of obturator internus; 27, tendon of obturator internus; 28, quadratus femoris. (Dorland’s Dictionary.)

Fig. 35.—Muscles of the trunk from behind (left side, superficial; right side, deep): 1, Sternomastoid; 2, splenius; 3, trapezius; 4, latissimus dorsi; 5, infraspinatus; 6, teres minor; 7, teres major; 8, deltoid; 9, external oblique of abdomen; 10, gluteus medius; 11, gluteus maximus; 12, levator anguliscapulæ; 13, rhomboideus minor; 14, rhomboideus major; 15, part of longissimus dorsi; 16, tendons of insertion of iliocostalis; 17, supraspinatus; 18, infraspinatus; 19, teres minor; 20, teres major; 21, serratus magnus; 22, upper, and 22´, lower part of serratus posticus inferior; 23, internal oblique; 24, gluteus medius; 25, pyriformis and superior and inferior gemelli; 26, 26´, portions of obturator internus; 27, tendon of obturator internus; 28, quadratus femoris. (Dorland’s Dictionary.)

The blood supply in the cervical region and about the shoulders comes from branches of the subclavian artery, such as the suprascapular and [Pg 95] the transversalis colli. Lower down the supply comes from the posterior branches of the intercostals, dorsal branches of the lumbar, and branches of the internal iliac.

The blood supply in the neck area and around the shoulders comes from branches of the subclavian artery, like the suprascapular and the transversalis colli. Further down, the supply comes from the posterior branches of the intercostals, dorsal branches of the lumbar, and branches of the internal iliac.

The muscles of the back are supplied by the spinal nerves, the spinal accessory also going to the trapezius muscle.

The muscles in the back are supplied by the spinal nerves, with the spinal accessory also connecting to the trapezius muscle.


CHAPTER VII.
THE CHEST.

The chest or thorax occupies the upper part of the trunk in front and is a dome-shaped cavity containing and protecting the heart and lungs. Its walls are formed by the dorsal vertebræ at the back, the ribs at either side, and the sternum and costal cartilages in front, all well covered with muscles. The floor is formed by the diaphragm. Through the upper opening of the chest pass the trachea, the esophagus, and many important vessels and nerves.

The chest, or thorax, is the upper part of the trunk at the front and is a dome-shaped space that holds and protects the heart and lungs. Its walls are made up of the back vertebrae, the ribs on either side, and the sternum and costal cartilages in front, all well covered with muscles. The floor is made by the diaphragm. The upper opening of the chest lets the trachea, esophagus, and many important blood vessels and nerves pass through.

Fig. 36.—Thorax (anterior view.)
(Ingals.)

Fig. 36.—Chest (front view.)
(Ingals.)

[Pg 97] The shape of the chest may vary in disease. Thus, in rickets there is the prominent “pigeon” breast and the rosary, that is, a bead at the juncture of each rib with the costal cartilage, while in emphysema the chest is enlarged in all directions and barrel-shaped. In severe cases of lateral curvature it is distorted but may be improved by exercises.

[Pg 97] The shape of the chest can change due to illness. For example, in rickets, there's a noticeable "pigeon" chest and a rosary effect, which means a bump at the point where each rib connects to the costal cartilage. In emphysema, the chest expands in all directions, taking on a barrel shape. In severe cases of scoliosis, the chest can be distorted, but it may improve with exercise.

The Sternum.—The sternum or breast-bone is a long narrow bone and has three parts, the manubrium or handle above, the gladiolus or sword, and the ensiform cartilage at the lower end. On either side are notches for the costal cartilages; for the first seven ribs as well as the clavicle articulate with it. Except for some muscles along the edges it lies directly under the skin and the ridge between the manubrium and the gladiolus can be felt in the living, a fact which assists in determining the position of the different ribs in cases of fracture, as the second rib articulates at this point.

The Sternum.—The sternum, or breastbone, is a long, narrow bone made up of three parts: the manubrium or handle at the top, the gladiolus or sword in the middle, and the ensiform cartilage at the bottom. On either side, there are notches for the costal cartilages; the first seven ribs and the clavicle connect to it. Except for some muscles along the edges, it lies directly under the skin, and the ridge between the manubrium and the gladiolus can be felt in a living person, which helps in locating the different ribs in cases of fractures, as the second rib connects at this point.

Fig. 37.—A and B, typical ribs; C, first rib; D, twelfth rib. 1, head; 2, neck; 3, tuberosity; 4, grooved edge; 5, shaft; 6, oval depression for costa cartilage.

Fig. 37.—A and B, typical ribs; C, first rib; D, twelfth rib. 1, head; 2, neck; 3, tuberosity; 4, grooved edge; 5, shaft; 6, oval depression for costal cartilage.

The Ribs.—The ribs are twenty-four in number, twelve on each side, of which the upper seven, which articulate with the sternum by individual cartilages, are called true ribs, the other five false ribs. Of the false ribs the upper three articulate indirectly with the sternum through the seventh cartilage, with which their cartilages unite, while the other two have their anterior extremities free and are [Pg 98] called floating ribs. All the ribs slope down toward the front and are by nature more freely movable in women than in men. Most of the ribs have a head divided by a little ridge into two facets for articulation with the dorsal vertebræ, a flattened neck, a tuberosity at the base of the neck with a facet for articulation with the transverse process of the vertebra below, an angle, and a shaft, which is externally convex and is grooved on its lower edge for the intercostal vessels and nerve. The first and second, eleventh and twelfth ribs, however, are somewhat peculiar, the first two being shorter, flatter and rather broader than the rest and the first having only one facet on the head, while the last two have only one facet on the head and no neck or tuberosity.

The Ribs.—There are twenty-four ribs in total, twelve on each side, with the upper seven connecting to the sternum via individual cartilages, known as true ribs. The remaining five are called false ribs. Of the false ribs, the upper three connect to the sternum indirectly through the seventh cartilage, which their cartilages join, while the last two have free anterior ends and are referred to as floating ribs. All ribs slope downward toward the front and are generally more flexible in women than in men. Most ribs have a head divided by a little ridge with two facets for connecting to the dorsal vertebrae, a flattened neck, a tuberosity at the base of the neck for connecting to the transverse process of the vertebra below, an angle, and a shaft that is curved outward and grooved on its lower edge for the intercostal vessels and nerves. However, the first, second, eleventh, and twelfth ribs are a bit different; the first two are shorter, flatter, and wider than the others, with the first rib having only one facet on its head, while the last two also have just one facet on their head and lack a neck or tuberosity.

The costal cartilages serve to prolong the ribs and greatly increase the elasticity of the chest wall. They grow longer down to the seventh and then decrease again in length.

The costal cartilages help extend the ribs and significantly enhance the flexibility of the chest wall. They grow longer until the seventh rib and then decrease in length again.

The ribs, except the first and second, which are protected by the clavicle, are frequently broken. Such a break causes pain in breathing and sometimes the end of a rib pierces the lung tissue and swelling all over the body results, due to the presence of air. Caries or death of the rib is also frequent. Fracture of the sternum occurs occasionally, generally from direct force, as from a blow with the knee in foot-ball, and there may be dislocation between the manubrium and gladiolus.

The ribs, except for the first and second ones, which are protected by the collarbone, are often broken. Such a break leads to pain when breathing, and sometimes the end of a rib can puncture the lung tissue, causing swelling throughout the body due to air escaping. Bone decay or death of the rib is also common. Sternal fractures happen occasionally, usually from direct impact, like a knee to the chest in football, and there may be dislocation between the manubrium and gladiolus.

Muscles of the Chest.—The spaces between the ribs, from the tubercle of the rib behind to the cartilage in front, are filled by the external intercostal muscles, which pass downward and forward from the lower border of one rib to the upper border of the one below. There are, therefore, eleven pairs of these muscles. There are also eleven pairs of the internal intercostals, which commence at the sternum and extend back to the angle of the rib. These extend downward and backward. The external intercostals raise and evert the ribs in inspiration, the internal depress and invert them in expiration. [Pg 99]

Muscles of the Chest.—The spaces between the ribs, from the rib tubercle in the back to the cartilage in the front, are occupied by the external intercostal muscles, which run down and forward from the lower edge of one rib to the upper edge of the rib below it. So, there are a total of eleven pairs of these muscles. There are also eleven pairs of internal intercostals, which start at the sternum and go back to the angle of the rib. These muscles extend down and back. The external intercostals lift and push out the ribs during inhalation, while the internal intercostals lower and pull in the ribs during exhalation. [Pg 99]

The chief respiratory muscle, however, is the diaphragm, a somewhat fan-shaped muscle that forms the floor of the chest cavity. It takes its origin from the ensiform cartilage, the six or seven lower ribs and their cartilages, and from the upper three or four lumbar vertebræ, that is, from the whole of the internal circumference of the thorax, and is inserted into the central cordiform tendon. It has several large and several small openings for the aorta, the esophagus, the venæ cavæ, the thoracic duct, and various nerves, and its surfaces are covered by serous membranes, by the two pleuræ and the pericardium above and by the peritoneum below. It partially supports the heart and lungs. Convex toward the chest, it becomes flattened in contraction and so increases the capacity of the chest. It aids in all expulsive acts, as sneezing, coughing, laughing, urinating, defecating, vomiting, and childbirth. Hiccough is spasm of the diaphragm.

The main muscle used for breathing is the diaphragm, which is shaped like a fan and forms the bottom of the chest cavity. It starts from the xiphoid process, the six or seven lower ribs and their cartilages, and the upper three or four lumbar vertebrae, covering the entire internal circumference of the thorax, and connects to the central tendon. It has several large and small openings for the aorta, esophagus, venae cavae, thoracic duct, and various nerves, with its surfaces covered by serous membranes, including the two pleurae and the pericardium above and the peritoneum below. It helps support the heart and lungs. Curved towards the chest, it flattens when contracted, which increases the chest's capacity. It assists in all actions that expel air, such as sneezing, coughing, laughing, urinating, defecating, vomiting, and giving birth. Hiccough is a spasm of the diaphragm.

Fig. 38.—Interior view of the diaphragm. (Leidy.) 1-3, The three lobes of the central tendon, surrounded by the fleshy fasciculi derived from the inferior margin of the thorax; 4, 5, the crura; 6, 7, the arcuate ligaments; 8, aortic orifice; 9, esophageal orifice; 10, quadrate foramen; 11, psoas muscle; 12, quadrate lumbar muscle.

Fig. 38.—Interior view of the diaphragm. (Leidy.) 1-3, The three lobes of the central tendon, surrounded by the fleshy bundles coming from the lower edge of the ribcage; 4, 5, the crura; 6, 7, the arcuate ligaments; 8, aortic opening; 9, esophageal opening; 10, quadrate foramen; 11, psoas muscle; 12, quadrate lumbar muscle.

[Pg 100] The arteries of the chest are the intercostal branches of the subclavian and the thoracic aorta, the phrenic, mediastinal, and intercostal branches of the internal mammary, and the thoracic branches of the axillary.

[Pg 100] The arteries in the chest consist of the intercostal branches of the subclavian artery and the thoracic aorta, along with the phrenic, mediastinal, and intercostal branches of the internal mammary artery, as well as the thoracic branches of the axillary artery.

The nerves are the intercostals and phrenics.

The nerves are the intercostals and phrenics.

Mammary Glands.—On the outside of the chest walls, lodged in the fascia of the pectoral muscles, are the mammary glands, accessory organs of the generative system. They exist in both sexes but are only rudimentary in the male. In the female they are small before puberty but enlarge as the generative organs become more completely developed, forming two hemispherical eminences, one on either side, between the third and seventh ribs. During pregnancy they increase once more in size preparatory to the secretion of the milk, and in old age they atrophy. From the middle projects a small pinkish-brown conical eminence, the nipple, surrounded by a paler area, the areola. After the second month of pregnancy both nipple and areola become darker in color, a point of great diagnostic value in early pregnancy.

Mammary Glands.—Located on the outer chest walls, embedded in the fascia of the pectoral muscles, are the mammary glands, which are accessory organs of the reproductive system. They are present in both males and females but are only underdeveloped in men. In females, they are small before puberty but grow as the reproductive organs fully develop, forming two rounded bumps, one on each side, between the third and seventh ribs. During pregnancy, they grow larger again in preparation for milk production, and in older age, they shrink. From the center protrudes a small pinkish-brown cone called the nipple, which is surrounded by a lighter area known as the areola. After the second month of pregnancy, both the nipple and areola darken in color, which is a key diagnostic indicator in early pregnancy.

The mammary glands themselves consist of lobules of gland tissue with a central lactiferous tubule, the lobules being gathered into lobes with fatty tissue between. From the juncture of these tubules result fifteen or twenty excretory ducts, the tubuli lactiferi, which converge toward the areola. Beneath the nipple they dilate, forming the ampullæ, and then contract again to pass out through the nipple as straight tubes.

The mammary glands consist of lobules of glandular tissue with a central lactiferous tubule, and the lobules are grouped into lobes with fatty tissue in between. From the junction of these tubules, about fifteen to twenty excretory ducts, known as the tubuli lactiferi, merge toward the areola. Beneath the nipple, they expand, forming the ampullæ, and then contract again to exit through the nipple as straight tubes.

Breast abscess occurs most commonly in nursing mothers, as where a part is most active there is most danger of abscess. Many benign tumors of the breast, as the fibrous tumors, occur and are especially common in young women. If a fibrous tumor is allowed to develop it may become cancerous. Cancer, however, generally occurs after the age of forty and is usually due to some irritation, as to a blow from a ball.

Breast abscess is most commonly seen in nursing mothers, as areas that are more active have a higher risk of abscesses. Many benign tumors of the breast, such as fibrous tumors, can occur and are particularly common in young women. If a fibrous tumor is allowed to grow, it may turn cancerous. Cancer, however, typically develops after the age of forty and is usually caused by some form of irritation, like a hit from a ball.

The arteries of the breasts are the thoracic branches of the axillary, the intercostal, and the internal mammary.

The arteries of the breasts are the thoracic branches of the axillary, intercostal, and internal mammary arteries.

The nerves are from the thoracic cutaneous.

The nerves are from the thoracic cutaneous.


CHAPTER VIII.
HEART AND CIRCULATION.

The Heart.—Shielded within the chest are, as has been said, the heart and lungs. The heart lies on the left side behind the sternum and the cartilages of the fourth to seventh ribs in a closed, conical, membranous sac, the pericardium, which is attached by its base to the central tendon of the diaphragm, and whose point extends up between the pleuræ of the lungs. This sac has an external fibrous layer and an internal serous layer that is reflected back over the heart itself, [Pg 102] forming a closed sac, within which a thin fluid is secreted that serves to reduce friction during the movements of the heart, the two inner surfaces sliding over each other with every beat.

The Heart.—Protected inside the chest are, as mentioned, the heart and lungs. The heart is located on the left side, behind the breastbone and the cartilages of the fourth to seventh ribs, in a closed, cone-shaped, membranous sac called the pericardium. This sac is attached at its base to the central tendon of the diaphragm, and its point extends up between the pleura of the lungs. The sac consists of an outer fibrous layer and an inner serous layer that folds back over the heart itself, [Pg 102] creating a closed sac. Within this sac, a thin fluid is secreted to reduce friction during the heart's movements, allowing the two inner surfaces to slide over each other with every beat.

Fig. 39.—The heart.
(Stoney.)

Fig. 39.—The heart.
(Stoney.)

Fig. 40.—Left auricle and ventricle, opened and part of their walls removed to show their cavities: 1, Right pulmonary vein cut short; 1´, cavity of left auricle; 3, 3´, thick wall of left ventricle; 4, portion of same with papillary muscle attached; 5, the other papillary muscles; 6, 6´, the segments of the mitral valve; 7, in aorta is placed over the semilunar valves; 8, pulmonary artery; 10, aorta and its branches. (Allen Thomson.)

Fig. 40.—Left atrium and ventricle, opened and part of their walls removed to show their chambers: 1, Right pulmonary vein cut short; 1´, chamber of left atrium; 3, 3´, thick wall of left ventricle; 4, portion of the same with papillary muscle attached; 5, the other papillary muscles; 6, 6´, the segments of the mitral valve; 7, in aorta positioned over the semilunar valves; 8, pulmonary artery; 10, aorta and its branches. (Allen Thomson.)

The heart itself is a hollow conical organ composed of cardiac muscle, a combination of smooth and striated fibers found nowhere else in the body. It lies obliquely, base up, between the lungs, suspended by the great blood-vessels and with the apex directed downward, forward, and to the left, the apex beat being normally felt in the fifth intercostal space, one inch inside and two inches below the left nipple. In size it varies in different people and is generally smaller in women than in [Pg 103] men. On the average it is five inches long, three and a half inches broad, and two inches thick. A man’s heart usually weighs about eleven ounces and that of a woman nine ounces. It never leaks except from disease and such leakage is fatal.

The heart is a hollow, cone-shaped organ made up of cardiac muscle, which is a mix of smooth and striated fibers that aren’t found anywhere else in the body. It sits at an angle with the base facing up, between the lungs, held in place by the large blood vessels, while the point (or apex) points downward, forward, and to the left. You can typically feel the apex beat in the fifth intercostal space, one inch in and two inches below the left nipple. Its size varies among people and is generally smaller in women than in [Pg 103] men. On average, it measures five inches long, three and a half inches wide, and two inches thick. A man's heart typically weighs around eleven ounces, while a woman's heart weighs about nine ounces. It normally doesn’t leak, except in cases of disease, and such leakage is fatal.

The Cavities.—The heart contains four cavities, two auricles above and two ventricles below, with a longitudinal septum between the auricle and ventricle on the right and those on the left. The posterior surface is largely made up of the left ventricle and the anterior of the right ventricle. The right auricle, which receives the blood from the general circulation, has a capacity of about two fluid ounces and is larger than the left, which receives the blood returning from the lungs, though its walls are thinner. Of the ventricles the left is the larger and its walls are about three times as thick as those of the right, for it has to send the blood all over the body. All the cavities are lined with smooth, transparent, serous membrane, the endocardium, which is continuous with the intima of the great vessels.

The Cavities.—The heart has four chambers: two auricles on the top and two ventricles on the bottom, separated by a longitudinal septum between the right atrium and ventricle and their left counterparts. The back surface consists mainly of the left ventricle, while the front is made up of the right ventricle. The right atrium, which collects blood from the overall circulation, holds about two fluid ounces and is larger than the left atrium, which collects blood returning from the lungs, despite having thinner walls. Among the ventricles, the left one is bigger, with walls about three times thicker than those of the right, as it needs to pump blood throughout the entire body. All chambers are lined with a smooth, clear, serous membrane called the endocardium, which connects with the intima of the major blood vessels.

Fig. 41.—Orifices of the heart, seen from above, both the auricles and the great vessels being removed: PA, Pulmonary artery and its semilunar valves; Ao, aorta and its valves; RAV, tricuspid, and LAV, bicuspid valves; mv, segments of mitral valve; lv, segment of tricuspid valve. (Huxley.)

Fig. 41.—Top view of the heart's openings, with both auricles and the major vessels taken out: PA, pulmonary artery and its semilunar valves; Ao, aorta and its valves; RAV, tricuspid valve, and LAV, bicuspid valve; mv, parts of the mitral valve; lv, part of the tricuspid valve. (Huxley.)

The Valves.—The opening from the auricle into the ventricle on either side is guarded on the ventral side by a valve formed of folds of endocardium. The valve on the right side has three flaps or cusps [Pg 104] and is called the tricuspid valve, while that on the left has two flaps, larger and thicker than those of the tricuspid, and is known as the bicuspid or mitral valve. The flaps of either valve are kept from being forced into the auricle in closing by fine tendinous cords, the chordæ tendineæ, which are attached to the columnæ carneæ, muscular bands or columns projecting from the walls of the ventricle, which contract and hold the chordæ tendineæ taut. The opening into the pulmonary artery is from the posterior part of the right ventricle and is guarded by the semilunar or pulmonary valve, while the aortic opening from the left ventricle is guarded by a similar valve, the aortic valve, the most important valve in the body. All these valves are planned primarily to prevent regurgitation of the blood during contraction of the heart muscle. Pressure in the ventricle must exceed that in the arteries before the semilunar valves will open and the blood can be driven out, just as the auriculo-ventricular valves remain closed until the pressure in the auricles exceeds that in the ventricles.

The Valves.—The opening from the atrium into the ventricle on each side is protected on the front side by a valve made up of folds of endocardium. The valve on the right side has three flaps or cusps [Pg 104] and is called the tricuspid valve, while the valve on the left has two flaps that are larger and thicker than those of the tricuspid and is known as the bicuspid or mitral valve. The flaps of both valves are prevented from being pushed into the atrium when closing by fine tendinous cords, the chordæ tendineæ, which are attached to the columnæ carneæ, muscular bands or columns that stick out from the walls of the ventricle, which contract and keep the chordæ tendineæ tight. The opening to the pulmonary artery is located at the back of the right ventricle and is protected by the semilunar or pulmonary valve, while the aortic opening from the left ventricle is guarded by a similar valve, the aortic valve, the most important valve in the body. All these valves are designed primarily to prevent the backflow of blood during the contraction of the heart muscle. The pressure in the ventricle must be greater than that in the arteries before the semilunar valves will open and blood can be pushed out, just as the atrioventricular valves stay closed until the pressure in the atria exceeds that in the ventricles.

The heart beat is caused by the twisting of the heart upon its axis during contraction of the muscle. Normally it beats rhythmically and regularly, whatever a person does, at a rate of about seventy-two contractions to the minute in the adult. To the regular cardiac cycle, as it is called, there are two periods, the systole and the diastole, the former representing the period of contraction of the ventricles, when the blood is sent to the lungs and over the body, and the latter representing the period of rest following the emptying of the ventricles, during which they are refilled. Contraction of the heart occupies one-fifth of the time of one beat, dilatation two-fifths, and the pause two-fifths. There are really two systoles, one of the auricles and one of the ventricles, but they come so close together that they are practically simultaneous so far as sound is concerned, though they can be distinguished by sight. During systole the tricuspid and mitral valves close sharply to prevent regurgitation [Pg 105] into the auricles, while the semilunar valves open to let the blood out. The cardiac cycle is, therefore, as follows:

The heart beat is caused by the twisting of the heart on its axis during the contraction of the muscle. Normally, it beats rhythmically and regularly, no matter what a person is doing, at a rate of about seventy-two beats per minute in adults. In the regular cardiac cycle, there are two phases: systole and diastole. The systole is the phase when the ventricles contract, pumping blood to the lungs and throughout the body, while the diastole is the resting phase after the ventricles empty, during which they refill. The contraction of the heart takes up one-fifth of the time of one beat, while dilation and the pause each take up two-fifths. There are actually two systoles, one for the atria and one for the ventricles, but they occur so closely together that they are practically simultaneous in terms of sound, although they can be seen separately. During systole, the tricuspid and mitral valves close sharply to prevent backflow into the atria, while the semilunar valves open to allow blood to exit. So, the cardiac cycle is as follows:

Fig. 42.—Diagram of the circulation.
(After Kirke.)

Fig. 42.—Diagram of the circulation.
(After Kirke.)

Circulation.—The blood, after it has given off its oxygen and collected carbon dioxide, returns to the heart through two main channels, the superior and inferior venæ cavæ, the former bringing the blood from the upper part of the body, including the head, neck, and arms, and the latter from the lower part below the diaphragm. The two vessels empty along with the coronary sinus, which is guarded by the coronary valve, into the right auricle. At the same time that they empty into this auricle the four pulmonary veins, the only veins that carry arterial or oxygenated blood, are emptying the fresh blood [Pg 106] from the lungs into the left auricle. When both auricles are full, they contract and send the blood into the ventricles, the auricular systole. As the blood comes through into the ventricles it probably comes around by the walls and closes the auriculo-ventricular valves, though just how the valves close is not certain. When the two ventricles are full they in turn contract, the ventricular systole, and the blood is forced out, that in the right ventricle passing to the lungs for its new supply of oxygen through the pulmonary artery, the only artery to carry venous blood, and that from the left ventricle entering the aorta for general distribution through the body. Following the systole is a pause, the diastole, while the heart fills again.

Circulation.—After the blood releases its oxygen and picks up carbon dioxide, it returns to the heart through two main pathways: the superior and inferior venæ cavæ. The superior vein brings blood from the upper body, including the head, neck, and arms, while the inferior vein brings blood from the lower body below the diaphragm. Both veins empty into the right atrium alongside the coronary sinus, which is protected by the coronary valve. At the same time that these veins empty into the atrium, the four pulmonary veins, the only veins that carry arterial or oxygenated blood, are draining fresh blood from the lungs into the left atrium. When both atria are full, they contract and push blood into the ventricles, known as auricular systole. As the blood flows into the ventricles, it likely moves around the walls and closes the atrioventricular valves, although the exact mechanism of valve closure is uncertain. When both ventricles are full, they contract in turn, during ventricular systole, forcing blood out; the right ventricle sends blood to the lungs for a new supply of oxygen through the pulmonary artery, the only artery carrying venous blood, while blood from the left ventricle enters the aorta for distribution throughout the body. After the systole, there's a pause for diastole, during which the heart fills again.

Fig. 43.—The fetal circulation.

Fig. 43.—Fetal circulation.

Circulation in Fetus.—In the fetus there is direct communication between the two auricles through the foramen ovale, which normally closes at birth, though occasionally it remains open. There is also communication between the pulmonary artery and the arch of the aorta through the ductus arteriosus. The freshly oxidized blood comes to the fetus through the placenta, from which it is brought along the umbilical cord in the umbilical vein to the liver and thence to the inferior vena cava, where it mixes with the blood from the lower extremities. By the inferior vena cava it is carried to the right auricle, where the Eustachian valve—a valve between the inferior vena cava and the auriculo-ventricular opening, larger in the fetus than in later life where it serves no special purpose—guides it across the auricle and through the foramen ovale to the left auricle. From this auricle, together with a small amount of blood from the lungs, it goes to the left ventricle and is distributed by the aorta almost [Pg 107] entirely to the head and upper extremities. Hence their large size and perfect development at birth. Returned from the upper extremities by the superior vena cava, the blood enters the right auricle again and, passing over the Eustachian valve this time, descends to the right ventricle, from which the greater part passes by the pulmonary artery and the ductus arteriosus to the descending aorta, though a small amount keeps on through the pulmonary artery to the lungs. In the aorta it mixes with the blood from the left ventricle and part goes to supply the lower extremities, though the greater part is carried back to the placenta through the two umbilical arteries. The fact that the greater part of the blood traverses the liver accounts for its large size at birth, while the lower extremities, which receive for the most part blood that has already circulated through the upper extremities, are of small size and imperfectly developed.

Circulation in Fetus.—In the fetus, there is direct communication between the two auricles through the foramen ovale, which normally closes at birth, though sometimes it stays open. There's also a connection between the pulmonary artery and the arch of the aorta through the ductus arteriosus. Freshly oxygenated blood reaches the fetus through the placenta, which sends it via the umbilical cord in the umbilical vein to the liver and then to the inferior vena cava, where it mixes with blood from the lower body. From the inferior vena cava, it travels to the right atrium, where the Eustachian valve—a valve between the inferior vena cava and the atrioventricular opening, larger in the fetus than later in life when it has no significant function—guides it across the atrium and through the foramen ovale to the left atrium. From there, along with a small amount of blood from the lungs, it moves to the left ventricle and is pumped by the aorta mainly to the head and upper body. This is why they are large and fully developed at birth. The blood returns from the upper body via the superior vena cava, enters the right atrium again, and after passing over the Eustachian valve this time, goes down to the right ventricle. Most of it then goes through the pulmonary artery and the ductus arteriosus to the descending aorta, although a small portion continues through the pulmonary artery to the lungs. In the aorta, it mixes with blood from the left ventricle, with some directed to the lower extremities, but most returning to the placenta through two umbilical arteries. The fact that most of the blood passes through the liver explains its large size at birth, while the lower extremities, which mostly receive blood that has already circulated through the upper body, are smaller and less developed.

Arteries.—After birth the arterial blood for the general circulation leaves the heart by the aorta, the main distributing artery of the body. Through this and its branches it is carried throughout the body in what, with the return of the venous blood by the venæ cavæ and other smaller veins, is known as the systemic circulation. The aorta ascends from the left ventricle and arches backward to the left over the root of the left lung to descend along the spinal column at the left to the fourth lumbar vertebra, about opposite the umbilicus, where, considerably diminished in size by the branches it has given off, it divides into the two common iliacs. For convenience its different parts are named, according to their position, the ascending aorta, the arch of the aorta, and the descending aorta, the last being subdivided into the thoracic and the abdominal aorta.

Arteries.—After birth, the arterial blood for the general circulation exits the heart through the aorta, the primary artery that distributes blood throughout the body. This blood, along with the returning venous blood via the venae cavae and other smaller veins, is part of what’s known as the systemic circulation. The aorta rises from the left ventricle and arches backward to the left over the root of the left lung, then descends parallel to the spine on the left side to the fourth lumbar vertebra, which is roughly at the level of the belly button. At this point, having reduced in size due to the branches it has given off, it splits into the two common iliacs. For easier reference, its sections are named based on their location: the ascending aorta, the arch of the aorta, and the descending aorta, with the latter further divided into the thoracic and the abdominal aorta.

Fig. 44.—The aortæ and their branches.
(Leidy.)

Fig. 44.—The aorta and its branches.
(Leidy.)

From the ascending aorta come off the coronary arteries which supply the heart muscle itself, as the coronary sinuses carry off the venous blood from the heart. From the arch are given off the left common [Pg 108] carotid and left subclavian and the innominate, which divides into the right common carotid and right subclavian.

From the ascending aorta come the coronary arteries that supply the heart muscle, while the coronary sinuses collect the venous blood from the heart. From the arch, the left common carotid, left subclavian, and innominate arteries branch off, with the innominate splitting into the right common carotid and right subclavian.

The common carotids pass up the neck behind the sterno-cleido-mastoid muscles in a line from the sterno-clavicular joint to a point midway between the mastoid process and the angle of the lower jaw and divide opposite the upper border of the thyroid cartilage into the internal and external carotids, of which the former with its branches supplies the anterior part of the brain, the eye and forehead, and the latter the neck and face.

The common carotid arteries run up the neck behind the sternocleidomastoid muscles in a path from the sternoclavicular joint to a point halfway between the mastoid process and the angle of the lower jaw. They split opposite the upper edge of the thyroid cartilage into the internal and external carotid arteries, with the internal supplying the front part of the brain, the eye, and forehead, while the external supplies the neck and face.

The subclavian is the artery of the upper extremity but its vertebral branch goes to the brain, where with its fellow it forms the basilar artery, whose branches together with the branches of the internal carotid form the circle of Willis at the base of the brain. Other branches of the subclavian are the thyroid axis, with branches to the neck and shoulders; the internal mammary, with branches to the chest walls, mediastinum, and diaphragm, such as the musculo-phrenic and superior epigastric; and the superior intercostal. At the lower border of the first rib, over which it passes, the name axillary is substituted for subclavian, while at the lower border of the axilla, where it starts down the arm, it is called the brachial artery. At the elbow the brachial divides into the radial and ulnar arteries. [Pg 109] The axillary artery sends branches to the chest and shoulder and is more frequently injured than any other artery except the popliteal. Aneurism may occur in it and is very likely to occur in the thoracic aorta.

The subclavian artery supplies the upper limb, but its vertebral branch goes to the brain, where it joins its counterpart to form the basilar artery. The branches of this artery, along with those from the internal carotid artery, create the circle of Willis at the base of the brain. Other branches of the subclavian include the thyroid axis, which supplies the neck and shoulders; the internal mammary, which feeds the chest walls, mediastinum, and diaphragm, including the musculo-phrenic and superior epigastric branches; and the superior intercostal. As it crosses the lower edge of the first rib, it's called the axillary artery. When it reaches the lower edge of the axilla and starts moving down the arm, it becomes the brachial artery. At the elbow, the brachial artery splits into the radial and ulnar arteries. [Pg 109] The axillary artery branches out to the chest and shoulder and is more prone to injury than any other artery except the popliteal artery. Aneurysms can develop here and are particularly likely to occur in the thoracic aorta.

From the thoracic aorta branches go to various of the chest contents, while the abdominal aorta supplies the abdominal viscera. Among the branches of the abdominal aorta are: the celiac axis, which has a gastric, an hepatic, and a splenic branch; the superior and inferior mesenteric to the intestines; the renal; the suprarenal; the spermatic or ovarian; the inferior phrenic; and the lumbar.

From the thoracic aorta, branches go to various parts of the chest, while the abdominal aorta supplies the abdominal organs. Among the branches of the abdominal aorta are: the celiac axis, which includes a gastric, a hepatic, and a splenic branch; the superior and inferior mesenteric arteries to the intestines; the renal; the suprarenal; the spermatic or ovarian; the inferior phrenic; and the lumbar.

The common iliacs divide at the upper edge of the sacrum into the external and internal iliacs, of which the latter with its branches supplies the walls and viscera of the pelvis and the inner part of the thigh. The external iliac and its branches go to the thigh, leg, and foot.

The common iliacs split at the top edge of the sacrum into the external and internal iliacs. The internal iliac and its branches supply the walls and organs of the pelvis and the inner part of the thigh. The external iliac and its branches extend to the thigh, leg, and foot.

Veins.—Of the veins few need be mentioned by name. The deep veins have the same names as the arteries they accompany, though there are two innominate veins where there is only one innominate artery, the subclavian and internal jugular veins on either side joining to form an innominate vein and the two innominates in turn forming the superior vena cava. Of the superficial veins the external and internal jugular correspond to the common carotid arteries and return the blood from the head and face. The external jugular vein is important because it is the largest superficial vein in the neck and is often cut in suicide. The median vein is found at the bend of the elbow and is used in letting blood and in giving salt solution, while the basilic is on the inner side and the median cephalic on the outer side of the upper arm. Varicosity often occurs in the internal or long saphenous and the external or short saphenous in the leg. The inferior vena cava is formed by the juncture of the two common iliac veins.

Veins.—Of the veins, few need to be named specifically. The deep veins share the same names as the arteries they accompany, although there are two innominate veins where there is only one innominate artery. The subclavian and internal jugular veins on each side come together to form an innominate vein, and the two innominates then merge to create the superior vena cava. Among the superficial veins, the external and internal jugular correspond to the common carotid arteries and carry blood back from the head and face. The external jugular vein is significant because it is the largest superficial vein in the neck and is often cut in cases of suicide. The median vein is located at the bend of the elbow and is used for bloodletting and administering saline solution, while the basilic vein is on the inner side and the median cephalic vein is on the outer side of the upper arm. Varicosity often occurs in the internal or long saphenous and the external or short saphenous veins in the leg. The inferior vena cava is formed by the junction of the two common iliac veins.

Portal Circulation.—The portal system of veins includes four [Pg 110] large trunks which collect the blood from the viscera of digestion, the superior and inferior mesenteric veins from the intestines, the splenic vein from the spleen, and the gastric from the stomach. These join together to form the portal vein, the only vein that breaks up into capillaries. This divides and ramifies through the liver, whence it emerges as the hepatic veins. The whole is known as the portal circulation.

Portal Circulation.—The portal system of veins consists of four [Pg 110] large trunks that gather blood from the digestive organs: the superior and inferior mesenteric veins from the intestines, the splenic vein from the spleen, and the gastric vein from the stomach. These veins come together to form the portal vein, which is the only vein that breaks into capillaries. This then branches throughout the liver, from which it leaves as the hepatic veins. This entire system is known as the portal circulation.

Pulmonary Circulation.—Of the pulmonary circulation and its vessels a few words might also be said. The pulmonary artery, which carries the blood from the right ventricle to the lungs, is only about two inches long and divides into a right and a left pulmonary artery, which pierce the pericardium and go to their respective lungs. The right one is the larger and longer, for it has farther to go and gives off a branch to supply the third lobe of the right lung. The vessels finally divide and subdivide, terminating in the pulmonary capillaries. The venous capillaries then gather together to form a main vein in each lobule, these veins uniting into two trunks for each lung, the pulmonary veins, which empty into the left auricle.

Pulmonary Circulation.—A few words can also be said about the pulmonary circulation and its vessels. The pulmonary artery, which carries blood from the right ventricle to the lungs, is only about two inches long and splits into a right and a left pulmonary artery, which pass through the pericardium and go to their respective lungs. The right one is larger and longer because it has a longer distance to cover and gives off a branch to supply the third lobe of the right lung. The vessels eventually branch out and split, ending in the pulmonary capillaries. The venous capillaries then come together to form a main vein in each lobule, with these veins joining into two trunks for each lung, the pulmonary veins, which empty into the left atrium.

Nerves of Heart.—The muscular fibers of the heart have the power of rhythmical contraction. Independent nerve centers or ganglia are also found in the muscular walls and influence the mechanism of the heart, especially the acceleratory mechanism. Thus, in some of the lower animals the heart can be removed from the body, and if placed in normal salt solution will go on beating for some time. The heart is controlled, however, by two nerves, the vagus or pneumogastric and the sympathetic. Of these the vagus is the inhibitory mechanism. It acts as a check and makes the heart’s action regular and rhythmic. If it is cut, the action of the heart becomes very rapid and irregular. The sympathetic is the acceleratory mechanism. When the vagus alone is stimulated, it first slows, then stops the heart, for it weakens the systole and prolongs diastole. Acceleration follows stimulation of the [Pg 111] sympathetic, both the rapidity and the force of the beat being increased. When a person faints from a blow in the abdomen, it is because the pneumogastric is affected and inhibits the action of the heart. The work of the heart is very dependent upon its nervous condition and functional diseases of the heart are practically wholly due to nervous derangement.

Nerves of the Heart.—The heart's muscle fibers can contract rhythmically. There are independent nerve centers or ganglia in the heart's muscular walls that influence its mechanisms, especially the speed of the heartbeat. In some lower animals, the heart can be taken out of the body and, if placed in a normal salt solution, will continue beating for a while. However, two nerves control the heart: the vagus (or pneumogastric) and the sympathetic. The vagus serves as the inhibitory mechanism, regulating the heart's action to keep it steady and rhythmic. If it's severed, the heart beats very quickly and erratically. The sympathetic nerve acts as the acceleratory mechanism. Stimulating the vagus nerve initially slows the heart and may stop it entirely, as it weakens the contraction and prolongs the relaxation phase. Acceleration occurs when the sympathetic nerve is stimulated, increasing both the speed and strength of the heartbeat. When someone faints from a blow to the abdomen, it’s because the pneumogastric nerve is affected, inhibiting the heart's action. The heart's function is highly influenced by its nerve condition, and functional heart diseases are almost entirely caused by nervous issues.

Heart Sounds.—Through the stethoscope two heart sounds may be heard. They are known as the first and second sounds. The first is a soft, rushing sound, stronger and louder than the other, and is caused in part by the contraction of the muscle itself when the blood is forced out and in part by the closure of the auriculo-ventricular valves. The second sound is shorter and sharper, a snap, and is caused by the closure of the semilunar valves when the contraction of the ventricles ceases and they begin to refill. In certain diseased conditions, where the edges of the valves are roughened, they do not snap properly and the sound varies from the normal.

Heart Sounds.—When using a stethoscope, two heart sounds can be heard. They are called the first and second sounds. The first sound is a soft, rushing noise, stronger and louder than the second, and it’s partly caused by the contraction of the heart muscle when blood is pumped out, as well as the closure of the atrioventricular valves. The second sound is shorter and sharper, like a snap, and it occurs when the semilunar valves close as the ventricles stop contracting and start to refill. In certain medical conditions, where the edges of the valves are rough, they may not snap correctly, and the sound differs from the normal.

The Heart Beat.—The rate of the heart beat is proportionate to the size of the person and increases in rapidity as the size diminishes. If the ear is placed over the abdomen of a pregnant woman, the heart of the fetus can be heard beating very rapidly. In prolonged labor it may become more rapid or very faint and warn the doctor that something should be done. The usual rate of the pulse in the fetus is 140 to 150 times a minute, though it varies with size and sex. At birth it drops to 140 to 130; for the first year it is 130 to 115; for the second year 115 to 105; for the third year 105 to 95; from the seventh to the fourteenth years 80 to 90; from the fourteenth to the twenty-first years 75 to 80; from twenty-one to sixty 60 to 75. In old age it rises a little and is 75 to 80. The rate is higher in the average woman than in the average man and increases with exercise, with increase of temperature, and in high altitudes, where the atmospheric pressure is less.

The Heart Beat.—The heart rate is related to a person's size and gets faster as the size gets smaller. If you listen closely to the abdomen of a pregnant woman, you can hear the fetus's heart beating very quickly. During prolonged labor, the heartbeat may speed up or become very faint, signaling to the doctor that action may be needed. The typical fetal heart rate is 140 to 150 beats per minute, although it varies with size and sex. At birth, it drops to 140 to 130; throughout the first year, it is 130 to 115; for the second year, it is 115 to 105; for the third year, 105 to 95; from ages seven to fourteen, it ranges from 80 to 90; from fourteen to twenty-one, it is 75 to 80; and from twenty-one to sixty, it is 60 to 75. In old age, it increases slightly to 75 to 80. The average woman's heart rate is higher than the average man's and it rises with exercise, increased temperature, and at high altitudes, where the air pressure is lower.

At each beat of the heart from four to six ounces of blood are expelled [Pg 112] into the pulmonary artery and the aorta, and in 22 or 23 beats all the blood in the body passes through the heart. The power exerted by the heart every minute in thus driving the blood upon its course has been estimated as sufficient to raise its own weight, three-quarters of a pound, the height of the Washington monument or 150 meters; for the ventricles have to force the blood into vessels already full.

At each heartbeat, between four and six ounces of blood are pushed out [Pg 112] into the pulmonary artery and the aorta, and in 22 or 23 beats, all the blood in the body passes through the heart. The strength the heart uses every minute to pump the blood along its path is estimated to be enough to lift its own weight, three-quarters of a pound, to the height of the Washington Monument or 150 meters; this is because the ventricles have to push the blood into vessels that are already full.

Factors Affecting Circulation.—There are three main factors in the circulation: 1. the systole, which gives the blood its first impulse; 2. the peripheral resistance in the capillaries, which serves to hold it in check, slowing the circulation and doing away with its rhythmic character, and 3. the elasticity of the walls of the arteries.

Factors Affecting Circulation.—There are three main factors in circulation: 1. the systole, which provides the initial push for the blood; 2. the peripheral resistance in the capillaries, which helps to slow it down, affecting the circulation rhythm; and 3. the elasticity of the artery walls.

If a ligature is tied about an artery, there is a swelling on the side toward the heart, while in the case of a vein, the swelling is on the side away from the heart, that is, the swelling is in either case on the side from which the blood comes. When an artery is cut, however, the blood comes out rhythmically in spurts, though from a cut vein it oozes slowly and regularly. For the blood is pumped out by the heart rhythmically and its rhythmic beating against the walls of the artery is felt in the pulse, which follows slightly after the beat of the heart itself. The pulse is due to the fact that the vessels into which the blood is forced are already full. This causes a local dilation at the beginning of the artery which passes with diminishing force along its entire length, the distention being due to the fact that more force is needed to drive the blood through the small arteries and capillaries than to stretch the elastic walls of the aorta and the large arteries. It is this elastic character of the arteries that makes the blood flow constant, for otherwise the blood would come intermittently in jets, as it is pumped from the heart. The elastic walls of the vessels, however, offer a certain resistance to the pumping of the fluid through them and at the same time, by relaxing between whiles, allow a certain amount of fluid to be retained in them, so that they continue full and the flow [Pg 113] is more or less constant. The insufficient outlet also helps to make the flow constant.

If a tie is placed around an artery, there’s a bulge on the side facing the heart, while with a vein, the bulge appears on the side away from the heart, meaning the swelling is on the side where the blood is coming from. However, when an artery is cut, blood spurts out rhythmically, while from a cut vein, it oozes slowly and steadily. This is because blood is pumped rhythmically by the heart, and this rhythmic pulse can be felt in the pulse, which comes slightly after the heartbeat. The pulse happens because the vessels receiving the blood are already full. This creates a local expansion at the start of the artery that diminishes in force along its length, as it requires more effort to push blood through the smaller arteries and capillaries than to stretch the elastic walls of the aorta and larger arteries. It’s this elastic quality of the arteries that keeps the blood flow steady; otherwise, blood would flow in bursts as it’s pumped from the heart. The elastic vessel walls provide some resistance to the fluid being pumped through them, while also allowing some fluid to be held in them by relaxing periodically, keeping them full and the flow [Pg 113] steady. The limited outlet also contributes to maintaining a consistent flow.

By the time the blood reaches the veins its rhythmic character has been done away with, but though there are no elastic walls in the veins, it still has force enough after the slowing in the capillaries to return to the heart. In this it is aided to a certain extent by the valves and by the action of the skeletal muscles as they contract and expand, especially in the arms and legs, where the blood runs perpendicularly and there is a high column to be supported. There are also more veins than arteries, each large artery having two large veins, the venæ comites, to help get the blood back to the heart, and the veins anastomose freely. Thus, if the blood cannot get back by one channel it does by another. In parts like the brain, where it is very important that there should be no compression, since any disturbance of circulation would lead to serious results, the vessels are enclosed in thick walls, and in the liver, through which all the blood passes and where compression is sure to cause trouble, the veins are simply caverns carved out in the organ and have no walls. They lie open when the organ is opened. Varicose veins are the result of valves giving way through inherited weakness or disease so that others have an unduly large weight to support.

By the time blood reaches the veins, its rhythmic quality is gone, but even without elastic walls, it still has enough force after slowing down in the capillaries to return to the heart. The valves and the action of skeletal muscles contracting and relaxing help with this, especially in the arms and legs, where blood flows upward against gravity and has to be supported. There are also more veins than arteries; each large artery has two large veins, called venæ comites, to help return blood to the heart, and the veins connect freely. So, if blood can't get back through one pathway, it can find another. In areas like the brain, where it’s crucial to avoid compression (since any disruption in circulation could have serious consequences), the vessels are surrounded by thick walls. In the liver, which processes all the blood and is prone to complications from compression, the veins are simply cavities carved in the organ and have no walls. They remain open when the organ is accessed. Varicose veins occur when valves fail due to inherited weakness or disease, causing others to carry an excessive load.

The Pulse.—The pulse wave is characterized by a quick rise and a slow fall, though this cannot ordinarily be distinguished by the finger. In some slow fevers, however, the fall is very long and distinct ripples can be felt. This is known as the dicrotic pulse. With age the arterial walls grow stiffer and more rigid and less adapted to their work. In certain cases of heart disease the heart does not transmit all the beats to the pulse and to get the true rate the heart must be listened to.

The Pulse.—The pulse wave has a quick rise and a slow fall, but you usually can’t tell this by feeling it. In some slow fevers, though, the fall is very prolonged and you can feel distinct ripples. This is called the dicrotic pulse. As we age, the arterial walls become stiffer and less flexible, which affects their function. In certain heart diseases, the heart doesn’t transmit all the beats to the pulse, so to get the accurate rate, you need to listen to the heart.

The rate at which the pulse wave travels varies with the size of the artery and the force of the heart beat but is about 15 to 20 feet a second. The flow is most rapid in the arteries because they are nearest [Pg 114] the heart, where the pressure is greatest, and slowest in the capillaries, where the area is greatest, the sectional area of the capillaries, known as the peripheral area because it is farthest from the heart, being larger than that of the large arteries. Thus rapidity of flow varies with pressure and with area.

The speed of the pulse wave depends on the size of the artery and the strength of the heartbeat, averaging around 15 to 20 feet per second. The flow is fastest in the arteries because they are closest to the heart, where the pressure is highest, and slowest in the capillaries, where the area is largest. The sectional area of the capillaries, referred to as the peripheral area since it is farthest from the heart, is larger than that of the large arteries. Therefore, the speed of flow changes with pressure and area.

Blood Pressure.—Liquids, moreover, are incompressible and exert pressure on the walls of the tubes through which they pass. The amount of pressure depends upon the inflow and outflow, increasing directly with the inflow and inversely with the outflow, that is, the smaller the outlet the greater the pressure, and vice versa. The pressure is also greatest nearest to the inflow and gradually decreases with distance until at the point of outflow there is practically no pressure. So, in the arteries the blood pressure is greatest in the large vessels nearer the heart and gradually decreases as they branch into smaller and smaller vessels. In passing through the capillaries, owing to their small size and resultant increased friction, the blood meets with more resistance, the peripheral resistance, and this resistance usually regulates the pressure in the arteries. The greater the peripheral resistance, as a rule, the greater the arterial pressure. The pressure in the capillaries is very slight and in the veins there is practically no pressure. In fact, in the large veins near the heart the pressure is negative and the blood is almost sucked into the heart.

Blood Pressure.—Liquids are incompressible and exert pressure on the walls of the tubes they flow through. The level of pressure depends on how much liquid is coming in and going out, increasing directly with the inflow and decreasing with the outflow; in other words, the smaller the outlet, the greater the pressure, and vice versa. The pressure is highest closest to the inflow and gradually drops as you move further away, until at the point of outflow, there's almost no pressure. So, in the arteries, blood pressure is highest in the large vessels near the heart and gradually lowers as they split into smaller vessels. As blood moves through the capillaries, their small size and increased friction create more resistance, known as peripheral resistance, which usually controls the pressure in the arteries. Generally, the greater the peripheral resistance, the higher the arterial pressure. The pressure in the capillaries is very low, and in the veins, there's practically no pressure. In fact, in the large veins close to the heart, the pressure is negative, and blood is almost pulled into the heart.

Pressure, then, is greatest in the arteries and least in the veins, while the rate of flow is fastest in the arteries—300 to 500 millimeters a second—and slowest in the capillaries—75 millimeters a second—being a little faster again in the veins—200 millimeters a second.

Pressure is highest in the arteries and lowest in the veins, while the flow rate is fastest in the arteries—300 to 500 millimeters per second—and slowest in the capillaries—75 millimeters per second—being slightly faster again in the veins—200 millimeters per second.

Blood pressure is gauged by opening a vessel and inserting a manometer, the pressure being determined by the height to which the mercury is raised. In man the pressure in the arteries is 120 to 160 [Pg 115] millimeters. It is considerably heightened during inspiration by the increased pressure of the lungs on the heart and great vessels. In pericarditis the opposite is true.

Blood pressure is measured by opening a blood vessel and inserting a manometer, with the pressure indicated by how high the mercury rises. In humans, the pressure in the arteries is between 120 to 160 [Pg 115] millimeters. It significantly increases during inhalation due to the added pressure from the lungs on the heart and major blood vessels. However, in cases of pericarditis, the opposite occurs.

When the blood pressure is high, the pulse is small and travels fast, because the wall of the artery is already highly stretched. Such a pulse is hard and incompressible. A large pulse occurs where the heart is strong and the pressure is low, owing to peripheral dilatation. A low-pressure pulse is soft and compressible if the heart beat is weak. A slow pulse is generally stronger than a rapid one.

When blood pressure is high, the pulse is small and moves quickly because the artery wall is already stretched a lot. This type of pulse feels hard and can’t be compressed. A large pulse happens when the heart is strong and the pressure is low due to wider blood vessels. A low-pressure pulse feels soft and can be compressed if the heartbeat is weak. Generally, a slow pulse is stronger than a fast one.

The nerve supply of the blood-vessels comes from the spinal cord through the vasomotor nerves, which are connected with the sympathetic system and are distributed to the smooth muscle fibers of the vessels. They are of two classes, the vasoconstrictors, which diminish the lumen of the vessels, and the vasodilators, which increase the size of the vessels. By these nerves the general tone of the arteries is kept up. They are distributed chiefly to vessels in the skin and in the abdominal organs and the constrictors are probably the more important. When the constrictors are stimulated, three phenomena occur: 1. diminished flow through the vessel, due to its diminished size; 2. increased general arterial pressure, and 3. increased flow through the other arteries. When the dilators are stimulated the opposite effect is produced: 1. the flow through the vessel is increased; 2. there is decreased arterial pressure, and 3. there is decreased flow through the other arteries. The palor of fright is due to the action of the vasoconstrictor nerves of the face and blushing to the action of the vasodilators. Heat stimulates the vasodilators so that more blood goes to the skin, perspiration begins, and the body is cooled by evaporation. Cold stimulates the vasoconstrictors and the blood is kept within the body, where it cannot cool. If a part has too much blood, an impulse passes by the vasoconstrictors to lessen the supply, while if [Pg 116] more blood is needed a message goes to the central nervous system and an impulse passes by the vasodilators to flush the organ. The more active a part is in functioning the greater the number of capillaries, except in the brain, which has only large vessels. The vessels of the intestines contain much blood and are capable of containing all the blood in the body.

The nerve supply of the blood vessels originates from the spinal cord via the vasomotor nerves, which connect to the sympathetic system and are distributed to the smooth muscle fibers of the vessels. There are two types: vasoconstrictors, which narrow the lumen of the vessels, and vasodilators, which widen the vessels. These nerves help maintain the overall tone of the arteries. They primarily target vessels in the skin and abdominal organs, with constrictors likely being the more significant. When the constrictors are activated, three things happen: 1. reduced flow through the vessel due to its smaller size; 2. increased overall arterial pressure; and 3. increased flow through the other arteries. When the dilators are activated, the opposite occurs: 1. flow through the vessel increases; 2. arterial pressure decreases; and 3. flow through other arteries decreases. The paleness from fear results from the action of the vasoconstrictor nerves in the face, while blushing is due to the vasodilators' action. Heat activates the vasodilators, allowing more blood to flow to the skin, triggering perspiration, and cooling the body through evaporation. Cold activates the vasoconstrictors, reserving blood within the body to prevent cooling. If a part has excess blood, a signal travels through the vasoconstrictors to reduce the supply, whereas if more blood is needed, a message is sent to the central nervous system, and an impulse travels through the vasodilators to increase blood flow to that area. The more active a region is, the higher the number of capillaries, except in the brain, which has only larger vessels. The vessels in the intestines hold a significant amount of blood and can contain all the blood in the body.

The Blood.—The blood itself, which thus circulates through the body, carrying nutrition to the tissues and removing waste, is a complex fluid of a bright red color. Its amount has been calculated to be about one-thirteenth of the body weight. One-fourth of it is generally in the heart, lungs, and large arteries and veins, one-fourth in the liver, one-fourth in the skeletal muscles, and one-fourth variously distributed through the other organs. If there is too little blood, the vital processes cannot go on as they should, while too great a supply causes weakness rather than strength. So the tendency is to keep the amount constant and any blood added is disposed of and any blood lost is replaced. In starvation it is the last tissue to be used up, for on it the life of the other tissues depends.

The Blood.—The blood that circulates throughout the body delivers nutrients to the tissues and removes waste. It's a complex fluid with a bright red color. It's estimated to make up about one-thirteenth of a person's body weight. Typically, one-fourth of blood is found in the heart, lungs, and large arteries and veins, one-fourth in the liver, one-fourth in the skeletal muscles, and one-fourth distributed among other organs. If there isn't enough blood, vital processes can't function properly, while too much blood can lead to weakness instead of strength. The body tends to maintain a constant blood supply, getting rid of any excess and replacing blood that is lost. During starvation, blood is the last resource to be depleted, as the survival of other tissues depends on it.

Composition.—In composition the blood is practically the same in all arteries and fundamentally the same everywhere, but in passing through certain organs certain substances are added to or taken from it, so that its character changes more or less. Thus it varies somewhat in composition in different parts of the body, as in the liver and kidneys. It has five main functions: 1. the conveying of fuel from the digestive tract to the tissues, or force production; 2. the carrying of oxygen to the tissues; 3. the carrying of tissue-building materials, or tissue building; 4. the distribution of heat; and 5. the removal of waste products.

Composition.—In terms of composition, the blood is pretty much the same in all arteries and essentially the same everywhere, but as it passes through certain organs, some substances are added to or removed from it, causing its character to change to some extent. So, its composition varies a bit in different parts of the body, like in the liver and kidneys. It has five main functions: 1. delivering fuel from the digestive system to the tissues, or generating energy; 2. transporting oxygen to the tissues; 3. providing materials for building tissues, or growing tissue; 4. distributing heat; and 5. eliminating waste products.

The blood is slightly alkaline in reaction, of a saltish taste, and has a specific gravity of 1055. Its temperature is about 100° Fahrenheit or 37.8° Centigrade. It is made up of two parts, the plasma or fluid [Pg 117] portion and the corpuscles or solid portion. The plasma, again, which is transparent and almost colorless, consists of two materials, the blood serum and fibrin. Fibrin does not exist as such in the body nor in freshly shed blood, but there is a substance named fibrinogen which is worked on by another substance, the fibrin ferment, to form fibrin. Both fibrin ferment and fibrinogen can be isolated from the blood.

The blood is slightly alkaline, has a salty taste, and has a specific gravity of 1.055. Its temperature is around 100° Fahrenheit or 37.8° Celsius. It consists of two parts: the plasma or liquid part and the corpuscles or solid part. The plasma, which is clear and nearly colorless, is made up of two components, blood serum and fibrin. Fibrin doesn't exist in the body or in freshly drawn blood, but there is a substance called fibrinogen that is acted upon by another substance, fibrin ferment, to create fibrin. Both fibrin ferment and fibrinogen can be extracted from the blood.

Coagulability.—In the body the blood is perfectly fluid and under normal conditions does not coagulate. But, though fluid when first shed, upon standing it gradually becomes viscid, that is, in two or three minutes, then jelly-like, in five to ten minutes, and grows firmer and firmer until there finally appears around this jelly-like mass or clot a yellowish fluid, the serum. The clot is made up of the corpuscles and fibrin. If some blood is drawn and set on ice until the corpuscles settle, the plasma can then be drawn off, and after it has stood a while in a warm place coagulation will take place, a mass of fibrin forming in the middle. It takes from one to two hours for clotting to be complete. In very slow clotting at a low temperature the white corpuscles appear in a layer on top of the clot, the buffy coat.

Coagulability.—In the body, blood is completely fluid and doesn’t coagulate under normal conditions. However, after it’s shed, it’s fluid at first, but after a few minutes, it starts to thicken, becoming gooey in two to three minutes, then jelly-like in five to ten minutes, and it continues to thicken until a yellowish fluid, called serum, appears around the jelly-like mass or clot. The clot consists of corpuscles and fibrin. If some blood is taken and kept on ice until the corpuscles settle, the plasma can then be removed, and after it sits in a warm place for a while, coagulation occurs, with a mass of fibrin forming in the center. Clotting usually takes about one to two hours to complete. In cases of very slow clotting at low temperatures, a layer of white corpuscles appears on top of the clot, known as the buffy coat.

Of fibrin little is known, but its formation is the most important step in clotting, as its presence is absolutely essential. If it is removed by whipping, the blood will not clot. It is a delicate, stringy material, elastic and contractile, and contains certain salts of lime and magnesium, upon whose presence its power of coagulation depends. The coagulability of blood differs in different people and is occasionally so little as to make operation dangerous.

Of fibrin, not much is known, but its formation is the most crucial step in clotting since it's absolutely essential. If it's removed by whipping, the blood won't clot. It's a delicate, stringy substance that's elastic and can contract, containing specific salts of lime and magnesium, which are necessary for its coagulation ability. The ability of blood to clot varies among individuals and can sometimes be so minimal that it makes surgery risky.

The most favorable temperature for clotting is that of the body, extreme heat preventing it and cold delaying it. That the blood does not clot in the body must be due to some relation between the blood and the walls of the arteries and veins that prevents it, just as the walls of the stomach are not digested by the juices secreted. Though [Pg 118] coagulation does not normally take place in the body, it does take place when a blood-vessel is injured or when the blood comes in contact with the air, a wise provision of nature, as otherwise the tendency would be for bleeding to go on indefinitely after injury. The greater the surface with which the blood comes in contact the more quickly it clots. Injury to the vessel wall itself is necessary; the endothelium must be cracked. Under extreme injury the muscular coat of the vessel undergoes spasmodic contraction and partially closes it. Hence a wound caused by tearing is less likely to bleed than one due to cutting.

The best temperature for blood clotting is that of the body; extreme heat stops it, and cold slows it down. The fact that blood doesn’t clot inside the body must be due to some relationship between the blood and the walls of the arteries and veins that prevents it, similar to how the stomach walls aren’t digested by the secreted juices. Although [Pg 118] coagulation normally doesn’t occur in the body, it does happen when a blood vessel is injured or when blood contacts the air, which is a smart design of nature, as otherwise bleeding could continue indefinitely after an injury. The larger the surface area that blood comes into contact with, the quicker it clots. Damage to the vessel wall itself is necessary; the endothelium needs to be damaged. Under severe injury, the muscle layer of the vessel tightens up, partially closing it. Therefore, a tear is less likely to bleed than a clean cut.

The valves of the heart, which are covered with endothelium, are frequently the seat of fibrin coagulation, bits of the fibrin thus formed giving rise to conditions in various kinds of heart trouble. Or the bits of fibrin float in the blood and perhaps lodge in the small vessels of the brain and cause apoplexy. Pus in various parts of the body will set up coagulation in nearby arteries. In fact, the presence of any foreign substance in the blood causes clotting.

The heart valves, lined with a layer of endothelial cells, often experience fibrin coagulation, and the resulting fibrin fragments can lead to different types of heart issues. These fibrin pieces can also circulate in the blood and may get stuck in the small vessels of the brain, potentially causing a stroke. Pus in different areas of the body can trigger coagulation in nearby arteries. In general, the presence of any foreign substance in the blood leads to clotting.

Fig. 45.—Cells of blood: a, Colored blood-corpuscles seen on the flat; b, on edge; c, in rouleau; d, blood platelets. (Leroy.)

Fig. 45.—Blood cells: a, colored blood cells viewed flat; b, viewed on edge; c, in rouleaux; d, blood platelets. (Leroy.)

Blood-corpuscles.—The solid parts of the blood are the red corpuscles, the white corpuscles, and the blood plaques or plates. It is to the red corpuscles, or erythrocytes which number about 5,000,000 to the cubic millimeter of blood, that the color of the blood is due. Under the microscope they appear as small, spherical, biconcave [Pg 119] discs with a slightly greenish-yellow color, which have a tendency to form in rouleaux. They are homogeneous, with no limiting membrane, and are made up of a fine network of tissue, the stroma, in which is embedded the hemoglobin or coloring matter. This hemoglobin is a crystalline body and the most complex substance known to chemists. The corpuscles are very flexible and can squeeze through small apertures, as in the tiny capillaries, and regain their shape. They are probably formed chiefly in the red bone marrow at the ends of the bones, which under the microscope shows red corpuscles in various stages of growth, and also in the spleen, for which no other use is known. Their function is to carry oxygen, which forms a chemical combination, though an extremely loose one, with the hemoglobin. As the tissues are more greedy of oxygen than is the hemoglobin, they rob the corpuscles of it.

Blood Cells.—The solid components of blood include red blood cells, white blood cells, and blood platelets. The red blood cells, or erythrocytes, which number about 5,000,000 per cubic millimeter of blood, give blood its color. Under a microscope, they look like small, round, biconcave discs with a slightly greenish-yellow hue, often forming stacks called rouleaux. They are uniform, without a limiting membrane, and consist of a delicate network of tissue, the stroma, which contains hemoglobin, the pigment responsible for color. Hemoglobin is a crystalline substance and is the most complex material known to chemists. The cells are very flexible, allowing them to squeeze through tiny openings, like those in capillaries, and return to their original shape. They are primarily produced in the red bone marrow at the ends of bones, where you can see red blood cells at various stages of development under a microscope, and also in the spleen, which seems to have no other known function. Their main role is to transport oxygen, which forms a very loose chemical bond with hemoglobin. Since tissues require more oxygen than hemoglobin holds, they take it from the red blood cells.

Fig. 46.—Various forms of leucocytes: a, Small lymphocyte; b, large lymphocyte; c, polymorphonuclear neutrophile; d, eosinophile. (Leroy.)

Fig. 46.—Different types of white blood cells: a, small lymphocyte; b, large lymphocyte; c, polymorphonuclear neutrophil; d, eosinophil. (Leroy.)

The white corpuscles or leucocytes are much fewer in number, about one to from 300 to 700 of the red, the average number being 5,000 to 10,000 to the cubic millimeter. They are larger than the red corpuscles, colorless, and spherical when at rest. Their structure is more definite, there being a definite cell substance or protoplasm and one or more nuclei, which vary more or less in shape and size. The corpuscles are classed in accordance with these variations in the nuclei. They are most numerous during digestion and are probably formed in the lymphatic system, constantly passing from the lymphatics to the [Pg 120] arteries and veins. For they have the function of amœboid movement by which they not only wander from place to place in the blood, keeping close to the sides of the vessels, but pass through the walls of the capillaries, probably between the cells which form their lining, into the lymph spaces. This is known as migration of the white corpuscles. In inflammation they collect in the inflamed area to assist in allaying the inflammation by absorbing and carrying off its products. For they carry waste products and destroy poisons, acting as scavengers and protectors of the body. When they are unsuccessful and the inflammation gets the better of them, they become pus corpuscles.

The white blood cells or leucocytes are much less numerous, about one for every 300 to 700 red blood cells, with an average count of 5,000 to 10,000 per cubic millimeter. They are larger than red blood cells, colorless, and spherical when at rest. Their structure is more defined, consisting of a clear cell substance or protoplasm and one or more nuclei, which can vary in shape and size. The cells are categorized based on these variations in the nuclei. They are most abundant during digestion and are likely produced in the lymphatic system, constantly moving from the lymphatics into the [Pg 120] arteries and veins. Their role involves amœboid movement, allowing them to not only roam through the blood while staying close to the vessel walls but also to pass through the capillary walls, likely between the cells that make up their lining, into the lymph spaces. This process is referred to as migration of the white blood cells. During inflammation, they gather in the affected area to help reduce the inflammation by absorbing and removing its byproducts. They carry away waste products and neutralize toxins, acting as scavengers and protectors of the body. When they fail to manage the situation and inflammation overwhelms them, they become pus cells.

Besides the corpuscles there are seen floating in the blood small disk-like substances with no special characteristics, the blood plaques or plates, whose function is unknown.

Besides the corpuscles, there are small disk-like substances floating in the blood with no special characteristics, the blood plates or plates, whose function is unknown.

In anemia the red corpuscles are diminished and the white corpuscles and blood plaques increased in number. After excessive bleeding normal salt solution is injected, subcutaneously or by rectum, as being nearly equivalent to blood serum in composition, and the renewal of the solid elements is left to time. The length of time needed for their restoration is about a week, except in the case of the hemoglobin, which takes longer.

In anemia, the number of red blood cells is decreased while the white blood cells and platelets are increased. After severe bleeding, a normal saline solution is injected either under the skin or rectally since it closely resembles blood serum in its makeup. The restoration of the solid components is a process that takes time. It generally takes about a week for them to recover, except for hemoglobin, which takes longer.


CHAPTER IX.
THE LUNGS AND BREATHING.

Besides the heart and the great vessels the chest contains the lungs, the chief organ of respiration, which, with the rest of the respiratory system, will now be treated. The nose and mouth, through which the air first enters the body, have already been spoken of. From them the air passes through the larynx to the trachea, thence to the bronchi, and so to the lungs, where the supply of oxygen for the tissues is taken from the air by the hemoglobin of the blood.

Besides the heart and major blood vessels, the chest holds the lungs, the main organ for breathing, which, along with the rest of the respiratory system, will now be discussed. The nose and mouth, where air first enters the body, have already been mentioned. From there, air moves through the larynx to the trachea, then to the bronchi, and finally to the lungs, where the hemoglobin in the blood absorbs oxygen from the air for the tissues.

The Larynx.The larynx lies in front of the pharynx at the upper and fore part of the neck, where it causes a considerable projection, known as Adam’s apple. It is a triangular box, base up, flattened at the back, in front, and at the sides, but becoming cylindrical below. Above it opens into the bottom of the pharynx and below into the trachea. It is lined with mucous membrane. Its opening at the base of the tongue is closed during swallowing by a little door-like valve of fibro-cartilage, the epiglottis, to prevent the entrance of food.

The Larynx.The larynx is located in front of the pharynx at the upper and front part of the neck, creating a noticeable projection known as the Adam’s apple. It has a triangular shape with the base facing up, flattened at the back, front, and sides, but rounding out below. At the top, it connects to the bottom of the pharynx and below it connects to the trachea. It's lined with mucous membrane. The opening at the base of the tongue is covered during swallowing by a small door-like valve made of fibro-cartilage called the epiglottis, which prevents food from entering.

Nine cartilages go to make up the larynx, of which the most important are the thyroid and cricoid cartilages and the epiglottis already mentioned. The thyroid is the largest and is open behind, its two alæ or wings meeting in an acute angle in front and forming the Adam’s apple, always more prominent in the male than in the female. It is attached above to the hyoid bone and has cornua or horns on either side, top and bottom. The cricoid or ring-like cartilage resembles a seal ring with the stone placed posteriorly. It is stronger than the [Pg 122] thyroid and forms the lower part of the cavity of the larynx. Inside and resting on the upper border of the cricoid are the two smaller arytenoid or pitcher-like cartilages, pyramidal in shape, and surmounting these again the two cornicula laryngis. The two cuneiform cartilages are in the free borders of the folds of mucous membrane which extend from the apex of the arytenoids to the sides of the epiglottis. Numerous small muscles serve to bind these various cartilages together.

Nine cartilages make up the larynx, with the most important being the thyroid and cricoid cartilages, along with the previously mentioned epiglottis. The thyroid is the largest and is open at the back, with its two wings meeting at an acute angle in front, forming the Adam's apple, which is always more noticeable in males than in females. It's attached above to the hyoid bone and has horns on either side, top, and bottom. The cricoid cartilage, shaped like a ring, resembles a seal's ring with the stone at the back. It's thicker than the thyroid and makes up the lower part of the larynx. Resting on the upper edge of the cricoid are the two smaller arytenoid cartilages, shaped like pyramids, and sitting on top of these are the two cornicula laryngis. The two cuneiform cartilages are located in the free edges of the mucous membrane folds that stretch from the tops of the arytenoids to the sides of the epiglottis. Many small muscles help connect these different cartilages together.

At the angle of the thyroid cartilage in front are attached the epiglottis at the top and just below that the superior or false vocal cords, two folds of mucous membrane enclosing the superior thyro-arytenoid ligaments. Lower still are found the inferior or true vocal cords, which are formed by the inferior thyro-arytenoid ligaments covered with a thin, tightly fitting mucous membrane. Both sets of vocal cords as well as the epiglottis may be seen by means of a head and a throat mirror. Between the true vocal cords is a narrow triangular interval called the glottis. It is by means of the vibrations of these cords that sound is produced. The false vocal cords cannot produce sound, though they can modify it indirectly. Quality of voice, as treble, base, etc., depends upon the size of the larynx and the length and elasticity of the vocal cords. Modulation is produced by changing the form of the cavity of the mouth and nose. In whispering the lips take the place of the vocal cords and produce sound by the vibration of their muscular walls.

At the front angle of the thyroid cartilage, the epiglottis is attached at the top, and just below that are the superior or false vocal cords, which are two folds of mucous membrane that enclose the superior thyro-arytenoid ligaments. Lower down are the inferior or true vocal cords, made up of the inferior thyro-arytenoid ligaments covered by a thin, snug mucous membrane. Both sets of vocal cords and the epiglottis can be seen using a head and throat mirror. Between the true vocal cords is a narrow triangular space called the glottis. Sound is produced through the vibrations of these cords. The false vocal cords cannot create sound, but they can modify it indirectly. The quality of voice, such as treble or bass, depends on the size of the larynx and the length and elasticity of the vocal cords. Modulation happens by changing the shape of the mouth and nasal cavity. When whispering, the lips act like the vocal cords, producing sound through the vibration of their muscular walls.

Instead of tracheotomy laryngotomy is sometimes done in the depression between the thyroid and the cricoid, which may be felt on the living. Foreign bodies sometimes get into the larynx and have to be removed, or the mucous membrane may become inflamed, causing laryngitis. Syphilis attacks the larynx, and tuberculosis and cancer of the larynx occur, these last two being generally fatal. Edema of the glottis may also occur. [Pg 123]

Instead of a tracheotomy, a laryngotomy is sometimes performed in the space between the thyroid and the cricoid, which can be felt on a living person. Foreign objects can sometimes get lodged in the larynx and need to be removed, or the mucous membrane may become inflamed, leading to laryngitis. Syphilis can affect the larynx, and tuberculosis and cancer of the larynx can occur, with the last two generally being fatal. Edema of the glottis can also happen. [Pg 123]

Fig. 47.—The larynx, trachea and bronchi
(After Sobotta.)

Fig. 47.—The larynx, trachea, and bronchi
(After Sobotta.)

The Trachea.The trachea is a membranous tube extending down from the larynx for about four and a half inches to the fourth or fifth dorsal vertebra, where it divides into the right and left bronchi. It is formed of sixteen to twenty imperfect cartilaginous rings, open behind, enclosed in a double elastic fibrous membrane, and is lined with ciliated mucous membrane. The rings are for strength and in the interval at the back where they are wanting there is one layer of longitudinal and another of transverse unstriped muscle fibers. The passage is kept clear by the action of the cilia, which sweep up and out any particles of dust that become entangled in the mucus. Tracheotomy is generally done about one inch below the cricoid, [Pg 124] just above the sternal notch, incision being made through the cartilage.

The Trachea.The trachea is a tube made of membrane that extends down from the larynx for about four and a half inches to the fourth or fifth dorsal vertebra, where it splits into the right and left bronchi. It consists of sixteen to twenty incomplete cartilaginous rings, which are open at the back, surrounded by a double elastic fibrous membrane, and lined with a ciliated mucous membrane. The rings provide strength, and in the gap at the back where they are absent, there is one layer of longitudinal and another of transverse smooth muscle fibers. The passage stays clear thanks to the movement of the cilia, which sweep up and out any dust particles that get caught in the mucus. Tracheotomy is typically performed about one inch below the cricoid, [Pg 124] just above the sternal notch, with an incision made through the cartilage.

Fig. 48.—The upper thorax of a child eight years old, showing the thyroid and thymus glands. (Sobotta.)

Fig. 48.—The upper chest of an eight-year-old child, showing the thyroid and thymus glands. (Sobotta.)

Extending up on either side of the upper trachea in the neck are the two lobes of the thyroid gland, the isthmus, which connects the lobes, covering the trachea below anteriorly. The function of the gland is obscure, but it has an internal secretion of great importance in the metabolic processes. Its removal or disease is followed by general disturbances of mind and body. The injection of thyroid extract has proved effective as treatment. In goiter the gland becomes enlarged. The thymus gland lies below the thyroid gland at birth, in front of and at the sides of the trachea, and runs down behind the sternum. It is largest at the end of the second year, after which it atrophies, being almost absent at puberty. It, too, is ductless and its function is not well understood. [Pg 125]

Extending on either side of the upper trachea in the neck are the two lobes of the thyroid gland, along with the isthmus that connects the lobes and covers the trachea underneath in the front. The gland's function is not entirely clear, but it releases an important internal secretion that plays a significant role in metabolic processes. When it's removed or diseased, it leads to general disturbances in both mind and body. Injecting thyroid extract has shown to be an effective treatment. In goiter, the gland becomes enlarged. The thymus gland is located below the thyroid gland at birth, in front of and beside the trachea, and extends down behind the sternum. It is largest at the end of the second year, after which it shrinks and is nearly absent by puberty. Like the thyroid, it is ductless, and its function is also not well understood. [Pg 125]

The Bronchi.The two bronchi, of which the right is the larger and shorter, resemble the trachea in structure. As they enter the root of the lung they divide, the right into three and the left into two branches, one for each lobe, after which they divide and subdivide, the bronchioles becoming smaller and smaller and finally ending in the infundibula, pouch-like places lined with air cells, in which cilia keep the air in motion. As they grow smaller the bronchioles gradually become wholly membranous.

The Bronchi.The two bronchi, with the right one being larger and shorter, are similar in structure to the trachea. When they enter the lung root, they split, with the right side dividing into three branches and the left side into two, one for each lobe. After this, they keep dividing and splitting, with the bronchioles getting smaller and smaller until they end in the infundibula, pouch-like areas lined with air cells, where cilia keep the air moving. As the bronchioles decrease in size, they gradually become entirely membranous.

Fig. 49.—Relation of lungs to other thoracic organs.
(Ingals.)

Fig. 49.—Relation of lungs to other thoracic organs.
(Ingals.)

The Lungs.The lungs themselves, two in number, lie each in a serous sac or pleura, similar in structure to the pericardium and serving a like purpose. The outer layer of the pleura is reflected back over the thoracic wall and diaphragm. There is no pleural cavity in health between the two layers of the pleura, the two surfaces being in close contact, though moistened with lymph to prevent friction during [Pg 126] respiration. In inflammation of the pleuræ or pleurisy, they become thickened and roughened and friction results, as is shown by the sounds heard through the stethoscope. Friction causes effusion and fluid collects. This generally absorbs again, but occasionally the serous fluid becomes pustular and empyema results.

The Lungs.The lungs are two in number, each located in a serous sac or pleura, which is similar in structure to the pericardium and has a similar function. The outer layer of the pleura wraps around the thoracic wall and diaphragm. In a healthy state, there is no pleural cavity between the two layers of the pleura; the surfaces are in close contact, but they are moistened with lymph to prevent friction during [Pg 126] breathing. In cases of pleural inflammation, or pleurisy, the pleura become thickened and rough, leading to friction, which can be detected by sounds through the stethoscope. This friction can cause fluid buildup. Typically, this fluid gets absorbed again; however, sometimes the serous fluid can become infected, resulting in empyema.

In front, between the two pleuræ, which are wholly separate, is the mediastinal space or mediastinum, which extends from the sternum to the spinal column and contains all the thoracic viscera except the lungs and heart, that is, the trachea, esophagus, thoracic duct, and many large vessels and nerves.

In front of the two pleurae, which are completely separate, is the mediastinal space or mediastinum. This space stretches from the sternum to the spinal column and contains all the thoracic organs except for the lungs and heart, including the trachea, esophagus, thoracic duct, along with many large vessels and nerves.

Fig. 50.—Diagrammatic representation of the termination of a bronchial tube in a group of infundibula: B, Bronchial tube; LB, bronchiole; A, atrium; I, infundibulum; C, alveoli. (de Nancrede.)

Fig. 50.—Diagram showing how a bronchial tube ends in a group of infundibula: B, Bronchial tube; LB, bronchiole; A, atrium; I, infundibulum; C, alveoli. (de Nancrede.)

Roughly speaking, the lungs begin at the sterno-clavicular articulation above, the apex coming up above the level of the first rib, and extend downward together to the fourth cartilage, where the lower margins gradually separate, the lowest lung limit being the eleventh rib in the vertebral region. Each lung is conical. The apices extend upward and the bases, which are broad and concave, rest upon the diaphragm. The right lung is divided by a fissure into three lobes, the left into two. The root consists of a bronchus and pulmonary arteries, veins, lymphatics, and nerves. The tissue itself is composed of an aggregation of lobules, each consisting of a terminal bronchiole with its alveoli [Pg 127] or air cells, blood-vessels, and nerves, a lung in miniature. The blind pouches which the air cells surround are called infundibula and are separated by delicate membranous septa in which lie the capillaries of the pulmonary artery, thus exposing the blood to the air on two sides. The lung itself is supplied by the bronchial arteries from the thoracic aorta and by branches of the sympathetic and pneumogastric nerves.

Generally speaking, the lungs start at the sterno-clavicular joint at the top, with the apex extending above the first rib, and go down to the fourth cartilage, where the lower edges gradually separate, with the lowest lung limit reaching the eleventh rib in the vertebral area. Each lung is cone-shaped. The apices point upward, while the bases, which are wide and concave, rest on the diaphragm. The right lung is divided by a fissure into three lobes, and the left lung has two. The root includes a bronchus along with pulmonary arteries, veins, lymphatics, and nerves. The lung tissue itself is made up of clusters of lobules, each containing a terminal bronchiole and its alveoli or air cells, along with blood vessels and nerves, resembling a miniature lung. The blind sacs surrounding the air cells are called infundibula and are separated by thin membranous septa which contain the capillaries of the pulmonary artery, allowing blood to be exposed to air on both sides. The lung receives blood supply from the bronchial arteries that come from the thoracic aorta and from branches of the sympathetic and vagus nerves. [Pg 127]

At birth the lungs are pinkish-white in color but in later life they are marked with slate-colored patches, due to the deposit in the lung tissue of particles of dirt breathed in. They are light, spongy, and highly elastic, and will float in water, crepitating upon pressure owing to the air in the tissue.

At birth, the lungs are pinkish-white, but as we age, they develop slate-colored patches because of dirt particles that get trapped in the lung tissue from breathing. They are light, spongy, and very elastic, making them float in water and crackle when pressed because of the air inside them.

At birth, also, the lungs are solid, so that the first air has to overcome adhesions between the collapsed walls of the bronchioles and air sacs, but after they are thus gradually unfolded, in that they are of extensible material and open to the air above, atmospheric pressure from within keeps them distended to the full extent of the chest, which is air tight. They never collapse afterwards unless puncture of the chest wall, as in stabbing, causes collapse, in which case the lung shrivels into a small ball.

At birth, the lungs are also solid, so the first breath has to break the stickiness between the collapsed walls of the bronchioles and air sacs. However, once they are gradually opened up, since they’re made of flexible material and exposed to air, the pressure from inside keeps them fully expanded in the airtight chest. They won’t collapse again unless the chest wall is punctured, like in a stab wound, in which case the lung shrinks down into a small ball.

Respiration.—That the organic materials used by the body as food may give up their energy they must be broken up, and for this oxygen is needed. The supply of oxygen for the purpose is brought to the tissues by the blood, which acquires it in the lungs, and the waste product of combustion, carbon dioxide, is carried off in the same manner. The lungs are, therefore, adapted to take in large quantities of air and to keep up a rapid exchange of oxygen and carbon dioxide in the blood. This process of supplying oxygen to the tissues and of removing carbon dioxide and other waste is ordinarily an involuntary act, though it can be regulated temporarily, and is known as respiration or breathing.

Respiration.—In order for the organic materials that the body uses as food to release their energy, they need to be broken down, and this requires oxygen. The oxygen needed for this process is delivered to the tissues by the blood, which picks it up in the lungs, and the waste product of this process, carbon dioxide, is expelled in the same way. The lungs are designed to take in large amounts of air and to maintain a quick exchange of oxygen and carbon dioxide in the blood. This process of providing oxygen to the tissues and removing carbon dioxide and other waste is usually an involuntary action, although it can be temporarily controlled, and is called respiration or breathing.

There are two periods to respiration: 1. inspiration or the drawing [Pg 128] in of air, and 2. expiration or the expulsion of air from the lungs, the former process being a little shorter than the latter. A pause follows each expiration before there is another inspiration. At birth the normal rate of respiration is 42, but it grows slower as the child grows older, being 26 at the age of five or six, while in the adult it averages 17 to 20 times a minute. It is slower during sleep and more rapid during physical activity. The average amount of air taken in with every inspiration is 30 cubic inches and the minimum air space per individual should be 3000 cubic feet per hour.

There are two phases of respiration: 1. inspiration, which is the intake of air, and 2. expiration, the release of air from the lungs. The first phase is slightly shorter than the second. There is a brief pause after each expiration before the next inspiration. At birth, the normal respiration rate is 42 breaths per minute, but it decreases as the child grows, reaching about 26 breaths at the age of five or six, while in adults it averages between 17 and 20 breaths per minute. Respiration slows during sleep and speeds up during physical activity. On average, each inspiration takes in about 30 cubic inches of air, and the minimum air space per person should be 3000 cubic feet per hour.

Breathing is of two kinds, diaphragmatic or abdominal and chest or rib breathing, the former usually being more pronounced in men than in women, probably because of centuries of tight dressing on the part of the latter. As a rule, however, both diaphragm and ribs come into play; for in inspiration, which is an active movement, the thorax becomes enlarged from before backward, laterally, and vertically. The ribs are raised by the external intercostals chiefly, though the internal intercostals aid somewhat, and swinging out upon the vertebræ, widen the chest as well as deepen it. The diaphragm, which is dome-like when relaxed, becomes flattened in contraction and so increases the size of the chest from above downward. As the chest enlarges, the lungs expand, the air in them becomes rarefied, and more air rushes in. When the lungs are full they relax and the muscles relax after their contraction, so that expiration is a passive movement, due largely to the elastic relaxation of lungs and muscles, the air being driven out by the lessened capacity of the lungs.

Breathing comes in two types: diaphragmatic or abdominal breathing, and chest or rib breathing. The former is usually more noticeable in men than in women, likely due to centuries of tight clothing worn by women. Generally, both the diaphragm and the ribs are used; during inspiration, which is an active movement, the thorax expands from front to back, side to side, and top to bottom. The external intercostal muscles mainly raise the ribs, while the internal intercostals provide some assistance, and as the ribs pivot on the vertebrae, they widen and deepen the chest. The diaphragm, which is dome-shaped when relaxed, flattens when it contracts, increasing the chest size from top to bottom. As the chest expands, the lungs inflate, the air inside becomes less dense, and more air is drawn in. When the lungs are full, they relax along with the muscles after contraction, making expiration a passive process mainly due to the elastic relaxation of the lungs and muscles, with air being expelled as the lung capacity decreases.

Difficult Breathing.—In heart and lung troubles, where too little oxygen is carried to the tissues, dyspnœa or difficult breathing results and may even advance to asphyxia, a condition in which no air is obtained. In difficult or labored respiration the pectoral muscles are used in inspiration and the scaleni, which pass from the vertebræ [Pg 129] of the neck to the sternum, develop and become powerful. The levatores of the ribs may also assist, and even the muscles of the neck and arms may help out, while in forced expiration the abdominal muscles are called into play. The glottis opens and closes rhythmically as the air enters and leaves the lungs, and the nostrils add their mite in the struggle for oxygen. Finally there may be scarcely a muscle in the body that is not striving to aid the respiration, and general convulsions may result, followed by exhaustion and death.

Difficult Breathing.—In heart and lung issues, where not enough oxygen is delivered to the tissues, dyspnea or difficult breathing occurs and can even progress to asphyxia, a state in which no air can be inhaled. During difficult or labored breathing, the chest muscles are engaged for inhalation, and the scalene muscles, which extend from the vertebrae of the neck to the sternum, become strong and well-developed. The levatores of the ribs may help, and even the muscles in the neck and arms may assist, while the abdominal muscles are utilized during forced exhalation. The glottis opens and closes in a rhythmic pattern as air flows in and out of the lungs, and the nostrils contribute to the effort to get more oxygen. Ultimately, nearly every muscle in the body may be working to support breathing, which can lead to general convulsions, followed by exhaustion and potentially death.

Air.—In ordinary breathing the lungs are not used to their full capacity and the air ordinarily used is known as tidal air. In forced inspiration the lungs are filled to their fullest extent and the air then taken in in excess of the tidal air is known as complemental air. In like manner, the difference between the air ordinarily breathed out and that breathed out in forced expiration is known as supplemental air. The sum of these three is the vital capacity of the lungs, while beyond this there is probably some air that is never expelled, the stationary or residual air.

Air.—When we breathe normally, our lungs aren't used to their full capacity, and the air we typically use is called tidal air. During deep inhalation, the lungs expand completely, and the extra air taken in beyond the tidal air is referred to as complemental air. Similarly, the difference between the air we normally exhale and the air expelled during a forceful exhalation is known as supplemental air. The total of these three types of air is the vital capacity of the lungs, while there is likely some air that we never expel, known as stationary or residual air.

Respiratory Sounds.—The entrance and exit of the air is accompanied by respiratory sounds or murmurs, which vary according to their position in the trachea, the bronchi, or the bronchioles and are modified in diseases of the lungs and bronchi, when they are often called râles.

Respiratory Sounds.—The inhaling and exhaling of air produces respiratory sounds or murmurs, which change based on their location in the trachea, bronchi, or bronchioles, and are altered in lung and bronchial diseases, where they are often referred to as râles.

Changes in Air in Lungs.—In passing through the nose and the rest of the respiratory tract the air is warmed to body temperature and saturated with moisture. After its entrance into the lungs various changes take place in it through the mingling of the tidal with the residual air. Thus, it gives up about 4 or 5 per cent. of its oxygen and acquires some 4 per cent. additional carbon dioxide, while the amount of nitrogen remains about the same. By its giving up more oxygen than it receives carbon dioxide, its volume is slightly diminished. [Pg 130] Exhaled air also contains traces of ammonia and certain organic matters, generally the results of decomposition, which give a bad odor to the breath and are more dangerous in a close room than the mere lack of oxygen or the presence of carbon dioxide. Indeed, the amount of oxygen may be very much diminished, being reduced even to 5 or 6 per cent. instead of the normal 21 per cent., without being noticed or giving rise to any immediate bad results. Yet the importance of ventilation is very evident.

Changes in Air in Lungs.—As air travels through the nose and the respiratory tract, it gets warmed to body temperature and is saturated with moisture. Once it enters the lungs, it undergoes various changes as it mixes with tidal and residual air. It loses about 4 or 5 percent of its oxygen and gains about 4 percent more carbon dioxide, while the nitrogen level stays pretty much the same. Because it gives up more oxygen than it takes in carbon dioxide, its volume decreases slightly. [Pg 130] Exhaled air also contains traces of ammonia and certain organic compounds, usually resulting from decomposition, which can make the breath smell bad and are more hazardous in a confined space than just having low oxygen or high carbon dioxide levels. In fact, the oxygen levels can drop significantly, even down to 5 or 6 percent instead of the normal 21 percent, without anyone noticing or causing immediate harmful effects. Still, the need for ventilation is very clear.

Effect on Blood.—Respiration causes changes also in the blood, the venous blood being purple and the arterial bright red. This difference in color is due to the absence or presence of oxygen, which is not absorbed or dissolved by the blood but forms a rather unstable compound, oxyhemoglobin, with the hemoglobin of the blood. As the oxygen is removed in the passage of the blood through the body, there results in venous blood reduced hemoglobin, which is of a purplish color. Upon exposure to the air, however, it absorbs oxygen once more and resumes its scarlet color. If carbon monoxide gets into the blood, as in cases of gas poisoning, it drives off the oxygen and forms a more stable compound with the hemoglobin, whence the difficulty in restoring a person so poisoned.

Effect on Blood.—Breathing also changes the blood, with venous blood appearing purple and arterial blood looking bright red. This color difference is due to whether oxygen is present or absent. Oxygen doesn’t get absorbed or dissolved by the blood but creates an unstable compound called oxyhemoglobin with the hemoglobin in the blood. As the oxygen is used up while the blood flows through the body, it results in venous blood having reduced hemoglobin, which is purplish in color. However, when exposed to air, it picks up oxygen again and turns back to its bright red color. If carbon monoxide enters the blood, like in cases of gas poisoning, it displaces the oxygen and forms a more stable compound with the hemoglobin, making it difficult to treat someone who has been poisoned.

Nervous Mechanism.—Nervously, respiration is controlled in three ways: 1. by the phrenic nerve to the diaphragm; 2. by some fibers of the vagus or pneumogastric, and 3. by the respiratory center in the bulbous portion of the spinal cord. Injury to the respiratory center means the ceasing of respiration and death. Stimulation of the respiratory center seems to depend upon the character of the blood. If it is well oxygenized, the breathing is slow and quiet; if there is a lack of oxygen, dyspnœa results. Probably certain chemical substances in the blood, which are ordinarily rapidly burned up by the oxygen but [Pg 131] which accumulate in its absence, serve to stimulate the respiratory center, thus adjusting the effort to get oxygen to the need of it. Respiration may be stopped by stimulating the mucous membrane of the nose, as with strong ammonia.

Nervous Mechanism.—Respiration is controlled nervously in three ways: 1. by the phrenic nerve to the diaphragm; 2. by some fibers of the vagus or pneumogastric nerve, and 3. by the respiratory center in the bulbous part of the spinal cord. An injury to the respiratory center means that respiration stops and can lead to death. Stimulation of the respiratory center appears to depend on the condition of the blood. If the blood is well-oxygenated, breathing is slow and calm; if there’s a lack of oxygen, it causes difficulty in breathing. Certain chemical substances in the blood, which are normally quickly used up by oxygen but accumulate when oxygen is low, probably stimulate the respiratory center, helping to adjust the need for oxygen to match demand. Breathing can be halted by stimulating the mucous membrane of the nose, such as with strong ammonia.

Variations.—Certain variations from the ordinary respiration might be mentioned here. A deep inspiration followed by a long expiration is known as a sigh and a very deep inspiration through the mouth only as a yawn. Hiccough results from a sudden inspiratory contraction of the diaphragm during which the glottis is suddenly closed. In sobbing the inspirations are short and rapid with a prompt closing of the glottis between. Both coughing and sneezing consist of a deep inspiration followed by complete closure of the glottis and then its sudden opening and the forcible expulsion of air. Coughing, however, is generally caused by an irritation or obstruction of the larynx or trachea and the air is expelled through the mouth, while sneezing is caused by irritation of the nasal passages and the air is driven out through the nose. Laughing and crying also resemble one another in that each is an inspiration followed by a series of short, spasmodic expirations, during which the glottis is open and the vocal cords in characteristic vibration. They differ, however, in rhythm and in the facial expression that accompanies them.

Variations.—There are some variations from normal breathing worth mentioning. A deep inhale followed by a long exhale is called a sigh, while a very deep inhale through the mouth alone is a yawn. Hiccups occur when there’s a sudden contraction of the diaphragm that causes the glottis to close abruptly. In sobbing, the breaths are short and quick with a quick closure of the glottis in between. Both coughing and sneezing involve a deep inhale, a complete closure of the glottis, and then a sudden opening that forcefully expels air. Coughing is usually triggered by irritation or blockage in the larynx or trachea, with air expelled through the mouth, while sneezing is triggered by irritation in the nasal passages, pushing air out through the nose. Laughing and crying share similarities as each involves an inhale followed by a series of short, spasmodic exhales, during which the glottis remains open and the vocal cords vibrate in a distinctive way. They differ, however, in their rhythm and the facial expressions that come with them.


CHAPTER X.
THE ABDOMEN AND THE ORGANS
OF DIGESTION AND EXCRETION.

The Abdominal Cavity.—Below the diaphragm and separated from the lowest cavity of the trunk, the pelvis, only by an invisible plane drawn through the brim of the true pelvis, is the abdominal cavity, which may be said in a general way to contain the organs of digestion and the kidneys. It is protected behind by the vertebræ and anteriorly by the lower ribs above and below by muscular walls, which make possible the complete bending of the body. These muscles are for the most part large and very strong and the greater number are inserted, in part at least, into a median tendinous line, the linea alba, which passes from the ensiform cartilage of the sternum above to the symphysis pubis below.

The Abdominal Cavity.—Below the diaphragm and separated from the lowest part of the trunk, the pelvis, only by an invisible line drawn through the edge of the true pelvis, is the abdominal cavity, which generally contains the organs of digestion and the kidneys. It is protected in the back by the vertebrae and in the front by the lower ribs, while the abdominal muscles provide support above and below, allowing for full bending of the body. These muscles are mostly large and very strong, and most of them attach, at least partially, to a central tendinous line, the linea alba, which runs from the xiphoid process of the sternum above to the pubic symphysis below.

Muscles.—The external oblique muscles form the outermost layer of the abdominal wall. They rise from the external surface of the eight lower ribs on either side and are inserted in the anterior half of the iliac crest as well as by aponeurosis in the linea alba, where each joins its fellow from the opposite side, the fibers running downward and inward like the fingers in the trouser’s pocket. Along the lower border of the aponeurosis is a broad fold, Poupart’s ligament. The internal oblique rises on either side from the outer half of Poupart’s ligament and the anterior part of the crest of the ilium and is inserted into the crest of the os pubis, the cartilages of the lower ribs, and the linea alba. Its fibers run at right angles to those of the external oblique. These oblique muscles serve to compress the viscera, to flex the body, and also assist in expiration. [Pg 133]

Muscles.—The external oblique muscles make up the outermost layer of the abdominal wall. They extend from the external surface of the eight lower ribs on each side and connect to the anterior half of the iliac crest, as well as through aponeurosis in the linea alba, where they meet their counterparts from the opposite side, with the fibers running downward and inward like fingers in a trouser pocket. A broad fold, Poupart’s ligament, exists along the lower edge of the aponeurosis. The internal oblique originates on either side from the outer half of Poupart’s ligament and the front part of the iliac crest, inserting into the crest of the pubic bone, the cartilage of the lower ribs, and the linea alba. Its fibers run at right angles to those of the external oblique. These oblique muscles help to compress the internal organs, flex the body, and assist with exhaling. [Pg 133]

The deepest of the abdominal muscles is the transversalis, which rises from the outer third of Poupart’s ligament and the adjoining part of the crest of the ilium, from the six lower costal cartilages, and by a broad aponeurosis, the lumbar fascia, from the lumbar vertebræ. It is inserted into the pubic crest and by aponeurosis into the linea alba. There is one of these muscles on either side.

The innermost of the abdominal muscles is the transversalis, which originates from the outer third of Poupart’s ligament and the nearby part of the ilium crest, from the six lower rib cartilages, and through a broad connective tissue layer, the lumbar fascia, from the lumbar vertebrae. It attaches to the pubic crest and, through a connective tissue layer, to the linea alba. There is one of these muscles on each side.

Fig. 51.—Muscles of the trunk from before (left side, superficial; and right side, deep): 1, Pectoralis major; 2, deltoid; 3, portion of latissimus dorsi; 4, serratus magnus; 5, subclavius; 6, the pectoralis, sternocostal portion; 7, serratus magnus; 12, rectus abdominis; 13, internal oblique; 14, external oblique; 15, abdominal aponeurosis and tendinous intersections of rectus abdominis; 16, over symphysis pubis; 17, linea semilunaris; 18, gluteus medius; 19, tensor vaginæ femoris; 20, rectus femoris; 21, sartorius; 22, femoral part of iliopsoas; 23, pectineus; 24, adductor longus; 25, gracilis. (Dorland’s Dictionary.)

Fig. 51.—Muscles of the trunk from the front (left side, superficial; and right side, deep): 1, Pectoralis major; 2, deltoid; 3, part of latissimus dorsi; 4, serratus magnus; 5, subclavius; 6, the pectoralis, sternocostal part; 7, serratus magnus; 12, rectus abdominis; 13, internal oblique; 14, external oblique; 15, abdominal aponeurosis and tendinous intersections of rectus abdominis; 16, over symphysis pubis; 17, linea semilunaris; 18, gluteus medius; 19, tensor vaginæ femoris; 20, rectus femoris; 21, sartorius; 22, femoral part of iliopsoas; 23, pectineus; 24, adductor longus; 25, gracilis. (Dorland’s Dictionary.)

[Pg 134] The rectus abdominis is also really two muscles and extends from the symphysis pubis to the cartilages of the fifth, sixth, and seventh ribs. At first it passes back of the oblique and transversalis muscles, but about a fourth of the way up it passes in front of the transversalis and between two layers of the internal oblique, which thereafter forms its sheath. Its chief duty is to flex the chest on the pelvis, though it also compresses the abdominal viscera.

[Pg 134] The rectus abdominis is actually two muscles and runs from the pubic symphysis to the cartilage of the fifth, sixth, and seventh ribs. Initially, it goes behind the oblique and transversalis muscles, but about a quarter of the way up, it moves in front of the transversalis and between two layers of the internal oblique, which then forms its sheath. Its main function is to flex the chest towards the pelvis, although it also helps compress the abdominal organs.

One other muscle, a small one, is found in front, the pyramidalis, which rises from the pubic crest and is inserted into the linea alba midway to the umbilicus.

One more muscle, a small one, is located in the front, the pyramidalis, which originates from the pubic crest and attaches to the linea alba halfway to the belly button.

At the back the open space over the kidneys, between the lower ribs and the os innominatum, is closed in on either side by the quadratus lumborum, which extends from the three or four lower lumbar vertebræ and the adjacent iliac crest to the last rib and the upper four lumbar vertebræ. It flexes the trunk laterally or forward according as one muscle or both are used, and may aid in either expiration or inspiration.

At the back, the open area over the kidneys, between the lower ribs and the hip bone, is bordered on each side by the quadratus lumborum, which stretches from the three or four lower lumbar vertebrae and the nearby iliac crest to the last rib and the upper four lumbar vertebrae. It bends the trunk to the side or forward depending on whether one muscle or both are in use, and it can assist with either exhaling or inhaling.

The nerves of the abdominal muscles are chiefly the internal intercostals.

The nerves of the abdominal muscles mainly come from the internal intercostals.

The Peritoneum.—Lining the abdominal cavity is a serous membrane, the peritoneum, which is reflected back over the viscera within in such a way as to cover each one wholly or in part. Folds of peritoneum, the omenta, connect the stomach with the other viscera, the most important being the great omentum, which has one layer descending from the anterior and another from the posterior wall of the stomach. The mesenteries are double layers of peritoneum which hold the intestines to the vertebræ and posterior wall. Between their folds run the blood-vessels.

The Peritoneum.—The abdominal cavity is lined with a serous membrane called the peritoneum, which wraps around the organs inside, covering each one completely or partially. The folds of peritoneum, known as the omenta, connect the stomach to the other organs, with the most significant being the great omentum, which has one layer coming down from the front and another from the back wall of the stomach. The mesenteries are double layers of peritoneum that anchor the intestines to the spine and back wall. Blood vessels run between their folds.

Fig. 52.—Diagram showing the nine regions of the abdominal cavity: 1, Right hypochondriac; 2, epigastric; 3, left hypochondriac; 4, right lumbar; 5, umbilical; 6, left lumbar; 7, right iliac; 8, hypogastric; 9, left iliac. (Ashton.)

Fig. 52.—Diagram showing the nine areas of the abdominal cavity: 1, Right hypochondriac; 2, epigastric; 3, Left hypochondriac; 4, Right lumbar; 5, Umbilical; 6, Left lumbar; 7, Right iliac; 8, Hypogastric; 9, Left iliac. (Ashton.)

Abdominal Regions.—For convenience of description the abdominal cavity has been divided into nine regions by means of two transverse parallel lines, the one through the ninth costal cartilages and the other just over the iliac crests, and two perpendicular parallel lines [Pg 135] through the cartilage of the eighth rib and the middle of Poupart’s ligament on either side. These nine regions have been named as follows: The right and left hypochondriac regions up under the ribs with the epigastrium between, the right and left lumbar regions next below with the umbilical between, and the right and left inguinal with the hypogastric between. Others divide it into quadrants by one line drawn across and another down through the umbilicus. The contents of the abdomen in full are the stomach, intestines, liver, gall-bladder, spleen, pancreas, kidneys, suprarenal capsules, and the great vessels, [Pg 136] that is, the organs of digestion and excretion. When distended the bladder extends up into the abdominal cavity, as does the uterus also when enlarged.

Abdominal Regions.—To make it easier to describe, the abdominal cavity is divided into nine regions using two parallel horizontal lines: one at the level of the ninth costal cartilages and the other just above the iliac crests, along with two vertical parallel lines through the cartilage of the eighth rib and the middle of Poupart’s ligament on each side. These nine regions are named as follows: the right and left hypochondriac regions under the ribs with the epigastrium in between, the right and left lumbar regions just below that with the umbilical in between, and the right and left inguinal with the hypogastric in between. Some people divide it into quadrants using one line across and another down through the umbilicus. The full contents of the abdomen include the stomach, intestines, liver, gall-bladder, spleen, pancreas, kidneys, adrenal glands, and major blood vessels, which are the organs involved in digestion and excretion. When full, the bladder expands into the abdominal cavity, as does the uterus when it is enlarged.

Salivary Digestion.—Although most of the digestive organs are situated in the abdomen, the food enters the body through the mouth, where its prehension is a voluntary act. Here digestion also begins and from the first the process is a double one, mechanical and chemical, mechanical digestion consisting largely of muscular movements by which the food is ground up and carried through the digestive tract. Thorough mastication or grinding of the food by the teeth is necessary, while the tongue assists by moving the food about and by mixing it thoroughly with the saliva, a viscid fluid composed of water and salts and having a slightly alkaline reaction. The saliva is secreted by the parotid, sublingual, and submaxillary glands, and serves to soften and dissolve the food and by virtue of its unorganized ferment, ptyalin, to convert starch into sugar. Upon proteins and fats it has practically no digestive action. Moderate warmth and an alkaline medium favor its action, while extremes of heat or cold or an acid medium hinder it. There is little absorption in the mouth, though starch, nicotine, and alcohol may be absorbed in small quantities.

Salivary Digestion.—Even though most of the digestive organs are located in the abdomen, food enters the body through the mouth, where the act of eating is voluntary. Digestion also starts here, and from the beginning, it's a two-part process: mechanical and chemical. Mechanical digestion relies mainly on muscle movements that grind up the food and push it through the digestive tract. It's important to chew the food thoroughly with the teeth, while the tongue helps by moving the food around and mixing it well with the saliva, a sticky fluid made of water and salts that is slightly alkaline. The saliva is produced by the parotid, sublingual, and submaxillary glands, and it helps to soften and dissolve the food. Thanks to its unorganized enzyme, ptyalin, it also converts starch into sugar. It has almost no digestive effect on proteins and fats. Moderate warmth and an alkaline environment promote its action, while extreme heat or cold or an acidic environment impede it. There is minimal absorption in the mouth, although small amounts of starch, nicotine, and alcohol can be absorbed.

The Pharynx.—When the food is ready for deglutition or swallowing, it is thrust back into the pharynx, a somewhat conical, musculo-membranous sac, situated, base upward, behind the nose and mouth and behind, but somewhat above, the larynx. The pharynx is about four and a half inches long and ends on a level with the cricoid cartilage in the esophagus or gullet. It is attached to the vertebræ at the back and opens in front into the mouth. The posterior nares, the Eustachian tubes, and the larynx also open into it, the last being protected by the epiglottis, which closes during deglutition to prevent food from entering the air passages, just as the soft palate is drawn back to prevent regurgitation of food into the nose. There are [Pg 137] three coats to the pharynx: 1. a mucous coat continuous with that of the mouth and ciliated down to the floor of the nares; 2. a fibrous coat, and 3. a muscular coat containing among others the constrictor muscles which serve to carry the food down to the esophagus. Its arteries are branches of the external carotid and its nerves come from the spinal accessory and the sympathetic. Occasionally a foreign body gets lodged in the pharynx just out of reach of the finger and threatens strangulation. Retropharyngeal abscess on the posterior wall occurs rarely.

The Pharynx.—When food is ready to be swallowed, it gets pushed back into the pharynx, which is a somewhat cone-shaped, muscle-and-membrane sac located behind the nose and mouth, and slightly above the larynx. The pharynx is about four and a half inches long and connects to the esophagus, or gullet, at the level of the cricoid cartilage. It's attached to the vertebrae at the back and opens at the front into the mouth. The posterior nares, Eustachian tubes, and larynx also open into it, with the larynx protected by the epiglottis, which closes during swallowing to stop food from entering the air passages, while the soft palate moves back to prevent food from going up into the nose. There are [Pg 137] three layers to the pharynx: 1. a mucous layer that connects with the mouth and is lined with cilia down to the floor of the nares; 2. a fibrous layer, and 3. a muscular layer that includes the constrictor muscles, which help push food down to the esophagus. Its arteries come from the external carotid, and its nerves originate from the spinal accessory and sympathetic nervous systems. Occasionally, a foreign body can get stuck in the pharynx, just out of reach of the fingers, potentially causing strangulation. A retropharyngeal abscess on the back wall is rare.

Fig. 53.—Position of the thoracic and abdominal organs,
front view. (Morrow.)

Fig. 53.—Position of the thoracic and abdominal organs,
front view. (Morrow.)

[Pg 138] The Esophagus.—From the pharynx the food passes to the cardiac orifice of the stomach, opposite the tenth dorsal vertebra, through the esophagus, a muscular tube about nine inches long, which collapses when empty, its lumen then appearing as a transverse slit. It, too, has three coats: 1. an inner mucous coat; 2. an areolar coat, and 3. a muscular coat, the muscles being arranged in two sets, an outer longitudinal layer and an inner circular layer. By a series of rhythmic contractions, especially of the circular fibers, the food is pushed along, though sometimes with liquid food there is no peristaltic action of the esophagus, the pharyngeal muscles alone sending it to the stomach. At the lower end of the esophagus an especially strong band of circular muscle fibers form a sort of sphincter, which prevents the regurgitation of food. The whole act of swallowing is a reflex, not a voluntary act and is due to irritation set up by the stimulus of the foreign body, the food. Stricture of the esophagus is common and may be of three kinds: 1. spasmodic, occurring in nervous women; 2. fibrous, due to scar tissue, or 3. malignant, due to cancer.

[Pg 138] The Esophagus.—From the throat, food travels to the opening of the stomach, opposite the tenth dorsal vertebra, through the esophagus, a muscular tube about nine inches long that collapses when empty, making its opening look like a transverse slit. It also has three layers: 1. an inner mucous layer; 2. an areolar layer; and 3. a muscular layer, with muscles arranged in two sets: an outer longitudinal layer and an inner circular layer. Through a series of rhythmic contractions, particularly of the circular fibers, food is pushed along. However, with liquids, there might not be any peristaltic action in the esophagus; the muscles of the throat may solely move it to the stomach. At the lower end of the esophagus, a strong band of circular muscle fibers forms a kind of sphincter that prevents food from coming back up. The entire swallowing process is a reflex, not something we do voluntarily, and is triggered by the irritation caused by the presence of the food. Stricture of the esophagus is common and can be of three types: 1. spasmodic, which occurs in nervous women; 2. fibrous, caused by scar tissue; or 3. malignant, resulting from cancer.

The Stomach.The stomach is a pear-shaped dilatation of the alimentary canal, lying under the liver and diaphragm in the epigastrium and left hypochondrium and connecting the esophagus with the small intestine. It lies largely behind the ribs, but the greater curvature is only two fingers’ breadth above the umbilicus and can be manipulated through the skin. The cardiac end, into which the esophagus enters, is the larger and points upward to the left. The lesser and lower end, known as the pylorus, is at the right and its opening into the small intestine is guarded by the pyloric sphincter. The lesser curvature is concave and on the upper surface; the greater, convex and on the under surface. The great omentum is attached to the latter.

The Stomach.The stomach is a pear-shaped enlargement of the digestive tract, located beneath the liver and diaphragm in the upper abdomen and left side, connecting the esophagus with the small intestine. It mainly sits behind the ribs, but the greater curvature is only about two finger widths above the belly button and can be felt through the skin. The cardiac end, where the esophagus enters, is larger and points up and to the left. The smaller and lower end, called the pylorus, is on the right, and its opening into the small intestine is regulated by the pyloric sphincter. The lesser curvature is curved inward on the top surface, while the greater curvature is rounded and on the underside. The great omentum is attached to the greater curvature.

In size the stomach varies more or less, that of a man generally being larger than that of a woman, but it is usually about ten inches [Pg 139] long and four or five inches across. It has a capacity of about five pints and serves as a storehouse for food.

In size, the stomach varies, with men's stomachs generally being larger than women's, but it's usually around ten inches long and four or five inches wide. It can hold about five pints and acts as a storage area for food. [Pg 139]

The stomach has four coats: 1. a serous coat derived from the peritoneum; 2. a muscular coat of three layers with longitudinal fibers continuous with those of the esophagus, circular fibers, and oblique fibers; 3. an areolar coat, and 4. a mucous coat, which, when the stomach is empty, is thrown into longitudinal folds or rugæ, and whose surface is covered with glands, the gastric glands, for the secretion of the digestive fluids.

The stomach has four layers: 1. a serous layer that comes from the peritoneum; 2. a muscular layer made up of three layers with longitudinal fibers that connect to those of the esophagus, circular fibers, and oblique fibers; 3. an areolar layer; and 4. a mucous layer, which, when the stomach is empty, is folded into long ridges or folds called rugæ, and its surface is lined with glands, known as gastric glands, that secrete digestive fluids.

The arteries come from the celiac axis and the nerves from the pneumogastric and the solar plexus.

The arteries originate from the celiac axis, and the nerves come from the vagus nerve and the solar plexus.

Ulcer and cancer of the stomach are both rather common. In the former there is apt to be hyper-acidity and in the latter hypo-acidity, but the rule does not always hold. In cases of ulcer there may be hemorrhage and even perforation. Such hemorrhage can be distinguished from hemorrhage from the lungs by its slightly acid odor and by the frothy character of hemorrhage from the lungs. There is much irritation at the pylorus and where there is irritation there is liable to be cancer.

Stomach ulcers and cancer are both quite common. With ulcers, there's often hyper-acidity, while with cancer, there tends to be hypo-acidity, though this isn't always the case. In ulcer cases, there can be bleeding and even perforation. This bleeding can be differentiated from that caused by lung issues by its slightly acidic smell and the frothy appearance of lung-related bleeding. There's a lot of irritation at the pylorus, and where there's irritation, cancer is likely to develop.

Gastric Digestion.—In the stomach the food is churned and thoroughly mixed with the gastric juices, and it is also subjected to a propulsive movement that drives it on to the intestine. When it comes to the stomach it is semi-solid and when it has become fluid or semi-fluid, in which state it is known as chyme, it is ready to pass on. Before it can do so, however, it must overcome the strong pyloric sphincter, and this it does by the muscles about the sphincter pushing it constantly on until the sphincter gives way. Probably most of the propulsive movements take place within a few inches of the pylorus.

Gastric Digestion.—In the stomach, food is mixed and churned thoroughly with gastric juices, and it also experiences movements that push it into the intestine. When food enters the stomach, it is semi-solid, and once it becomes liquid or semi-liquid, it's known as chyme, which is when it’s ready to move on. However, before it can do that, it has to get past the strong pyloric sphincter, and it achieves this by the muscles around the sphincter pushing it continuously until the sphincter opens. Most of the propulsive movements likely occur within a few inches of the pylorus.

The gastric juice is secreted by glands in the wall of the stomach and poured out through little tubules which project from the surface. It is a thin, almost colorless fluid with a sour taste and odor due to the presence of free hydrochloric acid, an important element in digestion. Probably when the stomach is empty and for some twenty [Pg 140] minutes after the appearance of food there is no hydrochloric acid present and, the food being alkaline, salivary digestion continues. Then, called forth by the presence of the food, the hydrochloric acid appears and salivary digestion ceases in the acid medium. Little digestion of starches or fats takes place, the chief action being on proteins, which are converted into soluble peptones. For besides hydrochloric acid the gastric juice contains two ferments: 1. pepsin, which is particularly active in aiding the digestion of proteins, and 2. rennin, which especially affects milk. Neither hydrochloric acid nor pepsin seems capable of digesting food alone, but each is essential to the other. They are secreted by different types of cells, secretion depending upon the nerve supply and upon the presence of food. Gastric digestion is favored by minute subdivision of the food and by the right proportion of hydrochloric acid, which should be 0.2 per cent. Body temperature is also advantageous. Except that proteins are put in solution and partly digested, little digestion goes on in the stomach, and though the rugæ afford a large absorbing surface, little absorption takes place, although more takes place than in the mouth and in time most foods, except fats, can be absorbed. The time of digestion varies with different foods and in different people, but probably three to five hours are necessary. The food leaves the stomach as chyme, a fluid of about the consistency of pea soup.

The gastric juice is produced by glands in the stomach wall and released through small tubules that stick out from the surface. It’s a thin, almost colorless fluid with a sour taste and smell due to the free hydrochloric acid, which is a key part of digestion. When the stomach is empty and for about twenty [Pg 140] minutes after food appears, there is no hydrochloric acid present, and since the food is alkaline, salivary digestion keeps going. Then, triggered by the food, the hydrochloric acid shows up and salivary digestion stops in the acidic environment. Little digestion of starches or fats happens; the main process works on proteins, which get turned into soluble peptones. Besides hydrochloric acid, gastric juice contains two enzymes: 1. pepsin, which is especially important for breaking down proteins, and 2. rennin, which mainly affects milk. Neither hydrochloric acid nor pepsin can digest food on their own, but each is crucial for the other. They’re secreted by different types of cells, and this secretion depends on nerve signals and the presence of food. Gastric digestion is helped by breaking food into small pieces and having the right amount of hydrochloric acid, which should be 0.2 percent. Body temperature also helps. Except for proteins being dissolved and partially digested, not much digestion occurs in the stomach, and although the rugæ provide a large surface area for absorption, only a little absorption happens—though it is still more than in the mouth, and over time most foods, except fats, can be absorbed. The time it takes to digest varies with different foods and among different people, but it typically takes three to five hours. The food leaves the stomach as chyme, a fluid with a consistency similar to pea soup.

Vomiting is more or less the reverse of swallowing and is generally preceded by a feeling of nausea, which starts up retching, a more or less involuntary effort of the stomach to throw off its contents. To relieve the retching a long breath is taken, followed by a deep expiration that opens the cardiac end of the stomach and allows the abdominal muscles to force the food out. After much vomiting and prolonged retching the pyloric end of the stomach may be affected and bile will then appear in the vomitus. Artificial vomiting may be [Pg 141] produced by irritation of the gastric nerve center in the brain or by irritation of the stomach itself.

Vomiting is basically the opposite of swallowing and usually starts with a feeling of nausea, which triggers retching, an involuntary response of the stomach to expel its contents. To ease the retching, a deep breath is taken, followed by a strong exhale that opens the entrance to the stomach and helps the abdominal muscles push the food out. After a lot of vomiting and extended retching, the end of the stomach may be affected, causing bile to appear in the vomit. Artificial vomiting may be [Pg 141] induced by irritating the gastric nerve center in the brain or by irritating the stomach itself.

Fig. 54.—The intestinal canal: 1, Stomach; 2, duodenum; 3, jejunum; 4, ileum; 5, cecum; 6, vermiform appendix; 7, ascending colon; 8, transverse colon; 9, descending colon; 10, sigmoid flexure; 11, rectum. (Leidy.)

Fig. 54.—The intestinal canal: 1, Stomach; 2, duodenum; 3, jejunum; 4, ileum; 5, cecum; 6, vermiform appendix; 7, ascending colon; 8, transverse colon; 9, descending colon; 10, sigmoid flexure; 11, rectum. (Leidy.)

Intestinal Canal.—From the stomach the food passes into the intestinal canal, a convoluted tube which extends from the stomach to the anus and in which, more particularly in the upper portion, the greater part of the digestion and absorption of food takes place. This tube, which is about six times the height of its possessor, consists of two parts, the small and the large intestines, the first four-fifths, or about 25 feet, being small intestine. It occupies the central and lower parts of the abdominal cavity and a small portion of the pelvic cavity, and is attached to the spine by the mesentery, which, however, [Pg 142] allows great freedom of motion, so that there is little fixation to the loops of the small intestines.

Intestinal Canal.—From the stomach, food moves into the intestinal canal, a twisted tube that stretches from the stomach to the anus, where a significant portion of digestion and nutrient absorption occurs, especially in the upper part. This tube is about six times the height of the person it belongs to and has two main sections: the small and large intestines. The small intestine makes up the first four-fifths, which is roughly 25 feet long. It fills the central and lower areas of the abdominal cavity and a small part of the pelvic cavity, and it is connected to the spine by the mesentery, which allows for considerable movement, resulting in minimal fixation of the small intestine loops. [Pg 142]

The Small Intestine.—The small intestine opens out of the stomach and has three divisions: 1. the duodenum, which is only about ten to twelve inches long; 2. the jejunum, so called because it is generally empty after death, which is about two-fifths of the remainder and lies chiefly in the umbilical region and the left iliac fossa, and 3. the ileum or curved intestine, the remaining three-fifths, which gets its name from its numerous coils and which lies in the middle and the right side of the abdomen. There is no direct division between the jejunum and the ileum, but the first part of the former and the last part of the latter are quite different in character. At its entrance into the large intestine the ileum is guarded by the ileo-cecal valve.

The Small Intestine.—The small intestine connects to the stomach and has three sections: 1. the duodenum, which is about ten to twelve inches long; 2. the jejunum, named because it is usually empty after death, which makes up about two-fifths of the remaining length and is primarily located in the belly button area and the left side of the pelvis, and 3. the ileum or curved intestine, which accounts for the remaining three-fifths, named for its many coils and located in the middle and right side of the abdomen. There's no clear separation between the jejunum and the ileum, but the first part of the jejunum and the last part of the ileum have distinct characteristics. At its connection to the large intestine, the ileum is protected by the ileo-cecal valve.

Fig. 55.
1, Central lacteal;  
2, capillary network;
3, columnar cells.  

Fig. 55.
1, Central lacteal;  
2, capillary network;
3, columnar cells.

The same coats continue in the small intestine as were found in the stomach, but they are here much thinner and the inner coat is shaggy, like velvet, with innumerable minute processes called villi, which greatly increase the absorbing surface. In fact, the great length of the intestine as well as the presence of the villi is aimed to provide a large surface to absorb the food as it passes, an even greater increase of surface being provided by the fact that the intestinal wall is thrown into folds, the valvulæ conniventes. Each villus is covered with a layer of columnar epithelial cells and has within connective tissue, in which are found a fine capillary network and open lymph spaces from which leads a single lacteal vessel.

The same coats that are found in the stomach continue in the small intestine, but they’re much thinner here. The inner coat is shaggy and soft, like velvet, covered in countless tiny projections called villi, which greatly increase the surface area for absorption. In fact, the long length of the intestine and the presence of the villi are designed to provide a large surface for absorbing food as it moves through. There’s also a further increase in surface area because the intestinal wall has folds, known as valvulæ conniventes. Each villus is topped with a layer of columnar epithelial cells and contains connective tissue, which houses a fine network of capillaries and open lymph spaces leading to a single lacteal vessel.

Closely connected with the lymphatic vessels are the solitary glands, small round bodies the size of a small pin’s head. Peyer’s glands or patches are patches of solitary glands opposite the mesenteric attachment and are largest and most numerous in the ileum. In typhoid [Pg 143] fever they are involved and may become the seat of ulcers. There are also the glands of Lieberkühn which secrete the succus entericus.

Closely connected with the lymphatic vessels are the solitary glands, small round bodies about the size of a small pin’s head. Peyer’s glands or patches are clusters of solitary glands located opposite the mesenteric attachment and are largest and most numerous in the ileum. In typhoid [Pg 143] fever, they are affected and may develop ulcers. There are also the glands of Lieberkühn, which secrete the succus entericus.

The arteries of the small intestine, which include the superior mesenteric, are from the celiac axis and the nerves are from the superior mesenteric plexus of the sympathetic. The veins empty chiefly into the portal system.

The arteries of the small intestine, including the superior mesenteric, branch from the celiac axis, while the nerves originate from the sympathetic superior mesenteric plexus. The veins primarily drain into the portal system.

The movements of the intestine, like those of the esophagus, are peristaltic, but the action is complicated by the fact that the tube is not straight but in coils.

The movements of the intestine, like those of the esophagus, are peristaltic, but the action is complicated by the fact that the tube is not straight but coiled.

Intestinal Digestion.—The food, which enters the duodenum as chyme, there comes in contact with the bile and the pancreatic juice, which together but unmixed enter the duodenum from their respective ducts by a common orifice. As in the stomach, the digestive juices are called forth by the presence of food. The bile is secreted in the liver, from which it flows away through the hepatic duct, which joins the cystic duct from the gall-bladder to form the common bile duct. Through this it flows into the intestine during digestion, but between whiles it passes up into the gall-bladder, where it is stored for future use and whence it is expelled when needed. When pure it is a thick, viscid liquid, varying from a bright red to a greenish-yellow in color according to the pigments present, and of an alkaline reaction. It consists chiefly of the bile pigments, biliverdin, which gives the green color, and bilirubin, which gives the red color, and of bile salts in solution, cholesterin, which probably forms the basis of many gall stones, is also present. Bile is a disinfectant to the bowel and a lubricant for the feces. How much digestive action it has is a question, but it affords the necessary alkaline medium for the pancreatic juice to act in.

Intestinal Digestion.—The food, which enters the duodenum as chyme, comes into contact with bile and pancreatic juice, which enter the duodenum from their respective ducts through a shared opening. Just like in the stomach, the presence of food triggers the production of digestive juices. The bile is produced in the liver, where it flows through the hepatic duct, joining the cystic duct from the gallbladder to form the common bile duct. During digestion, bile flows into the intestine, but at other times, it goes back into the gallbladder, where it is stored for later use and released when needed. When pure, it is a thick, sticky liquid that can range from bright red to greenish-yellow, depending on the pigments present, and has an alkaline nature. It mainly consists of bile pigments, biliverdin, which gives it the green color, and bilirubin, responsible for the red color, along with bile salts in solution. Cholesterin, which likely forms the basis of many gallstones, is also present. Bile acts as a disinfectant for the bowel and a lubricant for feces. Its effectiveness in digestion is debated, but it provides the necessary alkaline environment for pancreatic juice to function.

The pancreatic juice is secreted by the pancreas, from which it enters the intestine through the pancreatic duct, and is probably the most important fluid in the digestive process. It is clear, practically colorless, slightly viscid or gelatinous, and quite strongly alkaline in reaction, owing to the presence of sodium carbonate. It contains [Pg 144] three ferments, amylopsin for the digestion of starch, trypsin for the digestion of proteins, and steapsin for the digestion of fats. By it, as by the saliva, starch is turned into sugar or maltose, in which form it is absorbed, while proteins are converted into peptones, as they are in the stomach. Since, however, fats are acted on nowhere else, the chief function of the pancreatic juice may be considered to be the digestion of fats. Having broken through their albuminous envelope, it divides them into glycerine and fatty acids and then emulsifies them with the assistance of the bile.

The pancreatic juice is produced by the pancreas, and it enters the intestine through the pancreatic duct. It is likely the most crucial fluid in the digestive process. It is clear, nearly colorless, slightly thick or gelatinous, and very alkaline due to the presence of sodium carbonate. It contains [Pg 144] three enzymes: amylopsin for starch digestion, trypsin for protein digestion, and steapsin for fat digestion. Similar to saliva, it converts starch into sugar or maltose, which is then absorbed, while proteins are transformed into peptones, as they are in the stomach. However, since fats are not processed anywhere else, the primary role of pancreatic juice can be seen as the digestion of fats. It breaks through their protein coating, separates them into glycerine and fatty acids, and then emulsifies them with the help of bile.

The food also comes in contact with the succus entericus, a juice secreted by the glands of Lieberkühn in the small intestine, whose chief action is the conversion of sugar into glucose.

The food also comes in contact with the succus entericus, a juice secreted by the Lieberkühn glands in the small intestine, whose main function is to convert sugar into glucose.

Absorption.—As the food is absorbed from the intestine it is liquid and entirely digested and is known as chyle. Practically all absorption takes place from the small intestine, though there is a little in the large intestine. It takes place in two ways: 1. through the portal vessels and 2. through the lacteals, which are the lymphatic vessels of the small intestine. Fats are absorbed practically entirely by the lacteals. They enter the cells covering the villi, travel thence to the lymph spaces, and so into the lacteal or main lymph channel, whence they are carried to the thoracic duct and the general circulation. From the blood they are absorbed as fat and stored up as adipose or fatty tissue, which is found throughout the body in connective tissue about the organs. Organic salts and water are for the most part absorbed by the portal system, which they reach through the capillaries of the villi and through which they go to the liver. Starches, in the form of sugar, pass between the cells of the villi into the lymph spaces, from which they are taken up by the capillaries. On the way to the liver maltose becomes dextrose. Proteins, in the form of peptones, pass through the layer of epithelial cells to the lymph [Pg 145] spaces and then to the capillaries, an active part being taken by the cells. By the time they reach the liver the peptones have been changed back into proteins. In fact, peptones seem to have some poisonous effect upon the blood if they get into it as such.

Absorption.—When food is absorbed from the intestine, it is liquid and fully digested, known as chyle. Most of the absorption occurs in the small intestine, although a small amount takes place in the large intestine. This happens in two ways: 1. through the portal vessels and 2. through the lacteals, which are the lymphatic vessels of the small intestine. Fats are almost entirely absorbed by the lacteals. They enter the cells that line the villi, move on to the lymph spaces, and then into the lacteal or main lymph channel, from where they are transported to the thoracic duct and into the general circulation. From the blood, they are absorbed as fat and stored as adipose or fatty tissue, found throughout the body in connective tissue around the organs. Organic salts and water are mainly absorbed by the portal system, which they reach through the capillaries of the villi and through which they go to the liver. Starches, in the form of sugar, pass between the cells of the villi into the lymph spaces, from which they are absorbed by the capillaries. On the way to the liver, maltose converts to dextrose. Proteins, in the form of peptones, travel through the layer of epithelial cells to the lymph [Pg 145] spaces and then to the capillaries, with the cells playing an active role. By the time they reach the liver, the peptones have been converted back to proteins. In fact, peptones seem to have a toxic effect on the blood if they enter it in their original form.

The Large Intestine.—The large intestine differs from the small in size and in fixity of position, lying curved in horseshoe shape above and around the small intestine. It is five or six feet long, large in caliber, and is thrown into crosswise folds. It has the same four coats as the small intestine, but the mucous coat is pale and smooth, without villi. Its glands are the crypts of Lieberkühn and the solitary glands. The arteries are branches of the superior and inferior mesenteric and the nerves come from sympathetic plexuses.

The Large Intestine.—The large intestine is different from the small intestine in size and in how it stays in place, curving in a horseshoe shape above and around the small intestine. It measures about five or six feet long, is wider in diameter, and has crosswise folds. It has the same four coats as the small intestine, but the mucous coat is pale and smooth, lacking villi. Its glands include the crypts of Lieberkühn and solitary glands. The arteries are branches from the superior and inferior mesenteric arteries, and the nerves come from sympathetic plexuses.

The blind sac lying in the right iliac fossa, with which the large intestine begins, is called the cecum, and into this the ileum opens, the ileo-cecal valve preventing regurgitation. Just below the ileo-cecal opening is the vermiform appendix, a narrow, worm-like tube with a blind end, varying in length from one to nine inches, but generally about four and one-half inches long, which, so far as is known, is functionless as well as dangerous. People have been born without an appendix and it has in rare instances grown again after operation. Its base is located in the living by McBurney’s point, a point two inches from the anterior superior spine of the ilium on a line drawn from the spine to the umbilicus.

The blind pouch located in the lower right abdomen, where the large intestine starts, is called the cecum, and the ileum connects to this pouch, with the ileo-cecal valve stopping anything from flowing back. Just below the ileo-cecal opening is the vermiform appendix, a thin, worm-shaped tube with a closed end, varying in length from one to nine inches, but typically around four and a half inches long, which, as far as we know, has no function and can be dangerous. Some people are born without an appendix, and in rare cases, it has regrown after surgery. Its base is found in the living at McBurney’s point, which is located two inches from the anterior superior spine of the ilium along a line drawn from the spine to the belly button.

From the cecum the intestine ascends in what is known as the ascending colon along the abdominal wall at the right to the under surface of the liver, where it turns in the hepatic flexure abruptly across the body to the left, passing below the liver, stomach, and spleen in the transverse colon. In the splenic flexure it turns down the left abdominal wall, the descending colon passing to the crest of the ilium, where there is another curve, the sigmoid flexure, leading to the rectum, which passes for six or eight inches down along the [Pg 146] vertebræ, a little to the left, to the anus, the external opening. This opening is guarded by two sphincter muscles, about an inch apart, the internal and external sphincters. The coils of the small intestine lie below the transverse colon, covered mostly by the omentum. The splenic flexure is behind the stomach and below the spleen and is slightly higher than the hepatic flexure. The sigmoid flexure can be felt in the left inguinal region in thin people.

From the cecum, the intestine rises in what is called the ascending colon along the right side of the abdominal wall to the underside of the liver, where it sharply bends at the hepatic flexure and crosses the body to the left, passing underneath the liver, stomach, and spleen in the transverse colon. At the splenic flexure, it curves down along the left abdominal wall, with the descending colon leading to the crest of the ilium, where there's another bend, the sigmoid flexure, which leads to the rectum, extending six to eight inches down along the [Pg 146] vertebrae, slightly to the left, to the anus, the external opening. This opening is protected by two sphincter muscles, about an inch apart, known as the internal and external sphincters. The loops of the small intestine are located beneath the transverse colon, mostly covered by the omentum. The splenic flexure is located behind the stomach and beneath the spleen and is slightly higher than the hepatic flexure. The sigmoid flexure can be felt in the left inguinal region in slim individuals.

The fact that the rectum is somewhat to the left is of importance in childbirth because if the rectum is packed, it may turn the child’s head in the wrong direction.

The fact that the rectum is slightly to the left is important during childbirth because if the rectum is full, it may cause the baby's head to turn in the wrong direction.

No digestion goes on in the large intestine, the function being to dry by absorbing water. The movements are practically the same as those of the small intestine except that they are much less active. Fermentation makes the contents acid. By the time food reaches the rectum it has been thoroughly digested and has given up its nourishment. It is then expelled as waste matter or feces. Defecation combines the involuntary movements of peristalsis and relaxation of the sphincters with the voluntary aid of the abdominal muscles. The ano-spinal reflex, by which movements of the bowel are regulated, is in the lumbar enlargement of the cord.

No digestion happens in the large intestine; its job is to dry out the contents by absorbing water. The movements are pretty much the same as those in the small intestine, though they are much less vigorous. Fermentation makes the contents acidic. By the time food reaches the rectum, it has been completely digested and has released its nutrients. It is then expelled as waste or feces. Defecation involves the involuntary actions of peristalsis and the relaxation of the sphincters, along with the voluntary help of the abdominal muscles. The ano-spinal reflex, which regulates bowel movements, is located in the lumbar enlargement of the spinal cord.

The hemorrhoidal veins in the lower rectum are connected with both the systemic and the portal veins and have no valves so that, as they are subjected to much strain, they often become varicose and dilated. This condition is called hemorrhoids or piles. Obstruction of the intestine may be caused by the growth of a constricting band, by intussusception or telescoping of the intestine on itself, especially at the ileo-cecal valve, or by volvulus or twisting. Foreign bodies are sometimes found in the appendix but they are not usually the cause of appendicitis. Cancer of the intestine is common and its mass is apt to cause obstruction with all its attendant symptoms. It may necessitate an artificial anus. Hernia or rupture may also occur and the hernia may become strangulated. [Pg 147]

The hemorrhoidal veins in the lower rectum are connected to both the systemic and portal veins and lack valves, so they often become varicose and dilated when stressed. This condition is known as hemorrhoids or piles. Obstruction of the intestine can occur due to the growth of a constricting band, intussusception (the intestine folding in on itself, especially at the ileo-cecal valve), or volvulus (twisting). Foreign bodies can sometimes be found in the appendix, but they typically aren't the cause of appendicitis. Cancer of the intestine is common, and its mass can lead to obstruction with all the associated symptoms. It might require the creation of an artificial anus. Hernia or rupture may also happen, and the hernia can become strangulated. [Pg 147]

Food and Metabolism.—Anything serves as food that replaces or hinders the loss to which the component parts of the body are liable. Proteins, carbohydrates, fats, some mineral matters, as salt and perhaps iron, and water are needed. The energy once expended by plants or animals in the formation of the materials which serve as food is set free in the body by the breaking up of these complex substances into their original elements, which are then recombined into the complex materials needed for the body’s life and growth. This process of building up complex materials from simple ones is known as anabolism and that of breaking them down as katabolism, while the two combined form the complete cycle of metabolism. Those foods have the best value that give up their energy most readily. For their combustion, heat, oxygen, and water are needed. Hunger indicates that the supply of material for katabolism has been used up and that more is needed, just as thirst indicates the need of the system for more fluids.

Food and Metabolism.—Anything that replaces or reduces the loss of the body's components serves as food. Proteins, carbohydrates, fats, certain minerals like salt and possibly iron, and water are essential. The energy that plants or animals originally used to create the materials that serve as food is released in the body when these complex substances break down into their basic elements, which are then reassembled into the complex materials necessary for the body’s life and growth. This process of building complex materials from simple ones is called anabolism, while the breakdown process is referred to as katabolism, and together they make up the complete cycle of metabolism. Foods that readily release their energy are considered the most valuable. Their combustion requires heat, oxygen, and water. Hunger signals that the supply of materials for katabolism has been depleted and that more is needed, just as thirst signifies the body’s need for more fluids.

The proteins or nitrogenous foods include all animal foods except fats, fish, crustaceans, eggs, milk and its products, certain vegetables, especially the lentils, that is, peas and beans, and gelatine. The fats include various fats and oils commonly eaten. The carbohydrates are the starchy foods, as cereals, sugars, fruits, and most vegetables, in fact, practically all except the lentils. Various beverages and condiments have no great nutritive value but serve to stimulate the appetite and to excite the secretion of the digestive juices. Coffee, tea, and alcohol are stimulants.

The proteins, or nitrogen-rich foods, include all animal products except for fats, fish, shellfish, eggs, milk and its derivatives, certain vegetables, especially lentils, peas, and beans, as well as gelatin. Fats consist of various fats and oils that are typically consumed. Carbohydrates are made up of starchy foods, such as cereals, sugars, fruits, and most vegetables, essentially all except lentils. Different beverages and condiments offer little nutritional value but help to stimulate appetite and promote the secretion of digestive juices. Coffee, tea, and alcohol are considered stimulants.

The different classes of foods have different functions in the nourishment of the body. The proteins are primarily tissue-builders and also help somewhat in force production. The fats are essentially heat-producers, though they too help in force production. The carbohydrates are chiefly important as force-producers, though they also produce heat and to a certain extent save protein oxidation. Fat [Pg 148] is formed by all three but only in small amount by proteins. So no one food can form the whole diet but there must be variety. Carbohydrates and fats are not sufficient for life, some protein is necessary. Carbohydrates are more digestible than fats but have less potential energy. Gelatine saves waste of nitrogen, though it does not increase the supply. Water and salts are not nutritive but they aid the body processes, the water helping to dilute and dissolve substances for digestion.

The different types of foods serve various roles in nourishing the body. Proteins mainly build tissues and also contribute a bit to energy production. Fats are primarily sources of heat, but they also assist in energy production. Carbohydrates are mainly important for energy, although they also produce heat and help preserve protein from being used for energy. Fat [Pg 148] is made by all three types but only in small amounts from proteins. Therefore, no single type of food can provide a complete diet; variety is essential. Carbohydrates and fats alone aren't enough for life; some protein is necessary. Carbohydrates digest better than fats but provide less potential energy. Gelatin helps minimize nitrogen waste, although it doesn't boost the supply. Water and salts aren't nutrients, but they support the body's processes, with water helping to dilute and dissolve substances for digestion.

The end-product of the consumption of protein is urea, which is eliminated by the kidneys. Just where it is formed is unknown, but many think in the liver. A trifling amount of urea is also eliminated in the sweat and in the breath as well as in the feces. Proteins increase nitrogenous metabolism and also the metabolism of other foods, but the amount of nitrogen eliminated is just equal to that taken in. Probably some comes from the tissues themselves and not from the food. The oxidation of carbohydrates and fats is measured by the amount of carbon excreted. At first as much is given off as is taken in, but after a while the carbohydrate is stored up as glycogen in the liver and the fats are stored as fat.

The final product of protein consumption is urea, which is removed by the kidneys. Its exact place of formation is unclear, but many believe it's in the liver. A small amount of urea is also eliminated through sweat, breath, and feces. Proteins boost nitrogen metabolism and also the metabolism of other foods, but the nitrogen excreted matches the amount consumed. Some of it likely comes from the tissues themselves rather than the diet. The breakdown of carbohydrates and fats is indicated by the amount of carbon expelled. Initially, the amount released equals what is consumed, but over time, carbohydrates are stored as glycogen in the liver, and fats are stored as fat.

The amount of food needed varies with the person’s size and occupation, less being needed for a child than for an adult and more for a hard-working man than for one who is doing less work. In general, 100 to 130 grams of protein, 40 to 80 grams of fat, 450 to 550 grams of carbohydrates, 30 grams of salts, and 28,000 grams of water is a fair amount.

The amount of food required changes based on a person's size and job, with children needing less than adults and someone with a physically demanding job needing more than someone who's less active. Generally, a good amount includes 100 to 130 grams of protein, 40 to 80 grams of fat, 450 to 550 grams of carbohydrates, 30 grams of salt, and 28,000 grams of water.

Foods are cooked to make them more digestible and to develop their flavor, so that they will taste better. Cooking also kills germs and parasites that might be harmful. Meats should be cooked rapidly on the outside to coagulate the surface albumen and keep in the juices. The heat, besides coagulating the albumen, turns the tough parts to gelatine. In cereals the tough envelope of cellulose is broken up and in vegetables the tough fibrous parts are softened and made more digestible. [Pg 149]

Foods are cooked to make them easier to digest and to enhance their flavor, so they taste better. Cooking also eliminates germs and parasites that could be harmful. Meats should be cooked quickly on the outside to seal in the juices. The heat not only seals the juices but also transforms tough parts into gelatin. In grains, the tough outer layer of cellulose is broken down, and in vegetables, the fibrous parts are softened and made easier to digest. [Pg 149]

The Liver.—Below the diaphragm on the right and extending across above the stomach, resting in a way upon the transverse colon and the small intestine, is the liver, the largest gland in the body. It is dark reddish-brown in color and is larger in proportion in the child than in the adult. The upper surface is convex and lies in contact with the diaphragm, while the lower surface is concave to fit over the organs beneath. With a full breath it comes downward and forward, with the edge against the abdominal wall, and can be easily felt. Numerous strong ligaments, including the suspensory ligament from the diaphragm, hold it in place, and it is more firmly fixed than any other of the abdominal organs, probably on account of its large size. It is divided by fissures into five lobes, of which the most important are the right and left, the right one being the largest and containing the gall-bladder in one of its fissures.

The Liver.—Located below the diaphragm on the right and extending across above the stomach, resting somewhat on the transverse colon and the small intestine, is the liver, the largest gland in the body. It has a dark reddish-brown color and is proportionally larger in children than in adults. The upper surface is rounded and in contact with the diaphragm, while the lower surface is indented to fit over the organs below it. When you take a full breath, it moves downward and forward, with its edge pressing against the abdominal wall, making it easy to feel. Strong ligaments, including the suspensory ligament from the diaphragm, keep it in place, and it's anchored more securely than any other abdominal organs, likely due to its large size. It's divided by fissures into five lobes, with the right and left lobes being the most significant; the right lobe is the largest and houses the gall-bladder in one of its fissures.

Fig. 56.—The liver, seen from below. 1, Inferior vena cava; 2, gall-bladder. (Morrow.)

Fig. 56.—The liver, seen from underneath. 1, Inferior vena cava; 2, gall-bladder. (Morrow.)

[Pg 150] The liver tissue contains a large number of cells collected into lobules, in the center of each of which is a blood-vessel, the intralobular vein, from which a network of capillaries extends to the edge of the lobule, there being a capillary on either side of each row of cells. Between the cells also are the intercellular biliary passages, roots of the bile ducts which exist in the connective tissue between the lobules and which join to form two main ducts, one from the right and the other from the left lobe. By the union of these two ducts the hepatic duct is formed, which, after a course of one or two inches, joins the cystic duct from the gall-bladder to form the ductus communis or common bile duct.

[Pg 150] The liver tissue is made up of numerous cells grouped into lobules. In the center of each lobule is a blood vessel called the intralobular vein, which branches out into a network of capillaries that reach the edge of the lobule, with a capillary on each side of every row of cells. Between the cells, there are also intercellular biliary passages, which are the beginnings of the bile ducts found in the connective tissue between the lobules. These ducts combine to form two main ducts, one from the right lobe and the other from the left lobe. The merging of these two ducts creates the hepatic duct, which, after traveling one or two inches, joins with the cystic duct from the gallbladder to form the ductus communis or common bile duct.

The liver has a double blood supply, the hepatic artery from the celiac axis bringing nourishment to the connective tissue and the walls of the blood-vessels, while the capillaries between the cells come from the portal vein, which, being formed by the junction of the superior and inferior mesenteric, the splenic and the gastric veins, contains the proteins and carbohydrates absorbed during digestion. After its passage through the liver this blood from the portal vein is collected once more into the hepatic veins, which convey it to the inferior vena cava. During its passage, however, various changes take place, for the liver plays an important part in the metabolic processes of the body.

The liver has a double blood supply: the hepatic artery from the celiac axis delivers nutrients to the connective tissue and the walls of the blood vessels, while the capillaries between the cells come from the portal vein. This vein is formed by the merging of the superior and inferior mesenteric veins, the splenic vein, and the gastric veins, and it carries the proteins and carbohydrates absorbed during digestion. After passing through the liver, this blood from the portal vein is collected again into the hepatic veins, which transport it to the inferior vena cava. During this journey, however, various changes occur, as the liver plays a crucial role in the body's metabolic processes.

The liver has two principal functions, the secreting of bile and the storing up of glycogen. The secretion of bile, which is a very important aid to digestion, is probably a reflex act, the presence of peptones in the portal blood after meals acting as a stimulant to the liver cells. For food at once increases the secretion of bile, which is poured from the cells into the small bile ducts and finally passes into the hepatic duct and so to the gall-bladder, where it is stored until needed. Although the flow from the liver is constant, the amount secreted reaches its maximum when the food gets down into the small intestine, that is, four or five hours after eating, there being a lull [Pg 151] before that. Apart from the process of secretion, the manufacture of the bile pigments, bilirubin and biliverdin, which are made from the hemoglobin of the blood, seems to require some special action on the part of the liver cells.

The liver has two main functions: producing bile and storing glycogen. The production of bile, which is essential for digestion, is likely a reflex action triggered by the presence of peptones in the portal blood after meals. Eating increases bile production, which flows from the liver cells into the small bile ducts and then into the hepatic duct, where it’s stored in the gallbladder until needed. Although the liver continuously produces bile, the amount released peaks when food reaches the small intestine, about four or five hours after eating, with a pause [Pg 151] beforehand. Besides secretion, the production of bile pigments, bilirubin and biliverdin, derived from the blood’s hemoglobin, seems to require specific activity from the liver cells.

The glycogen, which is manufactured and stored in the liver cells, is a clear hyaline substance, akin to starch and capable of being converted into sugar by the starch ferment. Probably there is some such ferment in the blood which converts the glycogen into sugar as soon as it passes from the liver into the blood, though what it is, is not known. Neither is it known just how glycogen is formed, but it is manufactured chiefly after a mixed meal in which carbohydrates predominate, proteins having little and fats no effect upon its formation. It is undoubtedly formed from the sugar in the portal blood and the process requires some work on the part of the liver cell itself. Probably there is always some sugar in the circulating blood which, as it is used up, must be made good. If there it not enough in the diet, the liver supplies the deficiency from its store of glycogen.

The glycogen, produced and stored in liver cells, is a clear, glassy substance similar to starch and can be converted into sugar by starch enzymes. There’s likely some enzyme in the blood that turns glycogen into sugar as soon as it moves from the liver into the bloodstream, although its identity isn’t known. It’s also unclear how exactly glycogen is created, but it mainly occurs after a mixed meal where carbohydrates are the main component—proteins have a minor effect, and fats have none on its production. It's definitely made from the sugar in the portal blood, and the process requires action from the liver cells. There is probably always some sugar in the circulating blood that needs to be replenished as it gets used up. If there isn’t enough sugar in the diet, the liver compensates for the shortfall by using its glycogen reserves.

Glycogen is found also in the muscles, in the placenta as food for the fetus, in leucocytes, and to a slight extent in cartilage. In fact, it is the form in which carbohydrate material is supplied to the tissues as needed. Normally, much of the sugar is used up by the blood and its cells in metabolism, giving rise to heat and energy. In muscles glycogen is probably digested as lactic acid, as before action muscle is neutral or slightly alkaline and after action acid.

Glycogen is also found in the muscles, in the placenta as nourishment for the fetus, in white blood cells, and to a small extent in cartilage. Essentially, it’s the way carbohydrates are delivered to the tissues when needed. Typically, much of the sugar is utilized by the blood and its cells during metabolism, generating heat and energy. In muscles, glycogen is likely broken down into lactic acid, as muscles are neutral or slightly alkaline before activity and turn acidic afterward.

When the liver is deranged and allows the glycogen to pass out into the blood too freely, or when the glycogen is not held as such but turned to sugar and passed out in large quantities, sugar in the urine or diabetes mellitus results.

When the liver is malfunctioning and lets glycogen leak into the blood too easily, or when glycogen is not stored properly but converted into sugar and released in large amounts, sugar in the urine or diabetes mellitus occurs.

Besides its secreting function the liver has an eliminative function and plays an important part in purifying the blood, removing from it many poisonous and narcotic substances. It is thought by some, though [Pg 152] it has not been proved, that urea, the end-product of protein metabolism, which is brought by the blood to the kidneys and there excreted, is formed in the liver. At any rate, urea is formed not only from the nitrogenous food eaten but from the metabolism of protein substances in the tissues, being purely a waste product, from which the nutritious substances have been absorbed. The amount thrown off is an accurate gauge of the amount of protein metabolism going on. The process of its manufacture is doubtless very complex.

Besides its role in secretion, the liver also has an eliminative function and is crucial for purifying the blood by removing various toxic and narcotic substances. Some believe, although it hasn't been proven, that urea, the final product of protein metabolism, is produced in the liver and then carried by the blood to the kidneys for excretion. In any case, urea is generated not only from the nitrogen-rich food consumed but also from protein metabolism in the tissues, serving as a waste product after the nutritious substances have been absorbed. The amount excreted is a reliable indicator of the level of protein metabolism occurring. The process of its production is undoubtedly quite complex.

Ptosis or dropping of the liver sometimes occurs and is due to the stretching of the ligaments. Rupture is common, generally as the result of a fall from a height, on account of its size and friability. The liver is also subject to many diseases. Cirrhosis occurs in people who drink a good deal and in its later stages is accompanied by ascites, an accumulation of fluid in the abdominal cavity. When there is a general accumulation of fluid throughout the body it is known as anasarca. Syphilis causes enlargement of the liver. Abscesses occur, perhaps oftener in the tropics than farther north, and may break into the lungs, stomach, or intestine.

Ptosis or dropping of the liver can happen due to stretching of the ligaments. Rupture is common, usually from a fall from a height, because of its size and fragility. The liver is also vulnerable to many diseases. Cirrhosis develops in people who drink heavily and, in the later stages, is accompanied by ascites, which is a buildup of fluid in the abdominal cavity. When there’s a general buildup of fluid throughout the body, it’s referred to as anasarca. Syphilis can cause the liver to enlarge. Abscesses occur, perhaps more often in tropical regions than in northern areas, and may rupture into the lungs, stomach, or intestine.

The Gall-bladder.—The gall-bladder, which is simply a reservoir for the bile, is a pear-shaped organ three inches long and one inch broad. It lies in a fossa on the under side of the liver, with the large end or fundus touching the abdominal wall just below the ninth costal cartilage. Here it can be felt as a small mass in empyema of the gall-bladder. Normally it holds a little over one ounce, but with occlusion it may become stretched. Its duct is the cystic duct, which joins the hepatic duct in the common bile duct, but bile only passes up into the gall-bladder when the opening into the duodenum is closed, that is, between meals.

The Gall-bladder.—The gall-bladder, which is simply a storage space for bile, is a pear-shaped organ about three inches long and one inch wide. It sits in a fossa on the under side of the liver, with the larger end, or fundus, touching the abdominal wall just below the ninth rib cartilage. Here it can be felt as a small mass in cases of gall-bladder inflammation. Normally, it holds just over one ounce, but it can stretch if it becomes blocked. Its duct is the cystic duct, which connects with the hepatic duct to form the common bile duct, but bile only flows into the gall-bladder when the opening into the duodenum is closed, meaning between meals.

If one of the bile ducts is stopped up by a stone or cancer or for any other cause, the bile backs up in the liver, the pigments are absorbed [Pg 153] into the circulation, and jaundice results. In this condition operation is dangerous, as the time of coagulation of the blood, normally five minutes or less, is much delayed. Gall stones, formed largely of bile pigments and cholesterin, sometimes collect in the gall-bladder, where they cause irritation and may give rise to empyema of the gall-bladder. The stones vary in size from a pea to a hen’s egg and when small may be very numerous.

If one of the bile ducts is blocked by a stone, cancer, or another reason, bile backs up in the liver, pigments are absorbed [Pg 153] into the bloodstream, and jaundice occurs. In this situation, surgery is risky because the time it takes for blood to clot, typically five minutes or less, is significantly extended. Gallstones, mainly made up of bile pigments and cholesterol, can sometimes accumulate in the gallbladder, causing irritation and potentially leading to empyema of the gallbladder. The stones can range in size from a pea to a hen’s egg, and when they are small, they can be quite numerous.

Fig. 57.—The pancreas, spleen, gall-bladder, etc., showing their relations.
(After Sobotta.)

Fig. 57.—The pancreas, spleen, gallbladder, etc., showing how they are connected.
(After Sobotta.)

The Pancreas.—Another accessory organ of digestion is the pancreas, the abdominal salivary gland, as it is sometimes called on account of its close resemblance to the parotid gland. This is a grayish-white racemose gland, six and a half inches long by one and a half inches wide and one inch thick, lying behind the stomach on a level with the first and second lumbar vertebræ and shaped like a pistol with its handle toward the right. In an emaciated person it can [Pg 154] be felt. The pancreatic duct runs the whole length of the gland from left to right and conveys the pancreatic juice from various little glands in the substance of the organ to the duodenum, into which it empties along with the common bile duct by a common orifice. The arteries are from the celiac axis and superior mesenteric, the veins belong to the portal system, and the nerves come from the solar plexus.

The Pancreas.—Another accessory organ of digestion is the pancreas, the abdominal salivary gland, as it’s sometimes called due to its close resemblance to the parotid gland. This is a grayish-white racemose gland, about six and a half inches long, one and a half inches wide, and one inch thick, located behind the stomach at the level of the first and second lumbar vertebrae, shaped like a pistol with the handle pointing to the right. In a very thin person, it can be felt. The pancreatic duct runs the entire length of the gland from left to right and carries the pancreatic juice from several small glands within the organ to the duodenum, where it empties along with the common bile duct at a shared opening. The arteries come from the celiac axis and superior mesenteric, the veins are part of the portal system, and the nerves originate from the solar plexus.

Surgically the pancreas is of no special importance, though acute pancreatitis does occasionally occur and is a very serious condition and one hard to diagnose.

Surgically, the pancreas isn't of particular significance, although acute pancreatitis can sometimes happen, and it's a very serious condition that's difficult to diagnose.

The Spleen.—The largest and most important of the ductless glands is the spleen, an oblong, flattened organ lying deep in the left hypochondriac region between the stomach and diaphragm above the descending colon, and corresponding to the ninth, tenth, and eleventh ribs. It is soft, brittle, and very vascular. Its artery is a branch of the celiac axis and the vein belongs to the portal system. Its nerves are the pneumogastric and branches from the solar plexus. The function is not well understood but probably it is connected with or related to the vascular system in some way. Perhaps it manufactures blood corpuscles.

The Spleen.—The largest and most important of the ductless glands is the spleen, an elongated, flattened organ located deep in the left hypochondriac region between the stomach and diaphragm, above the descending colon, and corresponding to the ninth, tenth, and eleventh ribs. It is soft, fragile, and highly vascular. Its artery is a branch of the celiac axis, and the vein is part of the portal system. Its nerves come from the pneumogastric and branches of the solar plexus. The function is not well understood, but it is likely connected to the vascular system in some way. It may even produce blood cells.

The spleen varies more in size than any other organ. Normally it cannot be felt, but in typhoid it usually can. It is generally atrophied in old age and hypertrophied in almost all acute infectious diseases, especially in typhoid fever and malaria. In leukemia it is often greatly enlarged. Sometimes in violent falls it is ruptured and there is considerable hemorrhage.

The spleen changes size more than any other organ. Normally, it can’t be felt, but in typhoid, it usually can be. It tends to shrink in old age and swell in almost all acute infectious diseases, especially in typhoid fever and malaria. In leukemia, it’s often significantly enlarged. Sometimes, in intense falls, it can be ruptured, leading to considerable bleeding.

The Suprarenal Capsules.—The other ductless glands, the suprarenal capsules, yellowish triangular bodies, are situated just above and in front of the kidneys. Their function is important but not well understood. Death, accompanied by great muscular weakness, follows the removal of both, and when they are diseased, similar weakness is observed and the skin becomes bronzed. Injection of the extract of the [Pg 155] suprarenals stimulates the muscular system. So probably they secrete into the blood minute quantities of a substance or substances beneficial to the body, especially to the muscular system.

The Suprarenal Capsules.—The other ductless glands, the suprarenal capsules, are yellowish triangular structures located just above and in front of the kidneys. Their function is important but not fully understood. When both are removed, death usually follows due to severe muscle weakness, and similar weakness occurs when they are diseased, with the skin taking on a bronze appearance. Injecting an extract from the [Pg 155] suprarenals stimulates the muscular system. So, they likely release small amounts of substances into the blood that are beneficial to the body, especially for the muscular system.

Fig. 58.—Diagram of the relation of kidney to viscera, spine, and surface points.
(American Text-Book of Surgery.)

Fig. 58.—Diagram showing the relationship of the kidney to the organs, spine, and surface points.
(American Text-Book of Surgery.)

The Kidneys.—The two kidneys lie on either side of the vertebræ at the back of the abdominal cavity and behind the peritoneum, between the last dorsal and the third lumbar vertebræ, their inner edge being about one inch from the spinous processes. They are bean-shaped, four inches long, two inches wide, and one inch thick, and are embedded in a mass of fat and loose areolar tissue. They can be felt only when misplaced or when enlarged, as by tuberculosis or malignant disease.

The Kidneys.—The two kidneys are located on either side of the spine at the back of the abdominal cavity and behind the peritoneum, between the last thoracic and the third lumbar vertebrae, with their inner edge being about one inch from the spinous processes. They are bean-shaped, four inches long, two inches wide, and one inch thick, and are surrounded by a layer of fat and loose connective tissue. They can only be felt when they are displaced or enlarged, such as in cases of tuberculosis or cancer.

The whole kidney is enveloped in a fibrous capsule which normally may be peeled off but which in some diseases becomes adherent. On the internal border is a fissure or hilum, through which pass the blood-vessels and the ureter. Upon entering, the ureter dilates into a sac, the pelvis of the kidney, into which project the Malpighian pyramids of the medullary substance, a substance made up of the [Pg 156] straight uriniferous tubules and blood-vessels. Outside the medullary substance and just under the capsule is the cortex, containing the Malpighian bodies, blood-vessels, and the convoluted tubules or loops of Henle. Each Malpighian body contains within a capsule a plexus of capillaries, the glomerulus, with an afferent arteriole and an efferent vein. The renal artery is a branch of the aorta and the nerves are from the solar plexus.

The whole kidney is surrounded by a fibrous capsule that can usually be peeled away, but in some diseases, it sticks. On the inside edge is a fissure or hilum, through which the blood vessels and the ureter pass. When the ureter enters, it expands into a sac, the pelvis of the kidney, into which the Malpighian pyramids of the medullary substance extend; this substance is made up of the [Pg 156] straight uriniferous tubules and blood vessels. Outside the medullary substance and just beneath the capsule is the cortex, which contains the Malpighian bodies, blood vessels, and the convoluted tubules or loops of Henle. Each Malpighian body consists of a capsule containing a network of capillaries, the glomerulus, along with an afferent arteriole and an efferent vein. The renal artery branches off from the aorta, and the nerves come from the solar plexus.

Fig. 59.—A longitudinal section
of the kidney. (Leroy.)
a, Renal artery; c, cortex;
m, medulla; u, ureter.

Fig. 59.—A side view
of the kidney. (Leroy.)
a, Renal artery; c, cortex;
m, medulla; u, ureter.

Fig. 60.—A Malpighian body
or corpuscle. (Leidy.)
a, Afferent artery;
e, efferent vessel;
c, capillaries;
k, commencement of
uriniferous tubule;
h, uriniferous tubule.

Fig. 60.—A Malpighian body
or corpuscle. (Leidy.)
a, Afferent artery;
e, efferent vessel;
c, capillaries;
k, start of
uriniferous tubule;
h, uriniferous tubule.

The Urine.—As the blood passes through the glomeruli, the urine is filtered off as it were, probably by a process of transudation rather than simple filtration. The cells lining the tubules also play an important part in its formation, not by secreting new substances but by taking up those brought by the blood and discharging them into the convoluted tubules, from which the urine passes through the straight tubules of the medulla to the pelvis, to be carried thence by the [Pg 157] ureter. The process of the formation of the urine, therefore, is not purely a process of secretion but requires some action on the part of the kidney, though no new substances are secreted in the kidney.

The Urine.—As blood flows through the glomeruli, urine is filtered out, likely through a process of transudation rather than simple filtration. The cells lining the tubules are also crucial in its formation, not by producing new substances but by absorbing those from the blood and releasing them into the convoluted tubules, from which urine then flows through the straight tubules of the medulla to the pelvis, to be carried onward by the [Pg 157] ureter. Therefore, the process of urine formation is not just a secretion process but also involves some action from the kidneys, although no new substances are created in the kidneys.

The passage of the urine down through the ureters is assisted by a kind of peristaltic action in the walls of the ureters and it is expelled from the body by the act of micturition, which is mostly voluntary, though a certain amount of nervous mechanism controls it. The seat of this nervous mechanism is in the lumbar enlargement of the spinal cord. In some nervous conditions, especially where there is injury to the spinal cord, there is involuntary micturition.

The flow of urine down through the ureters is helped by a wave-like motion in the walls of the ureters, and it is released from the body through the act of urination, which is mostly under our control, although some nervous system regulation plays a role. This regulation originates from the lumbar enlargement of the spinal cord. In certain nervous conditions, particularly in cases of spinal cord injury, there can be uncontrolled urination.

The urine is a watery solution containing many waste products, especially urea. It is generally amber in color, varying in shade with circumstances, with an aromatic, characteristic odor when fresh. It is acid in reaction and has a specific gravity of about 1020, though this too varies with circumstances. Besides water, which is its chief constituent, it contains urea, uric acid, organic acids, urates, inorganic salts, including sodium chloride and phosphates of calcium and magnesium, a certain amount of ammonia, and certain pigments. Its acidity is due to acid sodium phosphate in solution but varies with the food, and in disease the urine may become alkaline when passed. After standing a few hours in a warm place it decomposes and becomes alkaline.

The urine is a watery solution that contains various waste products, primarily urea. It's usually amber in color, with shades that change depending on different factors, and has a distinct, characteristic smell when fresh. It’s acidic and has a specific gravity of about 1.020, although this can fluctuate based on conditions. Besides water, which is its main component, it includes urea, uric acid, organic acids, urates, and inorganic salts such as sodium chloride and phosphates of calcium and magnesium, along with some ammonia and certain pigments. Its acidity comes from dissolved acid sodium phosphate but can vary with diet, and in some illnesses, urine may become alkaline when excreted. If it sits in a warm place for a few hours, it starts to decompose and turns alkaline.

The quantity, which is normally three pints or fifteen hundred cubic centimeters in twenty-four hours, varies with the amount of fluid drunk, the amount of perspiration, etc. The amount secreted depends chiefly, however, upon the flow of the blood through the kidneys; the greater the flow of blood, the larger the amount of urine formed; and the blood flow is determined by blood pressure and by vasomotor action. Secretion also seems to be increased by the presence of urea, which apparently serves as a stimulant to the kidney cells. [Pg 158]

The amount, which is usually three pints or fifteen hundred cubic centimeters in a day, changes based on how much fluid you drink, how much you sweat, and other factors. However, the amount produced mainly depends on the blood flow through the kidneys; the more blood that flows, the more urine is generated. This blood flow is influenced by blood pressure and vasomotor activity. It also seems that the presence of urea increases secretion, acting as a stimulant for the kidney cells. [Pg 158]

The excretion of waste materials takes place by three main channels, the lungs, skin, and kidneys, and the materials are of four kinds, urea, carbon dioxide, salts, and water. The lungs carry off carbon dioxide and water chiefly, the skin these and inorganic salts, while the kidneys eliminate practically all the urea as well as inorganic salts and water. When the kidneys are not working the skin carries off much urea. In fact, a close relationship exists between the kidneys and the skin in the matter of excretion. Thus, with increased perspiration in warm weather comes decreased urine, while in cold weather the blood is sent in and the urine increased in amount.

The body gets rid of waste materials through three main channels: the lungs, skin, and kidneys. There are four types of waste: urea, carbon dioxide, salts, and water. The lungs primarily remove carbon dioxide and water, the skin handles those along with inorganic salts, and the kidneys eliminate most of the urea as well as inorganic salts and water. When the kidneys aren't functioning properly, the skin can excrete a significant amount of urea. In fact, there's a close relationship between the kidneys and the skin when it comes to waste removal. In hot weather, increased sweating leads to less urine production, while in cold weather, blood flow increases to the kidneys, resulting in more urine being produced.

To incite action of the kidneys drugs known as diuretics may be used. These act in two ways, by stimulating the kidney cells directly and by acting on the general circulation or nervous system. Any emotional or nervous excitement increases the flow of urine.

To stimulate kidney function, drugs called diuretics may be used. They work in two ways: by directly stimulating kidney cells and by influencing the overall circulation or nervous system. Any emotional or nervous excitement boosts urine flow.

There are certain abnormal constituents of urine, of which the two most important are albumen and sugar. The former is found only when there is some disturbance of the kidneys, ureters, or bladder, and its presence usually denotes some change in the cells lining the urinary tract. It may occur in congestion of the kidney as well as in disease. Sugar is found only in diabetes, the amount varying with the severity of the disease. In jaundice certain bile pigments are present in the urine, giving it a dark brown color and to the foam a greenish-yellow color. Even normal urine has some sediment upon standing, consisting of cells from the urinary tract and mucus. In very acid urine after standing a heavy sediment, whitish or pinkish, i.e., brick dust, in color, is thrown down. It does not necessarily denote disease, but shows the urine is acid and concentrated. In alkaline urine there is a sediment due to phosphates.

There are certain unusual components in urine, with the two most important being albumin and sugar. The first is only present when there’s some issue with the kidneys, ureters, or bladder, and its presence usually indicates a change in the cells lining the urinary tract. It can occur during kidney congestion as well as in various diseases. Sugar is found only in diabetes, and the amount varies based on the severity of the condition. In jaundice, certain bile pigments can be found in the urine, which gives it a dark brown color and the foam a greenish-yellow tint. Even normal urine has some sediment after sitting, composed of cells from the urinary tract and mucus. In very acidic urine, after sitting, a heavy sediment that is whitish or pinkish in color, known as brick dust, can settle. This doesn’t necessarily indicate disease but shows the urine is acidic and concentrated. In alkaline urine, sediment occurs due to phosphates.

Rupture of the kidney occurs but is not so serious as rupture of the [Pg 159] liver or spleen because the kidney is situated outside of the peritoneum. It necessitates the removal of the kidney, however, and when for any reason one kidney is removed the other increases in size and does double work to compensate for the loss. Removal of both kidneys means death. Sometimes the kidney becomes loose and moves about, a condition known as floating kidney. Perinephritic abscess is abscess in the loose fatty tissue about the kidney.

Rupture of the kidney can happen but is not as serious as a rupture of the [Pg 159] liver or spleen because the kidney is located outside of the peritoneum. It does require the removal of the kidney, though, and when one kidney is taken out, the other grows larger and works harder to make up for the loss. Removing both kidneys leads to death. Sometimes the kidney can become loose and move around, a condition referred to as floating kidney. Perinephritic abscess is an abscess in the loose fatty tissue surrounding the kidney.

Fig. 61.—The urinary organs
viewed from behind.

Fig. 61.—The urinary organs
seen from the back.

The Ureters, one for each kidney, are tubes the size of a goose quill and about fourteen inches long, extending from the hilum of the kidney to the base of the bladder. They have three coats, an internal mucous, a muscular, and an external fibrous coat, this last being continuous with the cortex of the kidney and the fibrous tissue of the bladder. In the female the ureters may be felt through the wall of the vagina as they come into the bladder. In tubercular disease of one kidney the ureter becomes inflamed and enlarged and through the vagina feels almost like a lead pencil, a sure diagnostic sign.

The Ureters, one for each kidney, are tubes about the size of a goose quill and roughly fourteen inches long, running from the kidney's hilum to the base of the bladder. They consist of three layers: an inner mucous layer, a muscular layer, and an outer fibrous layer, the last of which is continuous with the kidney's cortex and the fibrous tissue of the bladder. In females, the ureters can be felt through the vaginal wall as they enter the bladder. In cases of tuberculosis affecting one kidney, the ureter becomes inflamed and swollen, and can be felt through the vagina like a lead pencil, which is a clear diagnostic indicator.

The Bladder and Urethra.—In their course to the bladder [Pg 160] the ureters pass from the abdominal into the pelvic cavity, but before describing the pelvis itself it will be well to complete the account of the urinary organs by considering the bladder and urethra. The bladder is the reservoir for the urine and has muscular walls lined with mucous membrane. A peritoneal coat covers the upper surface and is reflected to the walls of the abdomen and pelvis. It is situated back of the os pubis, the front bone of the pelvis, with its base or fundus directed downward and backward. Normally it is in the pelvis, but when much distended it mounds up into the abdominal cavity, where it can be felt in front as a tumor. It rests on the rectum in the male and on the cervix in the female and is held in place by numerous ligaments. When empty it may be Y-shaped, but it becomes oval when distended. Its capacity is about one pint.

The Bladder and Urethra.—As the ureters move from the abdominal cavity into the pelvic cavity, it's important to finish discussing the urinary organs by looking at the bladder and urethra. The bladder acts as a storage space for urine and has muscular walls lined with a mucous membrane. The upper surface is covered by a peritoneal layer that extends to the walls of the abdomen and pelvis. It is located behind the pubic bone, the front bone of the pelvis, with its base or fundus directed downward and backward. Normally, it sits in the pelvis, but when it’s very full, it can push into the abdominal cavity, where it may be felt as a swelling. In males, it rests on the rectum, while in females, it sits on the cervix, and it is held in place by various ligaments. When empty, it may take on a Y-shape, but it becomes oval when full. Its capacity is about one pint.

The lower abdominal wall and the anterior wall of the bladder may be wanting congenitally. In paralysis of the sphincter at the neck of the bladder distention results. Stones may be found in the bladder.

The lower abdominal wall and the front wall of the bladder may be underdeveloped from birth. If the sphincter at the bladder neck is paralyzed, it can lead to swelling. Stones may be present in the bladder.

From the neck of the bladder the urine passes out of the body through the urethra. This in the male passes down through the penis and is about ten inches long. Except when urine is passing it is a transverse slit with the upper and under surfaces in contact, while at the end of the penis the slit of the meatus urinarius is vertical. When the penis is flaccid, the urethra describes a sharp curve before its entrance into the bladder, but it becomes approximately straight when the penis is raised at right angles to the body—an important point to remember in catheterization.

From the neck of the bladder, urine exits the body through the urethra. In males, it travels through the penis and is about ten inches long. When urine isn’t flowing, it appears as a horizontal slit with the upper and lower surfaces touching, while at the tip of the penis, the opening of the urethra is vertical. When the penis is relaxed, the urethra takes a sharp curve before entering the bladder, but it becomes fairly straight when the penis is raised at a right angle to the body—an important detail to keep in mind during catheterization.

In the female the urethra is straight and much shorter, being only about one and a half inches long. The meatus urinarius is in the anterior vaginal wall about one inch behind the clitoris.

In females, the urethra is straight and much shorter, measuring only about one and a half inches long. The meatus urinarius is located in the front wall of the vagina, about one inch behind the clitoris.

Sometimes the urethra is ruptured in a fall. Stricture of the urethra occurs sometimes after gonorrhoea, owing to the formation of scar tissue following ulcer.

Sometimes the urethra is ruptured in a fall. Stricture of the urethra can sometimes happen after gonorrhea due to scar tissue forming after an ulcer.


CHAPTER XI.
THE PELVIS AND THE GENITALS.

The Pelvis.—Before taking up the pelvic organs, the pelvis itself should be described. The name pelvis has been given to the bony ring which is interposed between the spine and the femurs on account of its resemblance to a basin. At the back of this basin or pelvis are the sacrum and coccyx, already described in connection with the back, and at the sides and meeting in the median line in front are the two ossa innominata or nameless bones, so called on account of their peculiar and indescribable shape. At birth each os innominatum is made up of three bones, the ilium, ischium, and pubes, but about [Pg 162] the age of puberty the three become welded into one. At their point of junction is the cavity of the acetabulum for articulation with the head of the femur or thigh bone.

The Pelvis.—Before discussing the pelvic organs, the pelvis itself needs to be described. The term pelvis refers to the bony ring that sits between the spine and the femurs, resembling a basin. At the back of this basin or pelvis are the sacrum and coccyx, which have already been described in relation to the back. On the sides and meeting in the middle at the front are the two ossa innominata or nameless bones, named for their unique and hard-to-describe shape. At birth, each os innominatum consists of three bones: the ilium, ischium, and pubes, but around the time of puberty, these three bones fuse into one. At their point of junction is the acetabulum cavity, which allows for articulation with the head of the femur or thigh bone.

Fig. 62.—Front view of the pelvis, with its ligaments. (Dorland.) a, Anterior sacro-iliac ligament; b, iliofemoral ligament; c, obturator membrane; d, symphysis pubis; e, sacro-sciatic ligament.

Fig. 62.—Front view of the pelvis, showing its ligaments. (Dorland.) a, Anterior sacro-iliac ligament; b, iliofemoral ligament; c, obturator membrane; d, symphysis pubis; e, sacro-sciatic ligament.

Fig. 63.—The right innominate bone.
(After Toldt.)

Fig. 63.—The right innominate bone.
(After Toldt.)

The upper, expanded portion of the os innominatum is the ilium, whose upper border is known as the crest and which has two spinous processes front and back, a superior and an inferior, the superior spine being in each case the larger. These spines, especially the anterior superior spines, and the crest give attachment to many muscles, and to the outer surface of the bone the gluteal muscles are attached. The anterior superior spine is also important in making measurements to ascertain whether both legs are of equal length. [Pg 163]

The upper, expanded part of the os innominatum is the ilium, with its top edge called the crest. It features two spinous processes at the front and back, a superior and an inferior, with the superior spine being larger in each case. These spines, especially the anterior superior spines, along with the crest, serve as attachment points for many muscles, while the gluteal muscles are connected to the outer surface of the bone. The anterior superior spine is also crucial for measuring and determining if both legs are the same length. [Pg 163]

Below the ilium posteriorly is the body of the ischium, which has on its lower edge a tuberosity, the prominent bone on which one sits. Near the upper edge is the spine of the ischium, between which and the posterior inferior spine of the ilium is the greater sacro-sciatic notch for the passage of vessels and nerves, including the sciatic nerves. From the tuberosity the ramus extends forward below the obturator foramen, a large opening between the ischium and the pubes, also for the passage of vessels and nerves, to meet the pubes, the last and smallest of the three bones which go to make up the os innominatum.

Below the ilium at the back is the body of the ischium, which has a tuberosity along its lower edge, the hard bump where one sits. Near the upper edge is the spine of the ischium, and between it and the posterior inferior spine of the ilium is the greater sacro-sciatic notch that allows the passage of blood vessels and nerves, including the sciatic nerves. From the tuberosity, the ramus extends forward below the obturator foramen, a large hole between the ischium and the pubes, also for the passage of blood vessels and nerves, meeting the pubes, which is the last and smallest of the three bones that make up the os innominatum.

The anterior surface of each pubes presents a crest, ending externally in a spine, and the two pubic bones join in front in the symphysis pubis. The bone gets its name from the growth of pubic hairs over this region at puberty.

The front surface of each pubes has a ridge that ends in a point on the outside, and the two pubic bones connect at the front at the symphysis pubis. The bone is named for the growth of pubic hair in this area during puberty.

Fig. 64.—Diameters of the pelvis: d, antero-posterior; o b, oblique; t r, transverse. (de Nancrede.)

Fig. 64.—Pelvis dimensions: d, front to back; o b, diagonal; t r, side to side. (de Nancrede.)

Anteriorly the ossa innominata support the external organs of generation, while within are the internal organs of generation. On the inner surface of the ilium, slightly above the level of the acetabulum, is the ileo-pectineal line, above which lie the iliac fossæ. A plane drawn through the prominence of the sacrum, the ileo-pectineal lines, and the upper margin of the symphysis pubis serves to divide the upper or false pelvis from the lower or true pelvis. The false [Pg 164] pelvis, which is the larger, serves to support the intestines and to take part of the weight from the abdominal walls, while the true pelvis, being more surrounded by bone and so capable of affording more protection, guards the internal organs of generation. The lower circumference of the pelvis is known as the outlet. In the female the bones are lighter, the sacrum less curved, and the diameters greater than in the male.

Previously, the innominate bones support the external reproductive organs, while the internal reproductive organs are located within. On the inner surface of the ilium, just above the level of the acetabulum, is the ileo-pectineal line, above which are the iliac fossæ. A plane drawn through the prominence of the sacrum, the ileo-pectineal lines, and the upper edge of the pubic symphysis divides the upper or false pelvis from the lower or true pelvis. The false [Pg 164] pelvis, which is larger, supports the intestines and helps take some of the weight off the abdominal walls, while the true pelvis, being more encased in bone and thus providing greater protection, safeguards the internal reproductive organs. The lower edge of the pelvis is known as the outlet. In females, the bones are lighter, the sacrum is less curved, and the diameters are larger compared to males.

On the whole, the pelvic bones are well covered in with muscles. The anterior superior spine, however, is easily felt in front and the whole crest can be felt back to the posterior superior spine. The tuberosity of the ischium also can be felt, especially when the thigh is flexed, for it is largely uncovered of muscles. The spine of the os pubis can always be felt, on a level with the great trochanter, and the relation of its position to that of a hernia shows whether the rupture is above or below Poupart’s ligament, that is, whether it is inguinal or femoral.

Overall, the pelvic bones are covered well by muscles. However, the anterior superior spine is easy to feel in the front, and the entire crest can be felt back to the posterior superior spine. The tuberosity of the ischium can also be felt, especially when the thigh is bent, as it is mostly uncovered by muscles. The spine of the pubis can always be felt, level with the greater trochanter, and its position in relation to a hernia indicates whether the rupture is above or below Poupart’s ligament, meaning whether it is inguinal or femoral.

Occasionally there is lack of development of the pubic bones for two or three inches and the bladder is exposed. Fracture of the pelvis may occur, perhaps with injury to the viscera. The acetabulum may be fractured or the sacrum broken, with injury to the sacral plexus of nerves, causing paralysis of the lower extremities and of the sphincters, with resultant involuntary passage of urine and feces, and in childbirth the coccyx is often broken. In rickets there may be great deformity of the pelvis, causing trouble in childbirth later in life. Osteomalacia is a disease of adults, in which the bones are soft and the weight pushes the promontory of the sacrum forward and approximates the sides of the pelvis.

Sometimes, the pubic bones may not develop fully by two or three inches, leaving the bladder exposed. A pelvic fracture can happen, possibly injuring the internal organs. The acetabulum might be fractured, or the sacrum could break, damaging the sacral plexus of nerves, which can lead to paralysis in the lower limbs and the sphincters, resulting in involuntary urination and defecation. During childbirth, it's common for the coccyx to break. In rickets, there can be significant deformity of the pelvis, leading to complications in childbirth later on. Osteomalacia is a disease that affects adults, making the bones soft, which causes the weight to push the sacral promontory forward and brings the sides of the pelvis closer together.

The Male Generative Organs.—The male generative organs consist of the prostate gland, testes, and penis.

The Male Generative Organs.—The male reproductive organs include the prostate gland, testes, and penis.

The prostate gland is shaped like a small horse-chestnut and is composed of numerous glands from which come a dozen or more excretory ducts. It surrounds the neck of the bladder and the beginning of the [Pg 165] urethra and is next to the rectum, through which an examination may be made to determine its size. For it often enlarges in elderly men, the frequent passage of urine in small amounts being a symptom of enlarged prostate.

The prostate gland is shaped like a small horse chestnut and consists of many glands that lead to a dozen or more ducts. It surrounds the neck of the bladder and the start of the [Pg 165] urethra and is located next to the rectum, where a doctor can examine it to check its size. It often enlarges in older men, with frequent urination in small amounts being a common symptom of an enlarged prostate.

The procreating glands, which secrete the spermatozoa or semen, are two in number, the testes or testicles, and are homologous to the ovaries in the female. They are ovoid in form and are suspended by the spermatic cords in a sac, the scrotum, back of the penis. During early fetal life they are in the back of the abdomen near the kidneys, but before birth they descend along the inguinal canals into the scrotum. The excretory duct of the testis is called the vas deferens. It passes up by the spermatic cord through the inguinal canal into the pelvis to the base of the bladder and at the base of the prostate joins the duct of the vesicula seminalis to form the ejaculatory duct. The two vesiculæ seminales are small receptacles for the semen lying in contact with the base of the bladder and secrete a fluid with which they dilute the semen. The ejaculatory duct terminates near the prostate in the urethra by a slit-like orifice on each side, the spermatozoa being finally excreted through the urethra.

The reproductive glands, which produce sperm or semen, are two in number: the testes or testicles, and they are equivalent to the ovaries in females. They have an oval shape and are suspended by the spermatic cords in a pouch called the scrotum, located behind the penis. During early fetal development, they are positioned in the back of the abdomen near the kidneys, but before birth, they move down through the inguinal canals into the scrotum. The duct that carries sperm from the testis is called the vas deferens. It travels upward alongside the spermatic cord through the inguinal canal into the pelvis to the base of the bladder and then connects with the duct of the seminal vesicle at the base of the prostate to form the ejaculatory duct. The two seminal vesicles are small pouches for semen that are located next to the base of the bladder and produce a fluid that dilutes the semen. The ejaculatory duct ends near the prostate by opening into the urethra through a slit-like opening on each side, allowing the sperm to be expelled through the urethra.

The penis is the external organ of generation in the male and is attached to the pubes and the anterior part of the ischium. It is composed of erectile tissue and encloses the urethra, the meatus urinarius appearing at its end as a vertical slit. Toward the end the skin of the penis is loose and is prolonged forward in what is known as the prepuce or foreskin. It is this that is clipped away in circumcision.

The penis is the external reproductive organ in males and is connected to the pubic area and the front part of the ischium. It consists of erectile tissue and surrounds the urethra, with the meatus urinarius appearing at its tip as a vertical opening. Near the tip, the skin of the penis is loose and extends forward in what is called the prepuce or foreskin. This is the part that is removed during circumcision.

The Female Generative Organs.—The female generative organs include the ovaries, Fallopian tubes, uterus, vagina, and the external genitalia or vulva.

The Female Reproductive Organs.—The female reproductive organs include the ovaries, fallopian tubes, uterus, vagina, and the external genitalia or vulva.

The ovaries, which are homologous to the testes in the male, are two flattened oval bodies, grayish pink in color, suspended from the [Pg 166] lateral or broad ligaments which fasten the uterus to the walls of the pelvis. They are one and a quarter inches long, three-quarters of an inch wide, and half an inch thick and are attached at the upper end to one of the fimbriæ of the Fallopian tubes. They consist of numerous Graafian follicles embedded in a fibrous stroma, each follicle containing an ovum about ¹/₁₂₅ inch in diameter and just visible to the naked eye. When a follicle ruptures and discharges an ovum, an irregular yellow spot, the corpus luteum, appears at the point of rupture. After ordinary menstruation it is known as the false corpus luteum and after conception as the true one, this one being larger and lasting longer.

The ovaries, which are similar to the male testes, are two flattened oval shapes, grayish-pink in color, suspended from the [Pg 166] lateral or broad ligaments that attach the uterus to the walls of the pelvis. They are about one and a quarter inches long, three-quarters of an inch wide, and half an inch thick, and they are connected at the upper end to one of the fimbriæ of the Fallopian tubes. They contain many Graafian follicles embedded in a fibrous tissue, with each follicle housing an ovum about ¹/₁₂₅ inch in diameter, which is barely visible to the naked eye. When a follicle bursts and releases an ovum, a yellow spot called the corpus luteum appears where it ruptured. After a normal menstrual cycle, it's referred to as the false corpus luteum, and after conception, it's called the true corpus luteum, which is larger and lasts longer.

Fig. 65.—View of the pelvis and its organs. (Savage.) B, Bladder; U, uterus (drawn down by loop e); F, Fallopian tubes; O, ovaries; L, round ligaments; g, ureter; a, ovarian vessels, often prominent under their peritoneal covering; R, rectum; V, vertebra.

Fig. 65.—View of the pelvis and its organs. (Savage.) B, Bladder; U, uterus (pulled down by loop e); F, Fallopian tubes; O, ovaries; L, round ligaments; g, ureter; a, ovarian vessels, often noticeable under their peritoneal covering; R, rectum; V, vertebra.

The Fallopian tubes are the oviducts and convey the ova from the ovaries to the uterus. They are four inches long and lie between the layers of the broad ligaments, opening into the uterus by an orifice the [Pg 167] size of a bristle, while the end next to the ovary spreads out trumpet-like and is edged with fimbriæ as with a fringe, the fimbriated extremity. There are three coats: a serous coat which is continuous with the peritoneum, a muscular coat, and, within, a mucous coat covered with cilia, continuous with the mucous membrane of the uterus. One fimbria is attached to the ovary and as the ovum is given off it finds its way into the tube and thence to the uterus.

The Fallopian tubes are the oviducts that transport the eggs from the ovaries to the uterus. They are four inches long and sit between the layers of the broad ligaments, opening into the uterus through a tiny opening the size of a bristle, while the end nearest the ovary flares out like a trumpet and has fringes called fimbriæ, which are the fimbriated tips. There are three layers: an outer serous layer that merges with the peritoneum, a muscular layer, and an inner mucous layer covered with tiny cilia, that connects with the mucous membrane of the uterus. One fimbria is attached to the ovary, and as the egg is released, it makes its way into the tube and then to the uterus.

Fig. 66.—Sagittal section of the female pelvis.
(Dickinson.)

Fig. 66.—Sagittal section of the female pelvis.
(Dickinson.)

The uterus is a pear-shaped organ, about three inches long, two inches broad above, and one inch thick, situated in the pelvic cavity between the rectum and the bladder. The wide part or fundus is above [Pg 168] and the narrow neck or cervix below, lying partly within the vagina. The whole is held in place by ligaments. These include the broad ligaments, which extend from the sides of the uterus to the lateral walls of the pelvis, and the round ligaments, two muscular cords, about four inches long, which pass out through the abdominal ring into the inguinal canal and so to the mons veneris and labia, thus corresponding to the spermatic cords in the male. The cavity of the body of the uterus is small and flattened and opens into the cervix by the internal os uteri, the external os being at the opening of the cervix into the vagina. There are three coats: a serous coat derived from the peritoneum, a muscular coat of unstriped fibers which forms the bulk of the whole organ, and a mucous coat covered with ciliated epithelium.

The uterus is a pear-shaped organ, about three inches long, two inches wide at the top, and one inch thick, located in the pelvic cavity between the rectum and the bladder. The wider part, called the fundus, is at the top, and the narrower neck, known as the cervix, is at the bottom, partly located within the vagina. It is held in place by ligaments. These include the broad ligaments, which extend from the sides of the uterus to the side walls of the pelvis, and the round ligaments, which are two muscular cords about four inches long that extend through the abdominal ring into the inguinal canal and then to the mons veneris and labia, similar to the spermatic cords in males. The cavity of the uterus is small and flattened, opening into the cervix through the internal os uteri, while the external os is at the opening of the cervix into the vagina. There are three layers: a serous layer derived from the peritoneum, a muscular layer made up of smooth fibers that forms most of the organ, and a mucous layer lined with ciliated epithelium.

The uterus is always enlarged during menstruation and is enormously enlarged in pregnancy. It receives the fecundated ovum, retains and supports it during the development of the fetus, and is the chief agent of expulsion. In tubal or extra-uterine pregnancy the ovum becomes attached in the tube instead of in the uterus, and develops there, rupturing the tube and causing serious hemorrhage.

The uterus always gets bigger during menstruation and expands significantly during pregnancy. It receives the fertilized egg, holds and supports it while the fetus develops, and is the main organ responsible for expulsion. In tubal or extra-uterine pregnancy, the egg attaches in the fallopian tube instead of the uterus and grows there, leading to the rupture of the tube and causing severe bleeding.

The passage from the cervix out of the body is the vagina, a membranous canal, curved upward and backward to conform to the axis of the pelvis, and attached above to the cervix. Ordinarily the sides are in contact.

The passage from the cervix out of the body is the vagina, a flexible tube that curves upward and backward to fit the shape of the pelvis and is connected at the top to the cervix. Normally, the sides are touching.

The arteries of the internal organs of generation are the uterine from the internal iliac and the ovarian from the aorta in the female, the pudic branches of the internal iliac and the spermatic from the aorta in the male. The nerves are largely from the sympathetic system.

The arteries supplying the internal reproductive organs are the uterine arteries branching from the internal iliac in females and the ovarian arteries from the aorta. In males, they are the pudendal branches of the internal iliac and the spermatic arteries from the aorta. The nerves mainly come from the sympathetic nervous system.

Abscess formation occurs frequently in the tubes and gonorrheal infection may spread up the vagina and through the uterus to the tubes, and even to the abdominal cavity itself. The tubes may also be tubercular. [Pg 169]

Abscess formation happens often in the fallopian tubes, and gonorrheal infection can move up through the vagina and uterus to the tubes, potentially reaching the abdominal cavity. The tubes might also be tubercular. [Pg 169]

Salpingectomy or removal of the tubes is the commonest operation after that for appendicitis. Cancer of the uterus may necessitate panhysterectomy or removal of the uterus and all its appendages.

Salpingectomy or the removal of the fallopian tubes is the most common surgery after appendicitis. Cancer of the uterus may require a panhysterectomy or the removal of the uterus and all its attached structures.

Fig. 67.—Virginal vulva. (Modified from Tarnier.) 1, labia majora; 2, fourchette; 3, labia minora; 4, glans clitoridis; 5, meatus urinarius; 6, vestibule; 7, entrance to the vagina; 8, hymen; 9, orifice of Bartholin’s gland; 10, anterior commissure of labia majora; 11, anus; 12, blind recess; 13, fossa navicularis; 14, body of clitoris.

Fig. 67.—Virginal vulva. (Adapted from Tarnier.) 1, outer lips; 2, perineal ridge; 3, inner lips; 4, clitoral glans; 5, urinary opening; 6, vaginal opening; 7, entrance to the vagina; 8, hymen; 9, opening of Bartholin’s gland; 10, front join of outer lips; 11, anus; 12, blind pouch; 13, navicular fossa; 14, body of the clitoris.

The external genitalia in the female, as in the male, are situated over the pubic arch. They are known as the vulva and include the mons Veneris, the labia majora and minora, the vaginal orifice, the clitoris, and the meatus urinarius.

The external genitalia in females, like in males, are located above the pubic arch. They are called the vulva and consist of the mons Veneris, the labia majora and minora, the vaginal opening, the clitoris, and the urinary opening.

The mons Veneris is a rounded eminence composed of fatty tissue, which surmounts the pubic bones and is covered with hair at puberty. From it two prominent longitudinal folds of skin, covered with hair on the outside, the labia majora, extend backward, forming the [Pg 170] lateral boundaries of the vulva. Within these labia again are two thin cutaneous folds, the labia minora or nymphæ, which run back from the clitoris for about one and a half inches and enclose the vaginal orifice. The clitoris corresponds to the penis and is just above the upper part of the labia minora. Between it and the vagina is the meatus urinarius. The orifice of the vagina is partly closed in the virgin by the hymen, a thin fold of mucous membrane, which occasionally closes it completely, imperforate hymen. The fourchette is a small transverse fold of skin at the junction of the labia minora posteriorly. Between the vagina and the rectum is the perineal body, a somewhat triangular structure made up of many small muscles. Its surface is known as the perineum. It is frequently torn wholly or in part during childbirth and has to be sewed up.

The mons Veneris is a rounded area made up of fatty tissue that sits above the pubic bones and gets covered in hair when puberty starts. From this area, two noticeable longitudinal folds of skin, which are hairy on the outside, the labia majora, stretch back, forming the lateral edges of the vulva. Inside these labia, there are two thin skin folds, the labia minora or nymphæ, which extend from the clitoris for about one and a half inches and surround the vaginal orifice. The clitoris corresponds to the penis and is located just above the upper part of the labia minora. Between it and the vagina is the meatus urinarius. The vaginal opening is partially closed in a virgin by the hymen, a thin fold of mucous membrane that can sometimes close it completely, referred to as an imperforate hymen. The fourchette is a small transverse fold of skin at the back junction of the labia minora. Between the vagina and the rectum lies the perineal body, a somewhat triangular shape made of many small muscles. Its surface is called the perineum. It often tears completely or partially during childbirth and needs to be stitched up.


CHAPTER XII.
THE ARMS.

The upper extremities include the shoulders, arms, forearms, wrists, and hands and contain each thirty-two bones. The bones of the two shoulders taken together are called the shoulder girdle and consist of the two clavicles or collar bones and the two scapulæ or shoulder blades, which together make an almost complete girdle of the shoulders.

The upper limbs consist of the shoulders, arms, forearms, wrists, and hands, featuring a total of thirty-two bones. The bones in both shoulders together are known as the shoulder girdle, which includes the two clavicles (collarbones) and the two scapulae (shoulder blades), forming an almost complete girdle for the shoulders.

The clavicle is a long slender bone extending almost horizontally from the sternum to the scapula and can be felt for its whole length in the living. For the inner two-thirds it is convex anteriorly, for the outer third concave. In woman it is generally less curved, smoother, and more slender than in man, and as bone is rough when the muscles attached are powerful, the right clavicle, being used more, is generally rougher and thicker than the left. Among the muscles attached are the large neck muscle, the sterno-cleido-mastoid, whose tendons form the presternal notch, the trapezius, the pectoralis major, and the deltoid.

The clavicle is a long, slender bone that runs almost horizontally from the sternum to the scapula and can be felt along its entire length in a living person. For the inner two-thirds, it is curved outward on the front side, while the outer third is curved inward. In women, it is usually less curved, smoother, and more slender than in men. Since bone appears rough when the muscles attached to it are strong, the right clavicle, which is used more often, tends to be rougher and thicker than the left. Among the muscles attached are the large neck muscle, the sterno-cleido-mastoid, whose tendons create the presternal notch, the trapezius, the pectoralis major, and the deltoid.

Being slender and superficial the clavicle is most frequently broken of any bone in the body, generally by indirect violence, as by falling with the hand out, though old people in such a case are apt to get Colles’ fracture at the wrist. The bone generally gives way at the juncture of the outer and middle thirds, with displacement of the parts inward, so that the fracture is seldom compound. Since, however, the main vessels of the upper arm, with their nerves, lie beneath the clavicle, there is danger of their being punctured. Such serious injury is guarded against by the presence of the subclavius muscle. The clavicle is occasionally removed for sarcoma. [Pg 172]

Being slender and superficial, the clavicle is the most commonly broken bone in the body, usually due to indirect force, like falling with your hand outstretched. However, older people in such cases are more likely to suffer a Colles’ fracture at the wrist. The bone usually breaks at the junction of the outer and middle thirds, with the broken parts shifting inward, making compound fractures rare. However, since the main blood vessels and nerves of the upper arm run beneath the clavicle, there’s a risk of them being punctured. This serious injury is mitigated by the presence of the subclavius muscle. The clavicle is sometimes removed to treat sarcoma. [Pg 172]

Fig. 68.—Bones of the upper extremity.
(Toldt.)

Fig. 68.—Bones of the upper limb.
(Toldt.)

Fig. 69.—Left scapula, posterior surface
(after Toldt).

Fig. 69.—Left shoulder blade, back side
(after Toldt).

The scapula or shoulder blade, so called from its shape, is a large, flat, triangular bone with a prominent ridge, the spine, crossing its dorsum or posterior surface near its upper edge. It extends from the second to the seventh rib, with its posterior margin parallel to and about one inch from the dorsal vertebræ. The head, in which is situated the glenoid cavity for articulation with the humerus or upper arm bone, is surrounded by a slight constriction, the neck. Above it projects the coracoid process, so called from its fancied resemblance to a crow’s beak. This can usually be felt about one inch from the juncture of the outer and middle thirds of the clavicle and from it arise the short head of the biceps and the coraco-brachialis muscle. The acromion process at the end of the spine extends out beyond the glenoid cavity posteriorly and affords [Pg 174] attachment to the deltoid and trapezius muscles. It forms the summit of the shoulder. Numerous other muscles are attached to the surface of the scapula, the only parts which are truly subcutaneous being the whole length of the spine and the acromion process, though the lower angle and the coracoid process can generally be felt. The muscles bulge so much that the spine in the living appears as a slight depression extending back almost to the vertebræ. The large number of the muscles on the shoulder and arm is due to the great flexibility and strength required for the various uses to which the arms are put.

The scapula or shoulder blade, named for its shape, is a large, flat, triangular bone with a noticeable ridge, the spine, running across its back or posterior surface near the top edge. It stretches from the second to the seventh rib, with its back edge parallel to and about one inch away from the dorsal vertebrae. The head, which contains the glenoid cavity for connecting with the humerus or upper arm bone, is surrounded by a slight narrowing called the neck. Above it juts out the coracoid process, named because it looks a bit like a crow’s beak. This is typically felt about one inch from where the outer and middle sections of the clavicle meet, and from it arise the short head of the biceps and the coraco-brachialis muscle. The acromion process at the end of the spine extends out beyond the glenoid cavity toward the back and serves as an attachment point for the deltoid and trapezius muscles. It forms the peak of the shoulder. Many other muscles attach to the surface of the scapula, the only areas that are truly close to the skin being the entire length of the spine and the acromion process, although the lower angle and the coracoid process can usually be felt. The muscles are so prominent that the spine appears as a slight depression that runs back almost to the vertebrae in living individuals. The large number of muscles on the shoulder and arm is due to the significant flexibility and strength needed for the various activities the arms perform.

Shoulder Muscles.—The most important shoulder muscle is the deltoid, a large triangular muscle, which surrounds and protects the shoulder-joint and gives the shoulder its rounded form. It rises from the outer third of the clavicle, from the acromion process, and from the whole length of the spine of the scapula, and is inserted by a tendon into a rough prominence on the middle of the outer side of the humerus. It serves to raise the arm and to draw it somewhat forward or back, according as the anterior or posterior fibers are used. The pectoralis major rises from the inner half of the clavicle, the front of the sternum, and the cartilages of the true ribs and its fibers converge to form a fan-shaped muscle, which is inserted by a flat tendon into the edge of the bicipital groove on the humerus. It draws the arm forward and inward and helps considerably in forced inspiration. The serratus magnus rises from the outer surface and upper border of the eight upper ribs and from an aponeurosis covering the upper intercostal spaces, and is inserted along the whole length of the posterior border of the scapula. It carries the scapula forward and is used in pushing.

Shoulder Muscles.—The main shoulder muscle is the deltoid, a large triangular muscle that surrounds and protects the shoulder joint and gives the shoulder its rounded shape. It originates from the outer third of the clavicle, from the acromion process, and from the entire length of the spine of the scapula, and is attached by a tendon to a rough bump on the middle of the outer side of the humerus. It helps lift the arm and move it slightly forward or backward, depending on whether the anterior or posterior fibers are engaged. The pectoralis major originates from the inner half of the clavicle, the front of the sternum, and the cartilages of the true ribs, and its fibers come together to form a fan-shaped muscle that is attached by a flat tendon to the edge of the bicipital groove on the humerus. It pulls the arm forward and inward and plays a significant role in forced breathing. The serratus magnus originates from the outer surface and upper edge of the eight upper ribs and from an aponeurosis covering the upper intercostal spaces, and is attached along the entire length of the back edge of the scapula. It moves the scapula forward and is used for pushing.

The scapula is seldom broken because it is quite movable and is covered with large muscles and because it lies on the chest, which serves as an elastic cushion. The acromion process is the part most [Pg 175] frequently broken and occasionally the neck is fractured. Tumors occur and may necessitate the amputation of the whole upper extremity.

The scapula is rarely broken because it’s very mobile and is surrounded by large muscles. Plus, it rests on the chest, which acts as a sort of cushion. The acromion process is the part that is most often broken, and sometimes the neck gets fractured. Tumors can develop and might require the amputation of the entire upper limb.

The Humerus.—The bone of the upper arm, the humerus, is the largest bone in the upper extremity and articulates with the scapula above and with the ulna and radius below. At its upper end are the head and the anatomical neck, with the greater tuberosity external to and the lesser tuberosity in front of them. The constriction of the surgical neck is below the tuberosities, and extending from between them downward and inward along the upper third of the bone is the bicipital groove for the long head of the biceps. Though round above, below the shaft becomes flattened from before backward and curves slightly forward, terminating in the internal and external condyles, from the former of which the flexors and the round pronator arise and from the latter the extensors and supinators. From the external condyle also there projects in front the radial head or capitellum for articulation with the radius. Internally to the capitellum in front and in a corresponding position on the back of the bone are the trochlear surfaces for articulation with the ulna, there being a depression in front called the coronoid fossa for the reception of the coronoid process of the ulna in flexion of the forearm, and another depression behind, the olecranon fossa, to receive the tip of the olecranon process during extension. On the lower half of the humerus at the back is the spiral groove for the musculo-spiral nerve and the superior profunda artery, while the ulnar nerve runs in a groove back of the internal condyle.

The Humerus.—The humerus is the bone in the upper arm and is the largest bone in the upper limb. It connects to the scapula at the top and to the ulna and radius at the bottom. At the upper end are the head and the anatomical neck, with the greater tuberosity on the outside and the lesser tuberosity in front of them. The narrow section of the surgical neck is located below the tuberosities, and extending between them downwards and inwards along the upper third of the bone is the bicipital groove for the long head of the biceps. While it is round at the top, below the shaft becomes flattened from front to back and curves slightly forward, ending in the internal and external condyles. From the internal condyle, the flexors and the round pronator originate, and from the external condyle, the extensors and supinators come from. From the external condyle, the radial head or capitellum projects forward for connection with the radius. Internally to the capitellum in front and in a corresponding spot on the back of the bone are the trochlear surfaces for connection with the ulna. There is a depression in front called the coronoid fossa that accommodates the coronoid process of the ulna when the forearm is flexed, and another depression at the back, the olecranon fossa, that holds the tip of the olecranon process during extension. On the lower half of the humerus at the back, there is a spiral groove for the musculo-spiral nerve and the superior profunda artery, while the ulnar nerve runs in a groove behind the internal condyle.

The humerus is almost completely covered with muscles, the only part that is subcutaneous being a small portion of the external and internal condyles. The head can be felt under the muscles and the greater tuberosity forms the point of the shoulder. When the arm is at the side, the biceps appears at the front and inner side and the brachialis [Pg 176] anticus on either side below, while on the back of the arm, with its largest swelling above, is the triceps.

The humerus is mostly covered with muscles, with only a small part of the external and internal condyles being under the skin. You can feel the head beneath the muscles, and the greater tuberosity is what forms the point of the shoulder. When the arm is at the side, you can see the biceps at the front and inner side, and the brachialis [Pg 176] anticus is on either side below, while on the back of the arm, the triceps has its largest bulge at the top.

Fig. 70.

Fig. 70.

Fig. 70.—Superficial muscles of shoulder and arm (from before): 1, Pectoralis major; 2, deltoid; 3, biceps brachii; 4, brachialis anticus; 5, triceps; 6, pronator radii teres; 7, flexor carpi radialis; 8, palmaris longus; 9, flexor carpi ulnaris; 10, supinator longus; 11, extensor ossis metacarpi pollicis; 12, extensor brevis pollicis; 13, flexor sublimis digitorum; 14, flexor longus pollicis; 15, flexor profundus digitorum; 16, palmaris brevis; 17, abductor pollicis. (Dorland’s Dictionary.)

Fig. 70.—Superficial muscles of the shoulder and arm (viewed from the front): 1, Pectoralis major; 2, deltoid; 3, biceps brachii; 4, brachialis anterior; 5, triceps; 6, pronator teres; 7, flexor carpi radialis; 8, palmaris longus; 9, flexor carpi ulnaris; 10, supinator; 11, extensor pollicis longus; 12, extensor pollicis brevis; 13, flexor digitorum superficialis; 14, flexor pollicis longus; 15, flexor digitorum profundus; 16, palmaris brevis; 17, abductor pollicis. (Dorland’s Dictionary.)

Fig. 71.

Fig. 71.

Fig. 71.—Superficial muscles of shoulder and arm (from behind): 1, Trapezius; 2, deltoid; 3, rhomboideus major; 4, infraspinatus; 5, teres minor; 6, teres major; 7, latissimus dorsi; 8, triceps; 9, anconeus; 10, brachialis anticus; 11, supinator longus; 12, extensor carpi radialis longior; 13, extensor carpi radialis brevior; 14, extensor communis digitorum; 15, extensor carpi ulnaris; 16, flexor carpi ulnaris; 17, extensor ossis metacarpi pollicis; 18, extensor brevis pollicis; 19, tendon of extensor longus pollicis. (Dorland’s Dictionary.)

Fig. 71.—Superficial muscles of the shoulder and arm (from behind): 1, Trapezius; 2, Deltoid; 3, Rhomboid Major; 4, Infraspinatus; 5, Teres Minor; 6, Teres Major; 7, Latissimus Dorsi; 8, Triceps; 9, Anconeus; 10, Brachialis Anterior; 11, Supinator Longus; 12, Extensor Carpi Radialis Longus; 13, Extensor Carpi Radialis Brevis; 14, Extensor Communis Digitorum; 15, Extensor Carpi Ulnaris; 16, Flexor Carpi Ulnaris; 17, Extensor of the Metacarpal Bone of the Thumb; 18, Extensor Brevis of the Thumb; 19, Tendon of the Extensor Longus of the Thumb. (Dorland’s Dictionary.)

Upper Arm Muscles.—The biceps is the most important arm muscle. It rises by a short head from the coracoid process of the scapula and by a long head from a tubercle on the upper margin of the glenoid cavity, the tendon arching over the head of the humerus and descending in the bicipital groove. It is inserted into the back of the tuberosity of the radius and by a broad aponeurosis into the fascia of the forearm. It flexes and supinates the forearm and renders the fascia [Pg 177] tense. Its inner border forms a guide in tying the brachial artery, as this artery runs along its inner side.

Upper Arm Muscles.—The biceps is the most important arm muscle. It has a short head that starts from the coracoid process of the scapula and a long head that begins from a tubercle on the upper edge of the glenoid cavity. The tendon curves over the head of the humerus and goes down into the bicipital groove. It attaches to the back of the radius's tuberosity and through a broad aponeurosis to the fascia of the forearm. It helps flex and rotate the forearm outward, making the fascia tight. Its inner edge serves as a reference point for tying off the brachial artery, which runs along its inner side. [Pg 177]

The brachialis anticus rises from the lower half of the outer and inner surfaces of the humerus and is inserted into the coronoid process of the ulna, thus covering and projecting the elbow-joint anteriorly. It is a flexor of the forearm.

The brachialis anticus originates from the lower half of the outer and inner surfaces of the humerus and attaches to the coronoid process of the ulna, effectively covering and extending the elbow joint at the front. It functions as a flexor of the forearm.

Another smaller muscle on the anterior arm, which also aids in flexion, is the coraco-brachialis, which extends from the coracoid process of the scapula to the middle of the inner surface of the humerus.

Another smaller muscle in the front of the arm that helps with flexion is the coraco-brachialis, which runs from the coracoid process of the scapula to the middle of the inner surface of the humerus.

Extending the entire length of the posterior surface of the humerus is the triceps, similar to the quadriceps extensor in the thigh and direct antagonist to the biceps and brachialis anticus muscles. It rises by a long head from below the glenoid fossa, by the external head from the upper third of the posterior surface of the humerus, and by the internal head from the middle and lower thirds of the posterior surface. It is inserted in the olecranon process of the ulna and serves to extend the forearm and arm.

Extending the whole length of the back surface of the humerus is the triceps, which is similar to the quadriceps muscle in the thigh and works directly against the biceps and brachialis muscles. It originates with a long head from below the glenoid fossa, from the external head at the upper third of the back surface of the humerus, and from the internal head at the middle and lower thirds of the back surface. It attaches to the olecranon process of the ulna and is responsible for extending the forearm and arm.

The humerus is more often fractured by muscular action than any other bone. Usually the fracture occurs in the lower half of the bone and sometimes the musculo-spiral nerve is involved. There is a great tendency to non-union, probably due to interposition of soft parts. Sometimes the break is across and down between the condyles, T-fracture. Involvement of the elbow-joint is more serious than fracture of the humerus alone. Sarcoma of the humerus does occur and may require the removal of the clavicle and scapula as well as of the arm bone itself. In amputation of the humerus in children a long skin flap is left to allow for growth of the bone, as it is liable to grow again.

The humerus is more frequently fractured by muscle movement than any other bone. Typically, the fracture happens in the lower half of the bone, and sometimes it affects the musculo-spiral nerve. There is a significant tendency for non-union, likely due to soft tissue getting in the way. Occasionally, the fracture runs across and down between the condyles, known as a T-fracture. Damage to the elbow joint is more serious than a fracture of the humerus by itself. Sarcoma of the humerus can happen and might require removing the clavicle and scapula, as well as the arm bone itself. In amputation of the humerus in children, a long skin flap is left to allow for the growth of the bone, since it is likely to grow back.

The Ulna.—In the forearm there are two bones, the ulna and the radius, of which the former is the longer. The ulna is on the inner side of the forearm and its upper end forms the greater part of the [Pg 178] articulation with the humerus, as most of the articulation at the wrist is formed by the radius and the inter-articular fibro-cartilage. The head of the ulna is at the lower extremity of the bone and articulates on the outer side with the radius and below with the triangular fibro-cartilage. From its inner side projects the styloid process. The olecranon process forms the upper extremity and presents anteriorly an articular surface, the greater sigmoid cavity, for articulation with the trochlea of the humerus, where it fits into the olecranon fossa during extension. The same articulating surface also covers the coronoid process, a smaller projection below and in front of the olecranon, which fits into the coronoid fossa during flexion. Continuous with the greater sigmoid cavity on the outer side is the lesser sigmoid cavity for articulation with the head of the radius. Under the triceps tendon, which is inserted into the olecranon, is a bursa or sac of synovial membrane, such as occurs in parts where much force is brought to bear.

The Ulna.—In the forearm, there are two bones: the ulna and the radius, with the ulna being the longer one. The ulna is located on the inner side of the forearm, and its upper end makes up most of the joint with the humerus, since most of the joint at the wrist is formed by the radius and the inter-articular fibro-cartilage. The head of the ulna is at the lower end of the bone, where it connects on the outer side with the radius and below with the triangular fibro-cartilage. The styloid process projects from its inner side. The olecranon process is at the upper end and has an articular surface, the greater sigmoid cavity, for articulation with the trochlea of the humerus, fitting into the olecranon fossa during extension. This same articulating surface also covers the coronoid process, a smaller projection located below and in front of the olecranon, which fits into the coronoid fossa during flexion. Continuous with the greater sigmoid cavity on the outer side is the lesser sigmoid cavity for articulation with the head of the radius. Beneath the triceps tendon, which attaches to the olecranon, is a bursa or sac of synovial membrane, typically found in areas where a lot of force is applied.

The Radius.The radius, or spoke of the wheel, is on the outer side of the forearm and gets its name from the way it turns upon the ulna in pronation. The shaft is larger below than above and is slightly curved longitudinally for greater strength. The upper extremity or head is small and has a slightly concave upper surface for articulation with the radial head of the humerus. It articulates by its sides with the lesser sigmoid cavity and is bound to the ulna by the orbicular ligament, which runs over a smooth articular surface. Below the head is the constriction of the neck with the tuberosity for the biceps tendon to the inner side below. The lower extremity is large and forms the chief part of the wrist-joint, articulating with the semilunar and scaphoid bones of the wrist. From the lower extremity the strong conical styloid process projects externally. [Pg 179]

The Radius.The radius, or spoke of the wheel, is located on the outer side of the forearm and gets its name from how it rotates around the ulna during pronation. The shaft is thicker at the bottom than at the top and has a slight curve along its length for added strength. The upper end, or head, is small and has a slightly concave top surface to connect with the radial head of the humerus. It connects on its sides with the lesser sigmoid cavity and is attached to the ulna by the orbicular ligament, which covers a smooth area for articulation. Below the head is the narrower section called the neck, which has the tuberosity for the biceps tendon on the inner side below. The lower end is large and makes up the main part of the wrist joint, connecting with the semilunar and scaphoid bones of the wrist. From the lower end, the strong conical styloid process extends outward. [Pg 179]

Fig. 72.—Bones of the right forearm
in a position of supination. (Toldt.)

Fig. 72.—Bones of the right forearm
in a position of supination. (Toldt.)

In the living the olecranon process of the ulna is always felt at the elbow and the posterior border of the ulna forms the prominent ridge down the forearm, leading to the styloid process. The head of the radius is felt just below the external condyle and often makes a dimple in the muscles of the forearm. The rest of its upper half is concealed with muscles, but the lower half is easily felt as there are only tendons over it. The styloid process is felt externally. Normally that [Pg 180] of the radius is a little lower than that of the ulna, so that in cases of fracture their relative position is of considerable importance as showing the amount of deformity.

In a living person, the olecranon process of the ulna can always be felt at the elbow, and the back edge of the ulna creates a noticeable ridge down the forearm, leading to the styloid process. The head of the radius can be felt just below the external condyle and often creates a dimple in the forearm muscles. The rest of its upper half is covered by muscles, but the lower half is easy to feel since only tendons sit on top of it. The styloid process can be felt from the outside. Typically, the styloid process of the radius is slightly lower than that of the ulna, so in cases of fracture, their relative positions are very important for indicating the degree of deformity.

The two forearm bones are more frequently broken together than separately and generally by direct violence, the lower fragment being usually drawn up by the action of the flexor and extensor muscles and producing a swelling on the palmar surface of the forearm. Indirect violence usually causes fracture of the radius only. In both cases, but especially in fracture of both bones, there is a tendency for membrane to get between the fragments, so the arm is put up in splints with the hand midway between pronation and supination in order to separate the bones as far as possible. Care must be taken not to have the bandage too tight or gangrene of the fingers may result. In most fractures of the arm it is put up bent, but in fracture of the olecranon it is put up fully extended, as the fragment is sure otherwise to be displaced by the pull of the triceps. In fact, the olecranon is sometimes fractured by the muscular force of the triceps, though usually its fracture, which is frequent, is due to direct violence. The ulna is also often fractured in the middle by direct violence or the styloid process may be broken. Fracture of the neck or shaft of the radius is very common, the most important arm fracture being that of the lower end of the radius or Colles’ fracture. This and the corresponding fracture in the leg, Pott’s fracture, are two of the commonest fractures. In dislocation of the wrist the normal relation of the two styloid processes remains unchanged, but in Colles’ fracture the lower fragment often projects on the back of the hand, making a typical deformity called the silver fork deformity.

The two forearm bones are more often broken together than separately, usually due to direct impact. The lower fragment typically gets pulled up by the action of the flexor and extensor muscles, causing swelling on the palm side of the forearm. Indirect impact usually results in a fracture of only the radius. In both situations, especially with fractures of both bones, there's a tendency for soft tissue to get caught between the fragments, so the arm is placed in splints with the hand positioned halfway between pronation and supination to keep the bones as separated as possible. Care should be taken not to make the bandage too tight, as that could lead to gangrene in the fingers. Most arm fractures are treated with the arm bent, but in the case of fracture of the olecranon, it is kept fully extended to prevent displacement from the pull of the triceps. Actually, the olecranon can sometimes fracture due to the force of the triceps muscle, although its fracture is frequently the result of direct impact. The ulna can also often be fractured in the middle due to direct impact, or the styloid process may be broken. Fractures of the neck or shaft of the radius are very common, with the most significant arm fracture being that of the lower end of the radius, known as Colles’ fracture. This, along with the corresponding fracture in the leg, Pott’s fracture, are among the most common fractures. In dislocation of the wrist, the normal alignment of the two styloid processes stays the same, but in Colles’ fracture, the lower fragment often bulges on the back of the hand, creating a characteristic deformity known as the silver fork deformity.

The bones of the wrist and hand had best be described before the forearm muscles are taken up, as the muscles of the forearm are distributed largely to the fingers.

The bones of the wrist and hand should be described before we talk about the forearm muscles, since the forearm muscles mainly connect to the fingers.

The Wrist.—The wrist or carpus is made up of [Pg 181] eight bones arranged in two rows of four each. In the first row are the scaphoid and semilunar bones, on the outer side, articulating with the radius, the cuneiform articulating with the fibro-cartilage of the wrist-joint, and the pisiform. In the second row, in corresponding positions, are the trapezium, trapezoid, os magnum, and unciform. The eminence felt on the radial side of the wrist is the protuberance of the scaphoid, while the pisiform is generally felt on the ulnar side.

The Wrist.—The wrist or carpus consists of [Pg 181] eight bones arranged in two rows of four each. In the first row are the scaphoid and semilunar bones, on the outer side, which connects with the radius, the cuneiform connecting with the fibro-cartilage of the wrist joint, and the pisiform. In the second row, in corresponding positions, are the trapezium, trapezoid, os magnum and unciform. The prominent spot felt on the radial side of the wrist is the bulge of the scaphoid, while the pisiform is usually felt on the ulnar side.

Fig. 73.—Right carpal bones, dorsal surface. T, trapezium; , trapezoid; 7, os magnum; U, unciform; S, scaphoid; L, semilunar; C, cuneiform; P, pisiform.

Fig. 73.—Right wrist bones, back surface. T, trapezium; , trapezoid; 7, capitate; U, hamate; S, scaphoid; L, lunate; C, triangular; P, pisiform.

The Hand.—The hand contains nineteen bones, five metacarpal bones, one for each finger and the thumb, whose bases articulate with the lower row of wrist bones, and fourteen phalanges, three for each finger and two for the thumb, of which the first row articulate with the metacarpal bones. They are all long bones and are slightly concave anteriorly. When the hand is flexed it is the heads of the metacarpal bones, not the bases of the phalanges, that are so prominent, the head of the third metacarpal being most prominent.

The Hand.—The hand has nineteen bones: five metacarpal bones, one for each finger and the thumb, which connect with the lower row of wrist bones, and fourteen phalanges, three for each finger and two for the thumb. The first row of phalanges connects to the metacarpal bones. All of these are long bones and slightly curved in the front. When the hand is bent, it’s the heads of the metacarpal bones that stick out the most, not the bases of the phalanges, with the head of the third metacarpal being the most noticeable.

The metacarpals are seldom fractured, though bad fractures occasionally occur. In comminuted fracture nothing can be done but remove the bone. If the periosteum is left the bone will grow again. [Pg 182] Two diseases sometimes affect the metacarpals and the phalanges, tuberculosis and syphilis. Both cause swelling of the bones.

The metacarpals are rarely fractured, but severe fractures can happen. In the case of a comminuted fracture, the only solution is to remove the bone. If the periosteum is left intact, the bone can regrow. [Pg 182] Two diseases can sometimes affect the metacarpals and the phalanges: tuberculosis and syphilis. Both lead to swelling of the bones.

Muscles of the Forearm.—The chief groups of muscles on the forearm are the flexors and pronators on the anterior surface and the extensors and supinators on the posterior surface. In general the flexors and pronators take their origin from on or around the internal condyle, while the extensors and supinators arise on or around the external condyle. Where not otherwise stated it will be understood that such is their origin. In a general way they may by grouped as follows:

Muscles of the Forearm.—The main groups of muscles in the forearm are the flexors and pronators on the front side and the extensors and supinators on the back side. Typically, the flexors and pronators originate from or near the inner condyle, whereas the extensors and supinators come from or near the outer condyle. Unless stated otherwise, this will be understood as their origin. Generally, they can be grouped as follows:

Front Surface.
Flexors of wrist flexor carpi radialis
flexor carpi ulnaris
palmaris longus
Flexors of fingers flexor sublimis digitorum
flexor profundus digitorum
Flexor of thumb   flexor longus pollicis
Pronators of hand pronator radii teres
pronator quadratus

Back Surface.
Extensor of forearm   anconeus
Extensors of wrist extensor carpi radialis longior
extensor carpi radialis brevior
extensor carpi ulnaris
Extensors of thumb extensor ossis metacarpi pollicis
extensor primi internodii pollicis
extensor secundi internodii pollicis
Extensor of fingers   extensor communis digitorum
Extensor of index finger   extensor indicis
Extensor of little finger   extensor minimi digiti
Supinators of hand supinator longus
supinator brevis

[Pg 183] Of the flexors of the wrist the flexor carpi radialis is inserted into the base of the index and usually of the third metacarpal bone, the flexor carpi ulnaris into the fifth metacarpal, the pisiform and the unciform bones, while the palmaris longus goes to the anterior annular ligament of the wrist and the palmar fascia of the hand. The flexor sublimis digitorum is inserted by four tendons into the second phalanges of the fingers, while the flexor profundus digitorum arises from the upper part of the ulna and is inserted into the last phalanges of the fingers. The flexor of the thumb arises from the middle of the radius and is inserted into the last phalanx of the thumb. Which joint is flexed by a muscle depends upon the origin and insertion of the muscle, all those included between being affected. Thus, the flexor sublimis digitorum, which has its origin in part at least from the condyle and is inserted in the second phalanges of the fingers, flexes the forearm, wrist, and all the finger-joints but the last, while the flexor profundus digitorum, arising from the ulna, though it flexes the wrist and fingers, has no power of flexing the forearm.

[Pg 183] Of the wrist flexors, the flexor carpi radialis attaches to the base of the index finger and usually the third metacarpal bone, the flexor carpi ulnaris attaches to the fifth metacarpal, the pisiform, and the unciform bones, while the palmaris longus connects to the anterior annular ligament of the wrist and the palm fascia of the hand. The flexor sublimis digitorum attaches through four tendons to the second phalanges of the fingers, while the flexor profundus digitorum originates from the upper part of the ulna and connects to the last phalanges of the fingers. The flexor of the thumb originates from the middle of the radius and attaches to the last phalanx of the thumb. Which joint is flexed by a muscle depends on where the muscle starts and ends, affecting all the joints in between. Thus, the flexor sublimis digitorum, which has part of its origin from the condyle and attaches to the second phalanges of the fingers, flexes the forearm, wrist, and all finger joints except the last, while the flexor profundus digitorum, coming from the ulna, flexes the wrist and fingers but doesn’t flex the forearm.

The pronator radii teres, besides arising from the supra-condylar ridge, rises from the coronoid process of the ulna. It is inserted into the middle of the outer surface of the radius and serves to pronate the forearm. The other pronator, the pronator quadratus, is a small quadrilateral muscle extending transversely across the radius and ulna just above their carpal extremities. It rises from the anterior surface of the ulna and is inserted into the anterior external border of the radius.

The pronator radii teres, in addition to coming from the supra-condylar ridge, also originates from the coronoid process of the ulna. It attaches to the middle of the outer surface of the radius and is responsible for pronating the forearm. The other pronator, the pronator quadratus, is a small four-sided muscle that runs horizontally across the radius and ulna just above their wrist ends. It arises from the front surface of the ulna and connects to the front outer edge of the radius.

On the back of the forearm the anconeus serves to extend the forearm only, being inserted into the upper part of the posterior surface of the ulna. The extensors of the wrist are inserted into the bases of the various metacarpal bones and have some power to extend the forearm as well as the wrist. The extensors of the thumb, as their names imply, go one to the metacarpal bone and one to each of the phalanges, [Pg 184] the longest one extending the whole thumb, the others only a part. They rise from the ulna and radius, not the condyle. The extensor communis digitorum goes to all the phalanges of all the fingers, the extensor minimi digiti to those of the little finger only, and the extensor indicis to those of the index finger, the last two arising short of the condyle.

On the back of the forearm, the anconeus only functions to extend the forearm and is attached to the upper part of the back surface of the ulna. The extensors of the wrist are connected to the bases of the different metacarpal bones and can extend both the forearm and the wrist to some extent. The extensors of the thumb, as their names suggest, attach to the metacarpal bone and to each of the phalanges, [Pg 184] with the longest one extending the entire thumb and the others only part of it. They originate from the ulna and radius, not from the condyle. The extensor communis digitorum goes to all the phalanges of all the fingers, the extensor minimi digiti is for the little finger only, and the extensor indicis is for the index finger, with the last two originating before the condyle.

Of the supinators the longer one is inserted into the styloid process of the radius, while the shorter one, the supinator brevis, is inserted into the upper part of the same bone, both thus serving to turn the radius on the ulna.

Of the supinators, the longer one attaches to the styloid process of the radius, while the shorter one, the supinator brevis, connects to the upper part of the same bone, both helping to rotate the radius over the ulna.

Where the tendons of the various muscles pass over the wrist, both front and back, they are covered with a synovial sheath and are held down by a broad ligament, which some of them perforate, the annular ligament. The strong fibrous band of the anterior annular ligament arches over the carpal bones in front. Beneath it pass the median nerve and the tendons of the flexors of the fingers and thumb. The posterior annular ligament is of less importance.

Where the tendons of different muscles pass over the wrist, both in the front and back, they're covered by a synovial sheath and secured by a broad ligament, which some of them go through, called the annular ligament. The strong fibrous band of the anterior annular ligament arches over the carpal bones in the front. Beneath it, the median nerve and the tendons of the finger and thumb flexors pass. The posterior annular ligament is less significant.

The deep palmar fascia forms a sheath for the muscles of the hand. In carpenters there sometimes occurs Dupuytren’s contraction of the palmar fascia, which draws the fingers up. As operation is not always successful, it is quite a serious matter.

The deep palmar fascia creates a covering for the muscles in the hand. Carpenters sometimes develop Dupuytren’s contraction of the palmar fascia, which causes the fingers to curl up. Since surgery isn't always successful, it can be a rather serious issue.

The muscles of the hand itself include various abductor, adductor, and short flexor muscles of the thumb and little finger. There also extend between the metacarpal bones the lumbricales, four small muscles that aid the deep flexor muscles; likewise seven interossei, of which four are dorsal and three palmar. The dorsal interossei arise by two heads from the adjacent sides of the metacarpal bones and are inserted into the bases of the first phalanges, thus abducting the fingers; while the palmar interossei, arising from the palmar surface of the second, fourth, and fifth metacarpals, are inserted into the [Pg 185] three corresponding first phalanges and adduct the fingers toward an imaginary line drawn through the middle finger.

The muscles of the hand include various abductor, adductor, and short flexor muscles for the thumb and little finger. Additionally, there are lumbricales, four small muscles that support the deep flexor muscles, and seven interossei, of which four are dorsal and three are palmar. The dorsal interossei arise from two heads on the adjacent sides of the metacarpal bones and attach to the bases of the first phalanges, allowing for finger abduction. Meanwhile, the palmar interossei, originating from the palmar surface of the second, fourth, and fifth metacarpals, are connected to the [Pg 185] three corresponding first phalanges and pull the fingers towards an imaginary line drawn through the middle finger.

Joints of the Upper Extremity.—The joints of the upper extremity, with the exception of the wrist-joint, are the most freely movable of any in the body, probably because the hand has the finest work to do and a greater number of motions are required. Even the wrist has much greater freedom of motion than the corresponding joint in the lower extremity.

Joints of the Upper Extremity.—The joints in the upper body, except for the wrist joint, are the most flexible in the entire body, likely because the hand needs to perform intricate tasks and requires a wide range of movements. Even the wrist allows for much more movement than the equivalent joint in the lower body.

The shoulder-joint is rather a deep joint, to allow of the varied motion required, and has a capsular ligament from the margin of the glenoid fossa above to the neck of the humerus below. The elbow, which is a hinge joint, has an anterior and a posterior ligament and two lateral ligaments, as is practically the case in all such joints. The wrist has several ligaments which, taken together, are capsular in nature.

The shoulder joint is quite a deep joint, which allows for the various movements needed, and has a capsular ligament that goes from the edge of the glenoid fossa above to the neck of the humerus below. The elbow, which is a hinge joint, has an anterior and a posterior ligament along with two lateral ligaments, just like most such joints do. The wrist has several ligaments that, together, form a capsular structure.

Blood Supply of the Upper Extremity.—The blood supply of the upper extremity comes through the subclavian artery, which, on the right, springs from the innominate artery and on the left from the aortic arch. It remains one trunk as far as the elbow, though different names have been given to different parts. Thus, as it passes over the lower border of the first rib, it becomes the axillary, and at the lower border of the axilla, where it starts down the arm, the brachial. At the elbow it divides into the ulnar and radial arteries.

Blood Supply of the Upper Extremity.—The blood supply to the upper arm comes from the subclavian artery, which originates from the innominate artery on the right side and from the aortic arch on the left side. It stays as a single vessel until it reaches the elbow, although different sections have different names. As it crosses over the lower edge of the first rib, it turns into the axillary artery, and at the lower edge of the armpit, where it begins to travel down the arm, it becomes the brachial artery. At the elbow, it splits into the ulnar and radial arteries.

In its upper part the brachial artery lies internal to the humerus but below it is in front of the bone. The radial runs in a line from the middle of the elbow anteriorly to the inner side of the styloid process of the radius and is much exposed to injury in the lower third of its course, as when the hand is thrust through glass. On it at the wrist the pulse is counted. It is much smaller than the ulnar and winds around the outer side of the thumb to the palm, where, with the deep branch from the ulnar, it forms the deep palmar arch. The [Pg 186] ulnar artery passes obliquely inward to the middle of the forearm and thence along its ulnar border to the palm of the hand, where it divides into the deep branch and the superficial palmar arch which supplies the four digital arteries.

In its upper part, the brachial artery is located inside the humerus, but lower down, it sits in front of the bone. The radial artery runs from the middle of the elbow forward to the inner side of the styloid process of the radius and is quite vulnerable to injury in the lower third of its path, like when the hand goes through glass. The pulse is felt on it at the wrist. It's significantly smaller than the ulnar and wraps around the outer side of the thumb to the palm, where, along with the deep branch from the ulnar, it forms the deep palmar arch. The ulnar artery runs at an angle inward to the middle of the forearm and then along its ulnar edge to the palm, where it splits into the deep branch and the superficial palmar arch, which supplies the four digital arteries.

From the axillary artery branches go to the chest wall and shoulder, the most important being the two circumflex arteries to the deltoid. The brachial has only two branches of any importance, the superior and inferior profunda, both on the upper arm, of course.

From the axillary artery, branches extend to the chest wall and shoulder, with the most significant ones being the two circumflex arteries that supply the deltoid. The brachial artery has only two important branches, the superior and inferior profunda, both located in the upper arm, of course.

In case of hemorrhage compression can frequently be applied with the fingers where the subclavian crosses the rib or in the axilla, where the artery can be pressed up against the humerus.

In the event of hemorrhage, you can often apply pressure with your fingers where the subclavian artery crosses the rib or in the armpit, where the artery can be pushed against the humerus.

Nerves.—The nerve supply of the shoulder comes chiefly from the anterior and posterior thoracic, the suprascapular, and the circumflex, these last going to the deltoid. The biceps is supplied by the musculo-cutaneous, the triceps by the musculo-spiral, and the brachialis anticus by both. Most of the flexor and pronator muscles are supplied by the median, while the posterior interosseous and the musculo-spiral nerves go to the extensors and supinators. The ulnar nerve supplies the hand largely.

Nerves.—The nerve supply of the shoulder mainly comes from the anterior and posterior thoracic nerves, the suprascapular nerve, and the circumflex nerve, with the last one supplying the deltoid. The biceps is supplied by the musculo-cutaneous nerve, the triceps by the musculo-spiral nerve, and the brachialis anticus by both. Most of the flexor and pronator muscles are supplied by the median nerve, while the posterior interosseous and the musculo-spiral nerves supply the extensors and supinators. The ulnar nerve mainly supplies the hand.


CHAPTER XIII.
The legs.

The lower extremities resemble the upper very closely in the arrangement of the bones, muscles, arteries, and nerves, though modifications occur, due to the difference in function of the lower limbs. There is one long bone in the upper part or thigh, the femur, and two in the lower part or leg, the tibia and fibula, while over the knee-joint is the patella or knee-cap. The ankle has seven bones and the foot nineteen like the hand.

The lower limbs are very similar to the upper limbs in how the bones, muscles, arteries, and nerves are organized, although there are some changes due to the different functions of the legs. There’s one long bone in the upper part or thigh, called the femur, and two in the lower part or leg, the tibia and fibula, while the knee has the patella or kneecap. The ankle has seven bones, and the foot has nineteen, just like the hand.

The Femur.The femur is the longest bone in the body, being about one-fourth the height of the person. It inclines toward its fellow at the knee in order to bring the knee-joints near the center of gravity in walking, the amount of inclination varying with the width of the hips and the height of the person. On account of the greater width of hip the tendency to knock-knee is greater in women than in men.

The Femur.The femur is the longest bone in the body, making up about one-fourth of a person's height. It angles inward at the knee to help keep the knee joints close to the center of gravity while walking, with the angle varying based on hip width and individual height. Due to their wider hips, women are more likely to have a tendency toward knock-knees compared to men.

The shaft of the femur is enlarged at the extremities and is slightly curved forward, the concavity being strengthened at the back by a longitudinal ridge, the linea aspera, along part of which the gluteus maximus muscle is attached. The head, which is covered with cartilage, except for an oval depression for the attachment of the ligamentum teres, one of the ligaments of the hip-joint, and which articulates with the hollow of the acetabulum in the os innominatum, projects considerably upward, inward, and forward from the shaft, the neck varying much in length and angle. It is generally more [Pg 188] horizontal in women than in men and in rickets the great weight on the softened bone tends to press the head down, causing the deformity known as “coxa vera”, in which the neck is almost horizontal. Extending upward, outward, and backward from the shaft at the base of the neck, about three-quarters of an inch lower than the head and about on a [Pg 189] level with the acetabulum and the spine of the os pubis, is the greater trochanter. This large, irregular prominence and the smaller one of the lesser trochanter, which is at the lower part of the base of the neck posteriorly, are for the attachment of muscles and to assist in rotating the bone. The lower extremity of the femur is larger than the upper and is flat from before backward. Between its two large eminences, the external and internal condyles, is a smooth depression in front, the trochlear surface, for articulation with the patella. The external condyle is more prominent in front, the internal inferiorly, the latter being the longer of the two by about half an inch. The epiphysis at the lower end of the femur is the only one in which ossification has begun at birth. Therefore, if ossification is found there, the child is known to have arrived at full term.

The shaft of the femur is wider at the ends and slightly curved forward, with the back reinforced by a ridge called the linea aspera, which is where the gluteus maximus muscle attaches. The head has a covering of cartilage, except for an oval indentation for the ligamentum teres, one of the ligaments in the hip joint, and it fits into the hollow of the acetabulum in the os innominatum. It extends upward, inward, and forward from the shaft, with the neck varying greatly in length and angle. Generally, it's more horizontal in women than in men, and in cases of rickets, the pressure on the softened bone pushes the head down, leading to a condition known as “coxa vera,” where the neck is nearly horizontal. Extending upward, outward, and backward from the shaft at the base of the neck, about three-quarters of an inch lower than the head and roughly in line with the acetabulum and the spine of the os pubis, is the greater trochanter. This large, irregular bump and the smaller lesser trochanter at the lower part of the neck's base at the back are sites for muscle attachment and aid in rotating the bone. The lower part of the femur is larger than the upper part and is flat from front to back. Between its two large bumps, the external and internal condyles, there’s a smooth area at the front called the trochlear surface for connecting with the patella. The external condyle sticks out more in front, while the internal one extends downwards, with the latter being about half an inch longer than the former. The epiphysis at the lower end of the femur is the only one that starts to ossify at birth. So, if ossification is present there, it indicates the child has reached full term.

Fig. 74.—Bones of the lower extremity.
(Toldt.)

Fig. 74.—Bones of the lower limb.
(Toldt.)

So many large muscles are attached to the femur that the shaft cannot be detected in the living unless the person is very thin and poorly developed. The outer surface of the greater trochanter, however, and the condyles can be felt.

So many big muscles are connected to the femur that the shaft isn't noticeable in a living person unless they're very thin and underdeveloped. However, the outer surface of the greater trochanter and the condyles can be felt.

A string stretched from the anterior superior spine of the ilium to the tuberosity of the ischium passes in the middle just over the upper edge of the greater trochanter. The line thus drawn is known as Nélaton’s line and is of considerable importance in many conditions of the hip. Thus, if the hip is dislocated, the trochanter will be thrown above Nélaton’s line, and in osteomalacia the pelvis sinks and the trochanter is again above the line.

A string stretched from the front top point of the ilium to the bump on the ischium passes right over the upper edge of the greater trochanter in the middle. The line created this way is called Nélaton’s line and is quite important in various hip conditions. For example, if the hip is dislocated, the trochanter will be above Nélaton’s line, and in osteomalacia, the pelvis sinks and the trochanter is again above the line.

Thigh Muscles.—Of the thigh muscles only a few need be mentioned. One large muscle is the psoas magnus, which has its origin on the front of the last dorsal and all the lumbar vertebræ, passes [Pg 190] down across the brim of the pelvis and under Poupart’s ligament, gradually diminishing in size, and terminates in a tendon that is inserted into the lesser trochanter. It serves to flex the thigh on the pelvis and to rotate it outward. The psoas parvus rises from the last dorsal and the first lumbar vertebræ and does not go out of the pelvis.

Thigh Muscles.—Only a few thigh muscles need to be mentioned. One important muscle is the psoas magnus, which starts at the front of the last dorsal and all the lumbar vertebrae, moves down across the top of the pelvis and under Poupart’s ligament, gradually getting smaller, and ends in a tendon that connects to the lesser trochanter. It helps to flex the thigh on the pelvis and rotate it outward. The psoas parvus originates from the last dorsal and the first lumbar vertebrae and remains within the pelvis.

The sartorius or tailor muscle is flat and ribbon-like and is the longest muscle in the body. It rises from the anterior superior spine of the ilium and is inserted into the upper inner surface of the shaft of the tibia. By it the legs are crossed. It also forms the outer side of an important landmark, Scarpa’s triangle, whose base is formed by Poupart’s ligament and the inner side by the adductor magnus muscle, which passes from the ramus of the os pubis and the tuberosity of the ischium to the linea aspera. The femoral artery bisects the triangle and runs into its apex.

The sartorius or tailor muscle is flat and ribbon-shaped and is the longest muscle in the body. It extends from the front top part of the ilium and attaches to the upper inner surface of the shaft of the tibia. It allows the legs to cross. It also forms the outer side of an important landmark, Scarpa’s triangle, which has its base created by Poupart’s ligament and its inner side by the adductor magnus muscle, running from the ramus of the pubic bone and the tuberosity of the ischium to the linea aspera. The femoral artery divides the triangle and goes into its apex.

The bulk of the anterior portion of the thigh is formed by the quadriceps extensor, which is really made up of four muscles, the rectus femoris, whose origin is on the anterior inferior iliac spine and above the acetabulum; the vastus externus, which comes from the greater trochanter and the upper linea aspera; and the vastus internus and crureus, which rise from the neck of the femur and the linea aspera. It is inserted into the tubercle of the tibia by the ligamentum patellæ, in which the patella lies. Its action is to extend the leg.

The main part of the front of the thigh is formed by the quadriceps extensor, which is really made up of four muscles: the rectus femoris, which begins at the anterior inferior iliac spine and above the acetabulum; the vastus externus, which originates from the greater trochanter and the upper linea aspera; and the vastus internus and crureus, which come from the neck of the femur and the linea aspera. It connects to the tubercle of the tibia via the ligamentum patellæ, where the patella is located. Its function is to extend the leg.

At the back and forming the buttocks are the three glutei muscles, the gluteus maximus, medius, and minimus. All these rise from the outer side of the ilium and have their insertion on or about the great trochanter. They serve to hold the trunk erect and to extend, abduct, and rotate the thigh. [Pg 191]

At the back, forming the buttocks, are the three gluteal muscles, the gluteus maximus, medius, and minimus. All of them originate from the outer side of the ilium and attach around the great trochanter. They help keep the trunk upright and allow for the extension, abduction, and rotation of the thigh. [Pg 191]

Fig. 75.

Fig. 75.

 

Fig. 76.

Fig. 76.

Fig. 77.

Fig. 77.

Fig. 75.—Superficial muscles of hip and thigh (from behind): 1, Gluteus medius; 2, gluteus maximus; 3, vastus externus; 4, biceps flexor cruris; 5, semitendinosus; 6, semimembranosus; 7, gracilis; 8, sartorius; 9, adductor magnus; 10, 11, gastrocnemius; 12, origin of plantaris. (Dorland’s Dictionary.)

Fig. 75.—Superficial muscles of the hip and thigh (viewed from behind): 1, Gluteus medius; 2, gluteus maximus; 3, vastus externus; 4, biceps femoris; 5, semitendinosus; 6, semimembranosus; 7, gracilis; 8, sartorius; 9, adductor magnus; 10, 11, gastrocnemius; 12, origin of plantaris. (Dorland’s Dictionary.)

Fig. 76.—Muscles of the inner side of thigh and interior of pelvis: 1, Iliacus; 2, psoas magnus; 3, obturator internus; 4, pyriformis; 5, erector spinæ; 6, gluteus maximus; 7, sartorius; 8, adductor longus; 9, gracilis; 10, adductor magnus; 11, semimembranosus; 12, semitendinosus; 13, rectus femoris; 14, vastus internus. (Dorland’s Dictionary.)

Fig. 76.—Muscles on the inner side of the thigh and the inside of the pelvis: 1, Iliacus; 2, psoas major; 3, obturator internus; 4, piriformis; 5, erector spinae; 6, gluteus maximus; 7, sartorius; 8, adductor longus; 9, gracilis; 10, adductor magnus; 11, semimembranosus; 12, semitendinosus; 13, rectus femoris; 14, vastus medialis. (Dorland’s Dictionary.)

Fig. 77.—Superficial muscles of front of thigh: 1, Insertion of external oblique into iliac crest; 2, aponeurosis of external oblique; 3, external abdominal ring; 4, gluteus medius; 5, tensor vaginæ formoris; 6, sartorius; 7, iliopsoas; 8, pectineus; 9, adductor longus; 10, gracilis; 11, adductor magnus; 12, vastus externus; 13, rectus femoris; 14, vastus internus; 15, biceps flexor cruris. (Dorland’s Dictionary.)

Fig. 77.—Superficial muscles of the front of the thigh: 1, Insertion of the external oblique into the iliac crest; 2, aponeurosis of the external oblique; 3, external abdominal ring; 4, gluteus medius; 5, tensor fasciae latae; 6, sartorius; 7, iliopsoas; 8, pectineus; 9, adductor longus; 10, gracilis; 11, adductor magnus; 12, vastus lateralis; 13, rectus femoris; 14, vastus medialis; 15, biceps femoris. (Dorland’s Dictionary.)

Lower down and forming the back of the thigh are the biceps and the semitendinosus and semimembranosus muscles. The biceps rises by two heads from the tuberosity of the ischium and the linea aspera and is inserted into the head of the fibula. It is on the outer side of the thigh and its tendon, which embraces the external lateral ligament of the knee-joint, forms the outer hamstring. On the inner side are the semitendinosus and the semimembranosus muscles. These rise from the tuberosity of the ischium and are inserted, the one into the upper inner surface of the shaft of the tibia and the other into the internal tuberosity of the tibia. Their tendons form the inner hamstring. Like [Pg 192] the biceps they serve to extend the thigh and flex the leg on the thigh, but where the biceps rotates the leg out they, being attached to the inner side of the leg bones, rotate it in.

Lower down, at the back of the thigh, are the biceps and the semitendinosus and semimembranosus muscles. The biceps has two heads that originate from the ischial tuberosity and the linea aspera, and it attaches to the head of the fibula. It’s located on the outer side of the thigh, and its tendon wraps around the external lateral ligament of the knee joint, forming the outer hamstring. On the inner side are the semitendinosus and semimembranosus muscles. They originate from the ischial tuberosity as well; one attaches to the upper inner surface of the tibia shaft, while the other attaches to the internal tuberosity of the tibia. Their tendons form the inner hamstring. Like the biceps, they help extend the thigh and flex the leg at the thigh, but while the biceps rotates the leg outward, these muscles, being attached to the inner side of the leg bones, rotate it inward.

The patella, or small pan, is a flat, somewhat triangular bone developed in the quadriceps extensor tendon. Four muscles are attached to it as well as the ligamentum patellæ, which holds it to the tibia and gives increased leverage by making the quadriceps extensor work at a greater angle. It articulates with the condyles and serves to protect the joint. One bursa, the prepatella bursa, separates it from the skin and another, surrounded by adipose tissue, from the head of the tibia. The external surface can be seen and felt on the front of the knee and the bone can be moved from side to side when the leg is straight.

The patella, or small patella, is a flat, somewhat triangular bone that forms in the quadriceps tendon. It has four muscles connected to it, plus the ligamentum patellæ, which anchors it to the tibia and enhances leverage by allowing the quadriceps to work at a wider angle. It connects with the condyles and helps shield the joint. One bursa, the prepatella bursa, sits between it and the skin, and another, surrounded by fat tissue, is located near the head of the tibia. The outer surface can be seen and felt at the front of the knee, and the bone can be shifted side to side when the leg is extended.

Joints of the Lower Extremity.—The hip-joint is a ball-and-socket joint but is not so freely movable as the shoulder-joint, the head of the femur being held in the acetabulum by many strong ligaments, of which the most important is the capsular ligament.

Joints of the Lower Extremity.—The hip joint is a ball-and-socket joint, but it doesn't have as much range of motion as the shoulder joint. The head of the femur is secured in the acetabulum by several strong ligaments, the most important of which is the capsular ligament.

The knee-joint is largely a hinge joint, but in some positions it has some rotation. It is formed by the condyles of the femur, the head of the tibia, and the patella, and has fourteen ligaments, including the ligamentum patellæ and the crucial ligaments. Its synovial sac is the largest found in any joint. Two semilunar cartilages, placed on the head of the tibia, serve to deepen the socket for the condyles, changing somewhat in shape and thickness as the joint moves. The interval between the thigh and the leg bones can be felt at the knee. When the leg is extended the juncture of the bones is slightly above the patella, while in flexion a knife passed below the apex of the patella will pass into the joint.

The knee-joint is mainly a hinge joint, but it allows some rotation in certain positions. It consists of the condyles of the femur, the head of the tibia, and the patella, and it has fourteen ligaments, including the ligamentum patellæ and the crucial ligaments. Its synovial sac is the largest found in any joint. Two semilunar cartilages, located on the head of the tibia, help to deepen the socket for the condyles, and they change in shape and thickness as the joint moves. You can feel the space between the thigh and leg bones at the knee. When the leg is extended, the connection of the bones is just above the patella, while in a bent position, a knife passed below the top of the patella will enter the joint.

Congenital dislocation of the hip occurs. Separation of the epiphysis of the femur may occur and sometimes the neck, rarely the lower part of the shaft, is fractured. Either condyle may be fractured off or there may be a T-fracture, in which case the popliteal [Pg 193] artery may be injured. In dislocation the head may be behind or in front of the acetabulum. Impacted hip, where the neck of the femur has, in a fall, been driven into the head, is common in old people. Sometimes, especially in young children, the bone is infected, osteomyelitis. Sarcoma occurs. Most tubercular disease of the hip originates at the upper extremity of the femur, tuberculosis generally starting in the head and then attacking the capsule and the soft parts of the joint. If neglected, shortening of the leg may result, in which case the bone has to be broken and set at an angle in order to enable the child to walk.

Congenital dislocation of the hip can happen. Separation of the epiphysis of the femur may occur, and sometimes the neck is fractured, though it’s rare for the lower part of the shaft to be affected. Either condyle can be fractured, or there may be a T-fracture, which can injure the popliteal [Pg 193] artery. In the case of dislocation, the femoral head may be positioned behind or in front of the acetabulum. Impacted hip is where the neck of the femur gets driven into the head during a fall, and this is common in older adults. Sometimes, particularly in young children, the bone can become infected, leading to osteomyelitis. Sarcoma can also develop. Most cases of tubercular disease of the hip start at the upper end of the femur, with tuberculosis usually beginning in the head and then spreading to the capsule and soft tissues of the joint. If left untreated, this can cause leg shortening, which would require breaking the bone and setting it at an angle to allow the child to walk.

Fig. 78.

Fig. 78.

Fig. 79.

Fig. 79.

Fig. 78.—Right knee-joint, posterior view. (Leidy.)

Fig. 78.—Back view of the right knee joint. (Leidy.)

Fig. 79.—Right knee-joint, showing internal ligaments: 2, anterior crucial ligament; 3, posterior crucial ligament; 4, transverse ligament; 6, 7, semilunar fibro-cartilages. (Leidy.)

Fig. 79.—Right knee joint, showing internal ligaments: 2, anterior cruciate ligament; 3, posterior cruciate ligament; 4, transverse ligament; 6, 7, semilunar fibrocartilages. (Leidy.)

Occasionally a bit of cartilage gets broken off in the knee-joint and wedged between the bones, so that the joint cannot be straightened. This is dislocation of the semilunar cartilage and necessitates an operation for removal of the piece. The cartilage will eventually be [Pg 194] replaced by fibrous tissue and in a few months the leg will be all right. Dislocation of the knee is rare, though it may occur in any direction. Often the bursæ of the joint are irritated, as by kneeling to scrub floors, and bursitis or housemaid’s knee results. Fracture of the patella may be caused by muscular traction or by direct violence, and is generally repaired by making an incision and sewing the parts of the bone together. Tumor albus or white swelling is tuberculosis of the knee and is fairly common in children. Specific knee means syphilis of the knee and generally occurs in both knees.

Sometimes a piece of cartilage breaks off in the knee joint and gets stuck between the bones, preventing the joint from straightening. This is dislocation of the semilunar cartilage and requires surgery to remove the fragment. The cartilage will eventually be replaced by fibrous tissue, and in a few months, the leg will be fine. Dislocation of the knee is rare but can happen in any direction. Often, the bursae of the joint get irritated from actions like kneeling to scrub floors, leading to bursitis or housemaid’s knee. A fracture of the patella can happen due to muscle pull or direct impact and is usually fixed by making an incision to stitch the bone parts together. Tumor albus or white swelling refers to tuberculosis of the knee and is relatively common in children. Specific knee refers to syphilis of the knee and typically affects both knees.

The Tibia.The tibia or shin bone is next longest to the femur and is on the inner side of the leg, corresponding to the ulna in the arm. The shaft is prismoid and is more slender for the lower quarter, where fracture is consequently most frequent. The anterior border forms the crest or shin and can be felt for its upper two-thirds. The lower extremity, which is smaller than the upper, articulates with the astragalus bone of the ankle and with the fibula. Its head or upper extremity is expanded into two lateral tuberositis for articulation with the femur and for muscular attachment, both of which can easily be felt just below the bend of the knee. Their upper surfaces are smooth and concave, with a vertical bifid spine in the middle and a prominent tubercle for the attachment of the semilunar cartilages on either side. On the anterior surface of the head, below, is a rough eminence or tubercle, which also can be felt. The lower part of this is for the attachment of the ligamentum patellæ, while the upper part, which is smoother, is for the bursa that is placed under the tendon to prevent friction. On the back of the outer tuberosity is a facet for the head of the fibula. At the lower end there projects downward on the inner side, overhanging the arch of the foot, the internal malleolus, the prominent part of the ankle. It is on a higher level and somewhat farther forward than the external malleolus.

The Tibia.The tibia or shin bone is the second longest bone after the femur and is located on the inner side of the leg, corresponding to the ulna in the arm. The shaft is prismoid in shape and becomes thinner in the lower quarter, where fractures are most likely to occur. The front edge forms the crest or shin and can be felt along its upper two-thirds. The lower end, which is smaller than the upper, connects with the astragalus bone of the ankle and the fibula. Its head or upper end is broadened into two lateral tuberosities for connecting with the femur and for muscle attachment, both of which can be easily felt just below the knee bend. The upper surfaces are smooth and concave, featuring a vertical bifid spine in the center and a noticeable tubercle for attaching the semilunar cartilages on both sides. On the front surface of the head, below, there is a rough bump or tubercle that can also be felt. The lower part of this bump is for the attachment of the ligamentum patellae, while the upper part, which is smoother, is for the bursa that sits under the tendon to reduce friction. On the back of the outer tuberosity, there is a facet for the head of the fibula. At the lower end, a projection on the inner side hangs over the arch of the foot, known as the internal malleolus, which is the prominent part of the ankle. It is positioned higher and slightly more forward than the external malleolus.

The Fibula.The fibula is the most slender of all the bones in [Pg 195] proportion to its length and is on the outer side of the leg. Its head is small and placed toward the back of the tibia below the knee-joint, from which it is excluded. The head articulates with the external tuberosity and has extending upward from it the styloid process. To it is attached the biceps tendon or outer hamstring. At the lower extremity of the shaft is the external malleolus, which articulates with the astragalus and forms the outer ankle. The only parts of the fibula that can be felt, besides the malleolus, which is very prominent, are the head and the lower external surface of the shaft.

The Fibula.—The fibula is the thinnest of all the bones in [Pg 195] relation to its length and is located on the outer side of the leg. Its head is small and positioned toward the back of the tibia just below the knee joint, from which it is separate. The head connects with the external tuberosity and has the styloid process extending upward from it. The biceps tendon or outer hamstring is attached to it. At the lower end of the shaft is the external malleolus, which connects with the astragalus and forms the outer ankle. The only parts of the fibula that can be felt, besides the malleolus, which is quite prominent, are the head and the lower outer surface of the shaft.

In fracture of the leg both bones are usually broken, though either may be broken separately. Pott’s fracture is fracture of the lower fibula, and may be caused by stamping hard when stepping on to the sidewalk. In rickets the tibia becomes bowed outward and forward, causing bow leg, a condition which in very young children may be rectified by manipulation. Later on braces are needed and after five years the bones have to be broken and set straight.

In fracture of the leg, both bones are usually broken, but either one can break on its own. Pott’s fracture is when the lower fibula is fractured, often caused by stepping hard onto the sidewalk. In cases of rickets, the tibia bends outward and forward, leading to bow leg, a condition that can often be corrected in very young children through manipulation. As they get older, braces are needed, and after the age of five, the bones may have to be broken and set straight.

The Ankle.—The ankle or tarsus has but seven bones where the wrist has eight. They are the os calcis or heel bone, which is the largest and strongest and forms the tuberosity of the heel; the astragalus, which is next largest and helps to form the ankle-joint; the cuboid; the navicular (boat-like) or scaphoid; and the internal, middle, and external cuneiform bones. The astragalus is above and partially in front of the os calcis, to which is attached the tendo Achillis. The cuboid is on the outer side of the foot, in front of the os calcis and behind the metatarsals. It is noticeable in congenital club-foot, in which condition the tarsal bones may be distorted in shape and misplaced. The navicular or scaphoid is on the inner side of the foot, between the astragalus and the three cuneiform bones.

The Ankle.—The ankle or tarsus has only seven bones, while the wrist has eight. These include the os calcis or heel bone, which is the largest and strongest, forming the tuberosity of the heel; the astragalus, which is the next largest and helps make up the ankle joint; the cuboid; the navicular (boat-like) or scaphoid; and the internal, middle, and external cuneiform bones. The astragalus sits above and slightly in front of the os calcis, to which the tendo Achillis is attached. The cuboid is located on the outside of the foot, in front of the os calcis and behind the metatarsals. It becomes noticeable in cases of congenital club-foot, where the tarsal bones may be misshapen and out of position. The navicular or scaphoid is found on the inner side of the foot, located between the astragalus and the three cuneiform bones.

The Foot.—There are five metatarsal bones in the foot, corresponding to the five metacarpals in the hand, and the toes have [Pg 196] the same number of phalanges as the fingers, though they are shorter and stronger. The big toe corresponds to the thumb.

The Foot.—There are five metatarsal bones in the foot, similar to the five metacarpals in the hand, and the toes have [Pg 196] the same number of phalanges as the fingers, although they are shorter and sturdier. The big toe is like the thumb.

Fig. 80.—Bones of the right foot, dorsal surface: 1, Astragalus; 2, talus; 3, os calcis, 4, navicular; 5, internal cuneiform; 6, middle cuneiform; 7, external cuneiform; 8, cuboid; 9, metatarsus; 10-14, phalanges. (Leidy.)

Fig. 80.—Bones of the right foot, top view: 1, Astragalus; 2, talus; 3, calcaneus; 4, navicular; 5, internal cuneiform; 6, middle cuneiform; 7, external cuneiform; 8, cuboid; 9, metatarsals; 10-14, phalanges. (Leidy.)

Fracture of the os calcis and the astragalus are most commonly caused by a fall from a height, while the metatarsals and phalanges are generally broken by something heavy falling upon them. Because of their delicate structure, their distance from the heart, and the differences of temperature to which they are subjected, the tarsal bones are especially liable to become tubercular, amputation of the feet even becoming necessary at times. In diabetes there may be a perforating ulcer on the sole of the foot and the bone may become diseased. [Pg 197]

Fracture of the heel bone and the ankle bone usually happens when someone falls from a height, while the metatarsals and toe bones typically get broken by something heavy falling on them. Because of their fragile structure, their distance from the heart, and the varying temperatures they experience, the tarsal bones are particularly prone to becoming tubercular, and sometimes amputation of the feet may be necessary. In diabetes, there might be a perforating ulcer on the bottom of the foot, and the bone can become unhealthy. [Pg 197]

Fig. 81.

Fig. 81.

 

Fig. 82.

Fig. 82.

Fig. 83.

Fig. 83.

Fig. 81.—Superficial muscles of the leg from inner side: 1, Vastus internus; 2, sartorius; 3, gracilis; 4, semitendinosus; 5, semimembranosus; 6, inner head of gastrocnemius; 7, soleus; 8, tendon of plantaris; 9, tendon of tibialis posticus; 10, flexor longus digitorum; 11, flexor longus hallucis; 12, tibialis anticus; 13, abductor hallucis. (Dorland’s Dictionary.)

Fig. 81.—Surface muscles of the leg from the inner side: 1, Vastus internus; 2, sartorius; 3, gracilis; 4, semitendinosus; 5, semimembranosus; 6, inner head of gastrocnemius; 7, soleus; 8, tendon of plantaris; 9, tendon of tibialis posterior; 10, flexor longus digitorum; 11, flexor longus hallucis; 12, tibialis anterior; 13, abductor hallucis. (Dorland’s Dictionary.)

Fig. 82.—Muscles of leg and foot (from before): 1, Tendon of rectus femoris; 2, vastus internus; 3, vastus externus; 4, sartorius; 5, iliotibial band; 6, inner head of gastrocnemius; 7, inner part of soleus; 8, tibialis anticus; 9, extensor proprius hallucis; 10, extensor longus digitorum; 11, peroneus longus; 12, peroneus brevis; 13, peroneus tertius; 14, origin of extensor brevis digitorum. (Dorland’s Dictionary.)

Fig. 82.—Muscles of leg and foot (from the front): 1, Tendon of the rectus femoris; 2, vastus internus; 3, vastus externus; 4, sartorius; 5, iliotibial band; 6, inner head of gastrocnemius; 7, inner part of soleus; 8, tibialis anterior; 9, extensor hallucis longus; 10, extensor digitorum longus; 11, peroneus longus; 12, peroneus brevis; 13, peroneus tertius; 14, origin of extensor digitorum brevis. (Dorland’s Dictionary.)

Fig. 83.—Superficial muscles of leg (from behind): 1, Vastus externus; 2, biceps flexor cruris; 3, semitendinosus; 4, semimembranosus; 5, gracilis; 6, sartorius; 7, outer, and 8, inner, head of gastrocnemius; 9, plantaris; 10, soleus; 11, peroneus longus; 12, peroneus brevis; 13, flexor longus digitorum; 14, tibialis posticus; 15, lower fibers of flexor longus hallucis. (Dorland’s Dictionary.)

Fig. 83.—Superficial muscles of the leg (from behind): 1, Vastus externus; 2, biceps flexor cruris; 3, semitendinosus; 4, semimembranosus; 5, gracilis; 6, sartorius; 7, outer head of gastrocnemius; 8, inner head of gastrocnemius; 9, plantaris; 10, soleus; 11, peroneus longus; 12, peroneus brevis; 13, flexor longus digitorum; 14, tibialis posterior; 15, lower fibers of flexor longus hallucis. (Dorland’s Dictionary.)

Muscles of the Leg.—The greater part of the calf of the leg is formed by the gastrocnemius, a large bulging muscle, which rises from the condyles of the femur and is inserted along with the soleus, whose origin is on the back of the upper fibula, and the plantaris, which comes from the linea aspera, into the os calcis by a common tendon, the tendo Achillis, the largest and strongest tendon in the body. Its action is to extend the foot and to rotate it slightly inward. Other extensors of the foot, which also evert it, are the peroneus longus and the peroneus brevis at the upper and outer part of the leg, the former rising from the outer tuberosity of the tibia and [Pg 198] the upper fibula and being inserted into the first metatarsal and the internal cuneiform, the latter arising from the lower fibula and being inserted into the fifth metatarsal. The foot is flexed, adducted, and rotated inward by means of the tibialis anticus, which rises from the outer tuberosity and the upper two-thirds of the outer surface of the tibia and is inserted into the internal cuneiform bone.

Muscles of the Leg.—Most of the calf muscle is made up of the gastrocnemius, a large bulging muscle that starts from the condyles of the femur and connects, along with the soleus, which originates on the back of the upper fibula, and the plantaris, which comes from the linea aspera, into the os calcis through a common tendon, the tendo Achillis, the largest and strongest tendon in the body. Its function is to extend the foot and slightly rotate it inward. Other muscles that extend the foot and also evert it are the peroneus longus and the peroneus brevis at the upper and outer part of the leg, with the former starting from the outer tuberosity of the tibia and the upper fibula and connecting to the first metatarsal and the internal cuneiform, and the latter starting from the lower fibula and connecting to the fifth metatarsal. The foot is flexed, adducted, and rotated inward by the tibialis anticus, which comes from the outer tuberosity and the upper two-thirds of the outer surface of the tibia and connects to the internal cuneiform bone.

In the foot, and corresponding to the palmar fascia in the hand, is the plantar fascia, the densest of all fibrous membranes. There are also various annular ligaments, and the foot muscles are arranged similarly to those in the hand.

In the foot, which corresponds to the palmar fascia in the hand, is the plantar fascia, the densest of all fibrous membranes. There are also several annular ligaments, and the foot muscles are organized similarly to those in the hand.

The Blood Supply of the Lower Extremity.—The blood supply of the lower extremity comes from the external iliac artery, a branch of the common iliac, which passes obliquely downward and outward along the border of the psoas muscle to Poupart’s ligament, where it enters the thigh and becomes the femoral artery. Its only important branches are the deep epigastric, which goes up along the internal abdominal ring, and the deep circumflex iliac. As the femoral artery it passes down the inner side of the thigh to the internal condyle of the femur, being very superficial at Scarpa’s triangle, where it can be compressed with the thumb to stop hemorrhage below. If a tourniquet is applied, it should be applied a little lower down. The first and most important branch of the femoral is the profunda femoris.

The Blood Supply of the Lower Extremity.—The blood supply to the lower leg comes from the external iliac artery, which branches off the common iliac and travels diagonally down and out along the edge of the psoas muscle to Poupart’s ligament. Here, it enters the thigh and becomes the femoral artery. Its only significant branches are the deep epigastric, which ascends alongside the internal abdominal ring, and the deep circumflex iliac. As the femoral artery, it continues down the inner thigh to the internal condyle of the femur, being quite superficial at Scarpa’s triangle, where it can be pressed with the thumb to stop bleeding below. If a tourniquet is needed, it should be placed slightly lower down. The first and most important branch of the femoral artery is the profunda femoris.

About two-thirds of the way to the knee the artery takes the name popliteal. It lies superficially in the popliteal space back of the knee, but above and below it is covered with muscles. Its branches supply the knee-joint and nearby muscles and are unimportant. At the lower border of the popliteus muscle, a small muscle at the knee, it divides into the anterior and posterior tibial arteries. The course of the former of these may be marked by a line from the inner side of the head of the fibula to midway between the malleoli at the front of [Pg 199] the ankle, where it terminates in the dorsalis pedis artery for the back of the foot. By this last the pulse is sometimes taken and its pulsation is a guide in determining how high up to amputate in gangrene of the foot. The posterior tibial extends obliquely down the back of the leg to the heel, where it divides into the internal and external plantar arteries which go to the sole of the foot. Its most important branch is the peroneal.

About two-thirds of the way to the knee, the artery is called the popliteal. It lies just beneath the skin in the popliteal space behind the knee, but it is covered by muscles above and below. Its branches supply blood to the knee joint and nearby muscles, but they aren't very significant. At the lower edge of the popliteus muscle, a small muscle at the knee, it splits into the anterior and posterior tibial arteries. The path of the anterior tibial artery can be traced from the inner side of the head of the fibula to halfway between the malleoli at the front of [Pg 199] the ankle, where it ends in the dorsalis pedis artery at the top of the foot. This artery is sometimes used to take a pulse, and its beat helps determine how high to amputate in cases of gangrene in the foot. The posterior tibial artery runs diagonally down the back of the leg to the heel, where it branches into the internal and external plantar arteries that lead to the sole of the foot. Its most important branch is the peroneal.

Besides the deep veins accompanying the arteries there are the superficial veins, the internal or long saphenous on the inner side of the leg and thigh and the external or short saphenous on the middle of the leg posteriorly and emptying into the popliteal vein. Varicosity often occurs in these veins.

Besides the deep veins alongside the arteries, there are the superficial veins: the internal or long saphenous on the inner side of the leg and thigh, and the external or short saphenous in the middle of the leg at the back, which empty into the popliteal vein. Varicose veins often occur in these veins.

Nerves.—The nerves of the muscles about the hip are branches of the lumbar nerve. The anterior crural supplies the anterior part of the thigh, the gluteal the muscles of the same name, and the great sciatic the large muscles of the back of the thigh. Below the knee the anterior tibial goes to the tibialis anticus and the internal popliteal to the muscles of the calf, while the peroneus muscles are supplied by the musculo-cutaneous. [Pg 200]

Nerves.—The nerves that control the muscles around the hip are branches of the lumbar nerve. The anterior crural nerve supplies the front part of the thigh, the gluteal nerve serves the gluteal muscles, and the great sciatic nerve innervates the large muscles at the back of the thigh. Below the knee, the anterior tibial nerve goes to the tibialis anterior, and the internal popliteal nerve innervates the calf muscles, while the peroneus muscles are supplied by the musculo-cutaneous nerve. [Pg 200]



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Stoney’s Materia Medica was written by a head nurse who understands exactly what nurses need. American Medicine reports that it includes “all the information about drugs that a nurse should know. * * * The treatment for poisoning is presented in a way that allows it to be carried out thoroughly and intelligently.”

Materia Medica for Nurses. By Emily M. A. Stoney, Superintendent of the Training School for Nurses in the Carney Hospital, South Boston, Mass. 12mo volume of 300 pages. Cloth, $1.50 net.

Materia Medica for Nurses. By Emily M.A. Stoney, Head of the Training School for Nurses at Carney Hospital, South Boston, MA. 12mo volume of 300 pages. Cloth, $1.50 net.


Stoney’s Surgical Technic

Stoney’s Surgical Technique

NEW (3d) EDITION

NEW (3D) EDITION

The first part of the book is devoted to Bacteriology and Antiseptics; the second part to Surgical Technic, Signs of Death, Autopsies, Bandaging and Dressings, Obstetric Nursing, Care of Infants, etc., Hygiene and Personal Conduct of the Nurse, etc. The New York Medical Record says it “is a very practical book which presents the subjects stated in its title in a concise manner.”

The first part of the book focuses on Bacteriology and Antiseptics; the second part covers Surgical Techniques, Signs of Death, Autopsies, Bandaging and Dressings, Obstetric Nursing, Infant Care, Hygiene, and the Personal Conduct of Nurses, etc. The New York Medical Record states it “is a very practical book that presents the topics listed in its title clearly.”

Bacteriology and Surgical Technic for Nurses. By Emily M. A. Stoney. Revised by Frederic R. Griffith, M. D., New York 12mo volume of 300 pages, fully illustrated. Cloth, $1.50 net.

Bacteriology and Surgical Techniques for Nurses. By Emily Stoney. Revised by Frederic R. Griffith, M. D., New York 12mo volume of 300 pages, fully illustrated. Cloth, $1.50 net.


Aikens’ Hospital Management

Aikens' Hospital Management

JUST READY

ALL SET

This is just the work for hospital superintendents, training-school principals, physicians, and all who are actively interested in hospital administration. Each chapter has been written by one specially fitted to write upon that particular phase of the subject; and Miss Aikens has brought the various chapters into a harmonious whole.

This book is specifically for hospital superintendents, training school directors, doctors, and anyone actively involved in hospital management. Each chapter has been authored by someone uniquely qualified to discuss that specific aspect of the topic, and Miss Aikens has woven the different chapters into a cohesive whole.

Hospital Management. Arranged and edited by Charlotte A. Aikens, formerly Director of Sibley Memorial Hospital, Washington, D. C. 12mo of 488 pages, illustrated. Cloth, $3.00 net

Hospital Management. Compiled and edited by Charlotte A. Aikens, who was the Director of Sibley Memorial Hospital in Washington, D.C. 12mo of 488 pages, illustrated. Cloth, $3.00 net


Aikens’ Primary Studies for Nurses

Aikens' Essential Nursing Studies

Trained Nurse and Hospital Review says: “It is safe to say that any pupil who has mastered even the major portion of this work would be one of the best prepared first year pupils who ever stood for examination.”

Trained Nurse and Hospital Review says: “It’s safe to say that any student who has mastered even the majority of this work would be one of the best-prepared first-year students to ever take the exam.”

Primary Studies for Nurses. By Charlotte A. Aikens, formerly Director of Sibley Memorial Hospital, Washington, D. C. 12mo of 435 pages, illustrated. Cloth, $1.75 net.

Primary Studies for Nurses. By Charlotte A. Aikens, former Director of Sibley Memorial Hospital, Washington, D.C. 12mo of 435 pages, illustrated. Cloth, $1.75 net.


Aikens’ Training-School Methods and the Head Nurse

Aikens’ Training-School Methods and the Head Nurse

This work not only tells how to teach, but also what should be taught the nurse and how much. The Medical Record says: “This book is original, breezy and healthy.”

This work not only explains how to teach but also what nurses should learn and how much. The Medical Record states: “This book is fresh, engaging, and positive.”

Hospital Training-School Methods and the Head Nurse. By Charlotte A. Aikens, formerly Director of Sibley Memorial Hospital, Washington, D. C. 12mo of 267 pages. Cloth, $1.50 net.

Hospital Training-School Methods and the Head Nurse. By Charlotte A. Aikens, former Director of Sibley Memorial Hospital, Washington, D.C. 12mo of 267 pages. Cloth, $1.50 net.


Aikens’ Clinical Studies for Nurses

Aikens’ Nursing Clinical Studies

ILLUSTRATED

ILLUSTRATED

This new work is written on the same lines as the author’s successful work for primary students, taking up the studies the nurse must pursue during the second and third years.

This new work is written in the same style as the author’s successful book for primary students, covering the studies that nurses need to tackle during their second and third years.

Clinical Studies for Nurses. By Charlotte A. Aikens, formerly Director of Sibley Memorial Hospital, Washington, D. C. 12mo of 512 pages, illustrated. Cloth, $2.00 net.

Clinical Studies for Nurses. By Charlotte A. Aikens, former Director of Sibley Memorial Hospital, Washington, D.C. 12mo of 512 pages, illustrated. Cloth, $2.00 net.


Fowler’s Operating Room

Fowler’s OR

NEW (2d) EDITION

NEW (2D) EDITION

Dr. Fowler’s work contains all information of a surgical nature that a nurse must know in order to attain the highest efficiency. Canadian Journal of Medicine and Surgery says: “We find compactly and clearly stated just those thousand and one things which when required are so hard to locate.”

Dr. Fowler’s work includes all the surgical information that a nurse needs to achieve top efficiency. Canadian Journal of Medicine and Surgery states: “We find all the countless details that are so difficult to find when needed, presented in a clear and concise manner.”

The Operating Room and the Patient. By Russell S. Fowler, M. D., Professor of Surgery, Brooklyn Postgraduate Medical School. Octavo of 284 pages, with original illustrations. Cloth, $2.00 net.

The Operating Room and the Patient. By Russell S. Fowler, M. D., Professor of Surgery, Brooklyn Postgraduate Medical School. Octavo of 284 pages, with original illustrations. Cloth, $2.00 net.


Fiske’s Anatomy and Physiology

Fiske's Anatomy & Physiology

JUST READY

ALL SET

Miss Fiske weaves the physiology in with the anatomy, and in such a way that both anatomy and function are readily understood and retained by the reader.

Miss Fiske integrates physiology with anatomy in a way that makes both the structure and function easy for the reader to understand and remember.

Anatomy and Physiology for Nurses. By Annette Fiske. A. M., Graduate of the Waltham Training School for Nurses, Massachusetts. 12mo of 250 pages, illustrated.

Anatomy and Physiology for Nurses. By Annette Fiske. A. M., Graduate of the Waltham Training School for Nurses, Massachusetts. 12mo of 250 pages, illustrated.


Beck’s Reference Handbook

Beck's Guidebook

NEW (2d) EDITION

NEW (2D) EDITION

This book contains all the information that a nurse requires to carry out any directions given by the physician. The Montreal Medical Journal says it is “cleverly systematized and shows close observation of the sickroom and hospital regime.”

This book has all the information that a nurse needs to follow any instructions from the physician. The Montreal Medical Journal describes it as “well organized and demonstrates careful observation of the sickroom and hospital routine.”

A Reference Handbook for Nurses. By Amanda K. Beck, Graduate of the Illinois Training School for Nurses, Chicago, Ill. 32mo volume of 200 pages. Bound in flexible leather, $1.25 net.

A Reference Handbook for Nurses. By Amanda K. Beck, Graduate of the Illinois Training School for Nurses, Chicago, IL. 32mo volume of 200 pages. Bound in flexible leather, $1.25 net.


Boyd’s State Registration for Nurses

Boyd's Nurse State Registration

This book tells the nurse just what she must know in order to obtain a certificate in any State. It presents comparative summaries of the laws, requirements, fees, exceptions and restrictions, violations and their penalties. The work will also form a serviceable basis for the drafting of laws.

This book tells nurses exactly what they need to know to get certified in any state. It provides comparative summaries of the laws, requirements, fees, exceptions and restrictions, violations, and their penalties. The work will also serve as a useful foundation for drafting laws.

State Registration for Nurses. By Louie Croft Boyd, R. N., Graduate Colorado Training School for Nurses. Price, 50 cents net.

State Registration for Nurses. By Louie Croft Boyd, R. N., Graduate of Colorado Training School for Nurses. Price, 50 cents net.


DeLee’s Obstetrics for Nurses

DeLee’s Obstetrics for Nurses

THIRD EDITION

3rd Edition

Dr. DeLee’s book really considers two subjects—obstetrics for nurses and actual obstetric nursing. Trained Nurse and Hospital Review says the “book abounds with practical suggestions, and they are given with such clearness that they cannot fail to leave their impress.”

Dr. DeLee’s book really focuses on two topics—nursing in obstetrics and practical obstetric nursing. Trained Nurse and Hospital Review states that the “book is full of useful suggestions, and they are presented so clearly that they are sure to make an impact.”

Obstetrics for Nurses. By Joseph B. DeLee, M. D., Professor of Obstetrics at the Northwestern University Medical School, Chicago. 12mo volume of 512 pages, fully illustrated. Cloth, $2.50 net.

Obstetrics for Nurses. By Joseph B. DeLee, M. D., Professor of Obstetrics at the Northwestern University Medical School, Chicago. 12mo volume of 512 pages, fully illustrated. Cloth, $2.50 net.


Davis’ Obstetric & Gynecologic Nursing

Davis’ OB & GYN Nursing

THE NEW (3d) EDITION

THE NEW (3D) EDITION

The Trained Nurse and Hospital Review says: “This is one of the most practical and useful books ever presented to the nursing profession.” The text is illustrated.

The Trained Nurse and Hospital Review says: “This is one of the most practical and useful books ever presented to the nursing profession.” The text is illustrated.

Obstetric and Gynecologic Nursing. By Edward P. Davis, M. D., Professor of Obstetrics in the Jefferson Medical College, Philadelphia. 12mo volume of 436 pages, illustrated. Buckram, $1.75 net.

Obstetric and Gynecologic Nursing. By Edward P. Davis, M.D., Professor of Obstetrics at Jefferson Medical College, Philadelphia. 12mo volume with 436 pages, illustrated. Buckram, $1.75 net.


Macfarlane’s Gynecology for Nurses

Macfarlane’s Gynecology for Nurses

ILLUSTRATED

ILLUSTRATED

Dr. A. M. Seabrook, Woman’s Hospital of Philadelphia, says: “It is a most admirable little book, covering in a concise but attractive way the subject from the nurse’s standpoint. You certainly keep up to date in all these matters, and are to be complimented upon your progress and enterprise.”

Dr. A. M. Seabrook, Woman’s Hospital of Philadelphia, says: “This is a fantastic little book that presents the topic clearly and engagingly from the nurse's perspective. You definitely stay current in all these areas, and you should be praised for your progress and initiative.”

A Reference Handbook of Gynecology for Nurses. By Catharine MacFarlane, M. D., Gynecologist to the Woman’s Hospital of Philadelphia. 32mo of 150 pages, with 70 illustrations. Flexible leather, $1.25 net.

A Reference Handbook of Gynecology for Nurses. By Catharine MacFarlane, M.D., Gynecologist to the Woman’s Hospital of Philadelphia. 32mo of 150 pages, with 70 illustrations. Flexible leather, $1.25 net.


McKenzie’s Exercise in Education and Medicine

McKenzie’s Approach to Education and Medicine

Exercise in Education and Medicine. By R. Tait McKenzie, B. A., M. D., Professor of Physical Education, and Director of the Department, University of Pennsylvania. Octavo of 406 pages, with 346 illustrations. Cloth, $3.50 net.

Exercise in Education and Medicine. By R. Tait McKenzie, B. A., M. D., Professor of Physical Education, and Director of the Department, University of Pennsylvania. Octavo of 406 pages, with 346 illustrations. Cloth, $3.50 net.


Manhattan Hospital Eye, Ear, Nose, and Throat Nursing

Manhattan Hospital Eye, Ear, Nose, and Throat Nursing

ILLUSTRATED

ILLUSTRATED

This is a practical book, prepared by surgeons who, from their experience in the operating amphitheatre and at the bedside, have realized the shortcomings of present nursing books in regard to eye, ear, nose, and throat nursing.

This is a practical book created by surgeons who, from their experience in the operating room and at the bedside, have noticed the limitations of current nursing books when it comes to eye, ear, nose, and throat care.

Nursing in Diseases of the Eye, Ear, Nose and Throat. By the Committee on Nurses of the Manhattan Eye, Ear, and Throat Hospital: J. Edward Giles, M. D., Surgeon in Eye Department; Arthur B. Duel, M. D., (chairman), Surgeon in Ear Department; Harmon Smith, M. D., Surgeon in Throat Department. Assisted by John R. Shannon, M. D., Assistant Surgeon in Eye Department; and John R. Page, M. D., Assistant Surgeon in Ear Department. With chapters by Herbert B. Wilcox, M. D., Attending Physician to the Hospital; and Miss Eugenia D. Ayers, Superintendent of Nurses. 12mo of 260 pages, illustrated. Cloth, $1.50 net.

Nursing in Diseases of the Eye, Ear, Nose, and Throat. By the Committee on Nurses of the Manhattan Eye, Ear, and Throat Hospital: J. Edward Giles, M. D., Surgeon in the Eye Department; Arthur B. Duel, M. D., (chairman), Surgeon in the Ear Department; Harmon Smith, M. D., Surgeon in the Throat Department. Assisted by John R. Shannon, M. D., Assistant Surgeon in the Eye Department; and John R. Page, M. D., Assistant Surgeon in the Ear Department. With chapters by Herbert B. Wilcox, M. D., Attending Physician to the Hospital; and Miss Eugenia D. Ayers, Superintendent of Nurses. 12mo of 260 pages, illustrated. Cloth, $1.50 net.


Friedenwald and Ruhrah’s Dietetics for Nurses

Friedenwald and Ruhrah’s Dietetics for Nurses

NEW (2d) EDITION

NEW (2D) EDITION

This work has been prepared to meet the needs of the nurse, both in training school and after graduation. American Journal of Nursing says it “is exactly the book for which nurses and others have long and vainly sought.”

This work has been created to address the needs of nurses, both in training programs and after graduation. American Journal of Nursing states it “is exactly the book that nurses and others have long and unsuccessfully searched for.”

Dietetics for Nurses. By Julius Friedenwald, M. D., Professor of Diseases of the Stomach, and John Ruhrah, M. D., Professor of Diseases of Children, College of Physicians and Surgeons, Baltimore. 12mo volume of 395 pages. Cloth, $1.50 net

Dietetics for Nurses. By Julius Friedenwald, M.D., Professor of Stomach Diseases, and John Ruhrah, M.D., Professor of Pediatric Diseases, College of Physicians and Surgeons, Baltimore. 12mo volume of 395 pages. Cloth, $1.50 net


Friedenwald & Ruhrah on Diet

Friedenwald & Ruhrah on Diet

THIRD EDITION

3rd Edition

Diet in Health and Disease. By Julius Friedenwald, M. D., and John Ruhrah, M. D. Octavo volume of 764 pages. Cloth, $4.00 net.

Diet in Health and Disease. By Julius Friedenwald, M. D., and John Ruhrah, M. D. Octavo volume of 764 pages. Cloth, $4.00 net.


Galbraith’s Personal Hygiene and Physical Training for Women

Galbraith’s Personal Hygiene and Physical Training for Women

JUST ISSUED

JUST ISSUED

Personal Hygiene and Physical Training for Women. By Anna M. Galbraith, M. D., Fellow New York Academy of Medicine. 12mo of 371 pages, illustrated. Cloth, $2.00 net.

Personal Hygiene and Physical Training for Women. By Anna M. Galbraith, M. D., Fellow New York Academy of Medicine. 12mo of 371 pages, illustrated. Cloth, $2.00 net.


Galbraith’s Four Epochs of Woman’s Life

Galbraith’s Four Stages of a Woman’s Life

THE NEW (2d) EDITION

THE NEW (2nd) EDITION

The Four Epochs of Woman’s Life. By Anna M. Galbraith, M. D. With an Introductory Note by John H. Musser, M. D., University of Pennsylvania. 12mo of 247 pages. Cloth, $1.50 net.

The Four Epochs of Woman’s Life. By Anna M. Galbraith, M. D. With an Introductory Note by John H. Musser, M. D., University of Pennsylvania. 12mo of 247 pages. Cloth, $1.50 net.


McCombs’ Diseases of Children for Nurses

McCombs' Diseases of Children for Nurses

JUST ISSUED—NEW (2d) EDITION

JUST ISSUED—NEW (2nd) EDITION

Dr. McCombs’ experience in lecturing to nurses has enabled him to emphasize just those points that nurses most need to know. National Hospital Record says: “We have needed a good book on children’s diseases and this volume admirably fills the want.” The nurse’s side has been written by head nurses, very valuable being the work of Miss Jennie Manly.

Dr. McCombs' experience in teaching nurses has allowed him to highlight exactly the points that nurses really need to understand. National Hospital Record states: “We have needed a solid book on children's diseases, and this volume perfectly meets that need.” The section for nurses has been written by head nurses, with Miss Jennie Manly's contributions being particularly valuable.

Diseases of Children for Nurses. By Robert S. McCombs, M. D., Instructor of Nurses at the Children’s Hospital of Philadelphia. 12mo of 470 pages, illustrated. Cloth, $2.00 net

Diseases of Children for Nurses. By Robert S. McCombs, M. D., Instructor of Nurses at the Children’s Hospital of Philadelphia. 12mo of 470 pages, illustrated. Cloth, $2.00 net


Wilson’s Obstetric Nursing

Wilson's Maternity Nursing

In Dr. Wilson’s work the entire subject is covered from the beginning of pregnancy, its course, signs, labor, its actual accomplishment, the puerperium and care of the infant. American Journal of Obstetrics says: “Every page emphasizes the nurse’s relation to the case.”

In Dr. Wilson’s work, the whole topic is discussed from the start of pregnancy, its progress, signs, labor, the actual delivery process, the postpartum period, and the care of the baby. American Journal of Obstetrics states: “Every page highlights the nurse’s role in the case.”

A Reference Handbook of Obstetric Nursing. By W. Reynolds Wilson, M. D., Visiting Physician to the Philadelphia Lying-in Charity. 32mo of 355 pages, illustrated. Flexible leather, $1.25 net.

A Reference Handbook of Obstetric Nursing. By W. Reynolds Wilson, M.D., Visiting Physician to the Philadelphia Lying-in Charity. 32mo of 355 pages, illustrated. Flexible leather, $1.25 net.


American Pocket Dictionary

American Pocket Dictionary

NEW (6th) EDITION

NEW (6th) EDITION

The Trained Nurse and Hospital Review says: “We have had many occasions to refer to this dictionary, and in every instance we have found the desired information.”

The Trained Nurse and Hospital Review says: “We've often needed to reference this dictionary, and every time, we've found the information we were looking for.”

American Pocket Medical Dictionary. Edited by W. A. Newman Dorland, A. M., M. D., Loyola University, Chicago. Flexible leather, gold edges, $1.00 net; with patent thumb index, $1.25 net.

American Pocket Medical Dictionary. Edited by W. A. Newman Dorland, A. M., M. D., Loyola University, Chicago. Flexible leather, gold edges, $1.00; with patent thumb index, $1.25.


Lewis’ Anatomy and Physiology

Lewis' Anatomy and Physiology

SECOND EDITION

2nd Edition

Nurses Journal of Pacific Coast says “it is not in any sense rudimentary, but comprehensive in its treatment of the subjects.” The low price makes this book particularly attractive.

Nurses Journal of Pacific Coast says “it's not basic at all, but thorough in how it covers the topics.” The affordable price makes this book especially appealing.

Anatomy and Physiology for Nurses. By LeRoy Lewis, M. D., Lecturer on Anatomy and Physiology for Nurses, Lewis Hospital, Bay City, Mich. 12mo of 375 pages, 150 illustrations. Cloth, $1.75 net.

Anatomy and Physiology for Nurses. By LeRoy Lewis, M.D., Instructor in Anatomy and Physiology for Nurses, Lewis Hospital, Bay City, Michigan. 12mo of 375 pages, 150 illustrations. Cloth, $1.75 net.


Dorland’s Illustrated Dictionary

Dorland's Illustrated Dictionary

NEW (5th) EDITION

NEW (5TH) EDITION

The American Illustrated Medical Dictionary. Edited by W. A. N. Dorland, M. D. Large octavo of 876 pages, 293 illustrations, 119 in colors. Flexible leather, $4.50 net; thumb indexed, $5.00 net.

The American Illustrated Medical Dictionary. Edited by W. A. N. Dorland, M. D. Large octavo with 876 pages, 293 illustrations, 119 in color. Flexible leather, $4.50 net; thumb indexed, $5.00 net.


Paul’s Materia Medica

Paul's Medical Handbook

A Text-Book of Materia Medica for Nurses. By George P. Paul, M. D., Samaritan Hospital, Troy, N. Y. 12mo of 240 pages. Cloth, $1.50 net.

A Text-Book of Materia Medica for Nurses. By George P. Paul, M. D., Samaritan Hospital, Troy, NY. 12mo of 240 pages. Cloth, $1.50 net.


Paul’s Fever Nursing

Paul's Fever Care

Nursing in the Acute Infectious Fevers. By George P. Paul, M. D. Cloth, $1.00 net.

Nursing in the Acute Infectious Fevers. By George P. Paul, M. D. Cloth, $1.00 net.


Hoxie’s Medicine for Nurses

Hoxie’s Guide for Nurses

Practice of Medicine for Nurses. By George Howard Hoxie, M. D., University of Kansas. With a chapter on Technic of Nursing by Pearl L. Laptad. 12mo of 284 pages, illustrated. Cloth, $1.50 net.

Practice of Medicine for Nurses. By George H. Hoxie, M. D., University of Kansas. Includes a chapter on Nursing Techniques by Pearl L. Laptad. 12mo of 284 pages, illustrated. Cloth, $1.50 net.


Grafstrom’s Mechano-therapy

Grafstrom’s Mechano-Therapy

SECOND EDITION

2nd Edition

Mechano-therapy (Massage and Medical Gymnastics). By Axel V. Grafstrom, B. Sc., M. D., 12mo, 200 pages. Cloth, $1.25 net.

Mechano-therapy (Massage and Medical Gymnastics). By Axel V. Grafstrom, B. Sc., M. D., 12mo, 200 pages. Cloth, $1.25 net.


Nancrede’s Anatomy

Nancrede’s Anatomy

NEW (7th) EDITION

NEW (7th) EDITION

Essentials of Anatomy. Charles B. G. DeNancrede, M. D., University of Michigan. 12mo, 400 pages, 180 illustrations. Cloth, $1.00 net.

Essentials of Anatomy. Charles B. G. DeNancrede, M. D., University of Michigan. 12mo, 400 pages, 180 illustrations. Cloth, $1.00 net.


Morrow’s Immediate Care of Injured

Morrow’s Immediate Care for Injured

Immediate Care of the Injured. By Albert S. Morrow, M. D., New York City Home for Aged and Infirm. Octavo of 340 pages, with 238 illustrations. Cloth, $2.50 net.

Immediate Care of the Injured. By Albert S. Morrow, M. D., New York City Home for Aged and Infirm. Octavo of 340 pages, with 238 illustrations. Cloth, $2.50 net.


Register’s Fever Nursing

Register’s Fever Care

A Text-Book on Practical Fever Nursing. By Edward C. Register, M. D., North Carolina Medical College. Octavo of 350 pages, illustrated. Cloth, $2.50 net.

A Text-Book on Practical Fever Nursing. By Edward C. Register, M. D., North Carolina Medical College. Octavo of 350 pages, illustrated. Cloth, $2.50 net.


Pyle’s Personal Hygiene

Pyle's Personal Care

NEW (4th) EDITION

NEW (4th) EDITION

A Manual of Personal Hygiene. Edited by Walter L. Pyle, M. D. Wills Eye Hospital, Philadelphia. 12mo, 472 pages, illus. $1.50 net.

A Manual of Personal Hygiene. Edited by Walter L. Pyle, M. D. Wills Eye Hospital, Philadelphia. 12mo, 472 pages, illustrations. $1.50 net.


Morris’ Materia Medica

Morris' Medical Reference

NEW (7th) EDITION

NEW (7th) EDITION

Essentials of Materia Medica, Therapeutics, and Prescription Writing. By Henry Morris, M. D. Revised by W. A. Bastedo, M. D., Columbia University, N. Y. 12mo of 300 pages, illustrated. Cloth, $1.00 net.

Essentials of Materia Medica, Therapeutics, and Prescription Writing. By Henry Morris, M. D. Revised by W.A. Bastedo, M. D., Columbia University, N. Y. 12mo of 300 pages, illustrated. Cloth, $1.00 net.


Griffith’s Care of the Baby

Griffith's Baby Care

JUST ISSUED NEW (5th) EDITION

JUST ISSUED 5th EDITION

The Care of the Baby. By J. P. Crozer Griffith, M. D., University of Pennsylvania. 12mo of 455 pages, illustrated. Cloth, $1.50 net.

The Care of the Baby. By J.P. Crozer Griffith, M. D., University of Pennsylvania. 12mo of 455 pages, illustrated. Cloth, $1.50 net.


Transcriber’s Notes:

Transcriber's Notes:


The cover image was created by the transcriber, and is in the public domain.

The cover image was made by the transcriber and is in the public domain.

The illustrations have been moved so that they do not break up paragraphs and so that they are next to the text they illustrate.

The illustrations have been repositioned so they don't disrupt the paragraphs and are placed next to the text they depict.

Typographical and punctuation errors have been silently corrected.

Typographical and punctuation errors have been quietly fixed.


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