THE MWROSCOQT‘C WTGfifiY 0F THE SKfiN ANfi EXTERNAL EAR CF FEMS DOMESTiC‘JS TM: for m Dogm cf M. S. MCHSGAN- STATE UNEV’ERSETY 35mm H. Sh‘écklmd 1958 .A‘ :43 . irativ THE MICROSCOPIC ANATOMY OF THE SKIN AND EXTERNAL EAR OF FELIS DOMESTICUS by James H. Strickland A THESIS Submitted to the College of Veterinary Medicine Michigan State University of Agriculture and Applied Science in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Department of Anatomy 1958 ) ACKNOWLEDGMENTS With sincerity and deep appreciation, the writer wishes to thank Dr. M. Lois Calhoun, Professor and Head of the Department of Anatomy, for her untiring and under- standing assistance in planning and guiding this problem. The writer is also grateful to Dr. Esther M. Smith for her very helpful assistance in photography, and other members of the Anatomy Department for their suggestions and assistance. He also wishes to express his appreciation to Leo w. Walker, M. D., and staff of the clinical path- ology laboratory of St. Lawrence Hospital for their unusual cooperation. The writer is deeply indebted to the Depart- ment of Surgery and Medicine for procuring normal animals used in this investigation. TABLE OF CONTENTS INTRODUCTION. . . . . . . REVIEW OF LITERATURE Epidermis. Dermis. Hair follicle Sebaceous glands Sweat glands. MATERIAL AND METHODS RESUITS AND DISCUSSION General. Specific epidermal layers. Stratum corneum. Stratum lucidum. Stratum granulosum. Stratum spinosum Stratum cylindricum Pigment. Dermis . . . . . . . Hairy skin area. Areas with little or no hair External auditory meatus. Metacarpal pad PAGE CDWU'l-P‘JEUJTD 14 14 .18 .18 .19 .19 .19 .2O .2O .21 .21 .22 .23 .23 Planum nasale. Lip Special skin areas Hair Follicular folds. Tactile hairs. Mm. arrectores pilorum. Sebaceous glands Hairy skin areas. Areas with little or no hair. Metacarpal pad External auditory meatus Upper and lower lip. Special skin areas Supracaudal organ Upper and lower eyelids Prepuce. Teat. Scrotum. Sweat glands Saccular apocrine Coiled apocrine Coiled merocrine. Ceruminous glands. Special body areas . . . PAGE Teat. . . . . . . . . . . . . . 3A Prepuce. . . . . . . . . . . . . 35 Scrotum. . . . . . .. . . . . . . 35 Anal sac and associated glands . . . . . 35 Ear pinna . . . . . . . . . . . . 35 SUMMARY AND CONCLUSIONS. . . . . . . . . . . 37 LITERATURE CITED . . . . . . . . . . . . . 87 FIGURE A. B. LIST OF FIGURES Body areas from which tissues were taken. Ear areas from which tissues were taken LIST OF TABLES TABLE PAGE I. The measurement of epidermal and dermal thickness in the hairy skin areas. . . . . . . . . 15 II. The hair group density in the hairy skin from oblique sections . . . . . . . . . . . 16 III. Size of mm. arrectores pilorum at the base of attachment . . . . . . . . . . . . . 28 PLATE 'f' a} c. C III. >4 r~t >< T't rm ><‘. #4 k4 r i >4 4 2 H r1 i—-1 t-i I-i >4 H >4 LIST OF PLATES Integumentary papilla in the hairy skin. An abnormal external auditory meatus. Dense hairy skin area showing the hair groups. The dorsal lumbar portion of the hairy skin The metacarpal pad. Tubercle in anthelix from outer third of the external auditory meatus The lower third of a normal external auditory meatus The metacarpal pad showing distribution of elastic tissue The nose print area of the planum nasale Special nerve ending in lip Subcutis of the foot pad. Supracaudal gland area Guard hairs showing the follicular folds Lip-oblique A branching arrector pili muscle Lip-longitudinal Upper eyelid. Sweat glands of the scrotum. Tactile hairs \N 0\ U1 OO O\ ‘J 0\ ID a. 66 68 73 PLATE XX. XXI. Small sweat gland emptying into the upper portion of a hair follicle. Anal sac and associated glands ix PAGE 8A 86 INTRODUCTION This investigation resulted from a lack of sufficient information on the normal histology of cat skin and a request from the department of Surgery and Medicine for reliable data on the histology of the external auditory meatus of the cat. The field of dermatopathology relies on knowledge of the normal, and with the various patho- logical involvements of the skin and external ear canal of cats, it is hoped that this work will serve as a reference. GENERAL REVIEW OF LITERATURE Relatively little work has been done on the histology of cat skin. According to Speed (19A1), Backmund (1904) worked on the embryology of the sweat glands in the cat, and Teger (1906) reported active sweat glands in the exter- nal auditory meatus. Stoss (1906) was one of the first to discuss the histology of cat skin. Frei (1928) studied the histology of the cat foot pad, while Thuringer (1939) studied the epidermal mitotic index of this same area. Trimarchi (1929) reported on the sebaceous and sudoriferous glands in the nasal vestibule of domestic carnivores. Varidak (1941) devoted part of his study of domestic animal skin to that of the cat. Montagna (1949) described the glands in the external auditory canal, and in 1952 reported on the epidermis. Tekada (1951) also studied the skin of the external auditory canal of the cat and other domestic animals, and Senturia and Liebmann (1956) studied the factors which may contribute to external ear infections of the cat. Trautmann and Fiebiger (1957) gave a detailed description of carnivore skin including some specific infor- mation on the cat. Daniel and Prichard (1956) described the arteriovenous anastomoses in the cat and eight other animals. They found an S shaped anastomosis less complex and smaller than in most animals studied. Kuntz and 2 Hamilton (1938) found afferent fibers associated with smaller blood vessels, lamellated end organs in the fore- limb and foot pad, and a subepidermal plexus made up of slender nerve strands. Winkelmann (1957) described the sensory end organ of the hairless skin of the cat. Trautmann and Fiebiger (1957) found Pacinian corpuscles in the prepuce of the cat. Kamamura (1957) reported the cytochemical effect of pilocarpine administration on cat sweat glands, and described two different types of cells, a superficial and a basal cell composing the secretory unit of the plantar foot pad. Dukes (1955) and Marzulli and Callahan (1957) studied the sweat capacity of the cat. Epidermis Frei (1928) found that the foot pads of the cat have a thick epidermis with a superficial horny layer. Wavy lines separate the cornified cells in the stratun corneum and the epidermis is pierced by excretory ducts. According ' do not to Frei ”foot pads that possess functional glands,‘ have typically arranged cornified cells. Stoss (1906) reported six epidermal strata in the external border of the nasal septum of the cat. Thuringer (1939) found 2.37 dividing cells per thousand in the cat foot pad. Varidak (1941) observed that the epidermis of the cat resembles that of man, but the superficial translucent layer seldom occurs, while the stratum lucidum is usually present. Montagna (1952) noted all epidermal layers in the cat digital pads. Dermis Stoss (1936) observed dense, tough connective tissue fibers in the cat dermis. Frei (1928) reported that the foot pads of the cat are similar to those of the dog, and are composed of four rounded pads. The thumb pad is the weakest, and is absent from the hind feet. He found closely arranged extremely vascular, short papillae, a less devel- oped stratum reticulare, and a well developed subcutis. Trautmann and Fiebiger (1957) described thick layers of fat in the foot pads of carnivores. Hair Follicle Trautmann and Fiebiger (1957) found bundles of hair projecting from common follicular openings in carnivores. According to these authors three cover hairs composed of one larger main hair and two smaller hairs usually consti- tute a group and in the carnivore each group is surrounded by six to twelve lanugo or wool hairs. Stoss (1936) and Trautmann and Fiebiger (1957) described nontrabecular annular sinuses associated with the large tactile hairs of the cat. These sinuses are smooth walled with a cushion- like thickening. \fl Sebaceous Glands Trautmann and Fiebiger (1957) found sebaceous glands in all body areas of carnivores except the foot pads and planum nasale. They reported a ring of sebaceous glands opening into the tactile hair follices and large sebaceous glands, "the supracaudal organ," on the dorsal surface of the cat tail. Stoss (1936) reported many sebaceous glands on the back, chest, and abdomen of the cat, and found two to three lobulated sebaceous glands emptying into a single hair follicle. He also observed large sebaceous glands in the upper Jaw, prepuce, and proximal dorsal end of the cat tail, but generally small glands were present in other body areas. Trautmann and Fiebiger (1957) reported sebaceous glands independent of hair follicles in the pre— puce, external auditory meatus, and tarsal glands of the eye lids in domestic animals. Montagna (1949) described large clusters of sebaceous glands in the external auditory meatus and stated that these may or may not be associated with lanugo hair follicles. He also reported that sebaceous glands exhibit considerable mitoses particularly at the periphery of the acini, and contain a moderate amount of stored lipoids. Trautmann and Fiebiger (1957) observed sebaceous glands in the teat of the Cat, mare, and bitch. Sweat Glands Frei (1928) found sweat glands in the foot pads of carnivores, and Dukes (1955) stated that active sweat 6 glands are confined to the foot pads in the cat, dog, pig, and ox. Trautmann and Fiebiger (1957) stated that the prepuce of domestic animals contains prominent tubular glands. According to these authors well developed sebaceous and tubular skin glands are found in the scrotal skin of all domestic animals except the boar, in which they are scarce and small. Marzulli and Callahan (1957) in testing the capacity of certain laboratory animals to sweat observed that the cat did not sweat in hairy skin areas. They observed an apocrine type of active tubular sweat gland only in the foot pads of the cat, dog, and rat and in the palms of the monkey. Stoss (1906) found that sweat glands are well developed on the lips, plantar pad, ball of the toe and anus of the cat, but are difficult to demonstrate in the remaining areas. According to Habel (1958), Ellenberger and associates reported sweat glands in almost all skin areas, even extending to the level of the papillae of cover hairs. Stoss (1906) found that the sweat glands reach as far as the root of the hair follicle, and that the secretory ducts are narrow and undulating making up one-third of the total length of the ducts. Trautmann and Fiebiger (1957) described coiled secretory tubules in the cat, and Stoss (1906) reported a tapered excretory duct opening into the hair follicle and onto the surface of the foot pad. Stoss concluded that all hair follicles have adjacent sweat glands which empty into their respective follicle, while lanugo hairs possess no such glands. According to Speed (1941),Backmund (1904) concluded that the sweat glands of the upper and lower Jaw have a special shape and that fetal hair has a sweat gland but no free openings. Trautmann and Fiebiger (1957) described apocrine and sebaceous glands in the anal sac of the cat and tubular and alveolar glands in the excretory duct of the anal sac. According to Speed (1941), Teger (1936) observed active sweat glands in the external auditory meatus of the cat. Montagna (1949) working on the cat found both coiled dilated tubular sudoriparous glands and sebaceous glands opening either into the upper portion of the hair follicle or directly onto the surface of the external auditory meatus. MATERIAL AND METHODS A total of twenty domestic cats including eight mature animals, five females and three noncastrated males, one incomplete immature female, and one immature male were used for this study. Supplemental sections were secured from ten other cats. The animals were obtained from the departments of Physiology and Pharmacology, Surgery and Medicine, and Anatomy and were sacrificed with a lethal dose of sodium pentothal. Sections approximately one-half inch square were taken from twenty-seven body areas as indicated in Figures A and B. Since Frei (1928) found all the foot pads to be similar, the metacarpal pad was taken as a representative example. The tissues were fixed in formalin-alchol-acetic acid (Lavdowsky‘s mixture, Guyer- 1949), and embedded in'"Tissuemat,fl'according to the methods of Johnson §£.§l° (1943). Longitudinal and frontal sections werepueparedvfiifl1a.modified hematoxylin and eosin (Malewitz and Smith 1955), Weigerts and Van Gieson's connective tissue stain, Wright's blood stain for mast cells (Belanger gt §l° 1957), and Yang's (1952) method for pigment determination. Measurements of skin thickness were made in ten represen— tative body areas. The epidermis was measured in microns l"Tissuemat"--F3sher Scientific Company, Pittsburgh, Pennsylvania. 8 and sketched on graph paper by projection for future reference and general comparison. The units of graph paper were given values according to the calibration of the microscope. The dermis was measured in four respective fields at the highest and lowest points. The averages are given in Table I. \n \OCD\10\ 11. 12. BODY APEAS FROM WHICH TISSUES Supraorbital region Upper eyelid Lower eyelid Planum nasale Upper lip Lower lip Dorsal neck Thoracicolumbar region Lateral body wall Ventral abdomen 13. 21. 22A. 223. WER TAKEN Tail root Shoulder Lateral foreleg Lateral thigh Lateral hindleg Scrotum Supracaudal gland Teat (female) Prepuce Anal sac Metacarpal pad ll noxme who; moSmmHB noagz EOAM mmop< zoom .< mpswfim .wa 34. 11.1.9: 5 3 12 23-1. 23-2. 24-1. 24-2. 25. 26. 27-1. 27-2. Figure B EAR AREAS FROM WHICH TISSUES WERE TAKEN Apex of pinna Scapha of pinna Auditory longitudinal meatus--medial wall Auditory longitudinal meatus-~lateral wall Upper one-third of meatus-~level 1 Upper one-third of meatus--level 2 Middle meatus--leve1 1 Lower section near tympanic membrane--level 2 Lower middle meatus--1evel 2 Lower one-third of meatus-~level l Figure B. Anterolateral view of cat's ear \OOO'\10\\N 4:me Cut edge of tragus Rostral border Caudal border Anthelix (tubercle of) Posterior auricular sulcus Antitragus Anterior auricular sulcus Plica antitragica Incisure intertragica Scapha Longitudinal ear folds Transverse folds 1.53 'H'BJ Figure B. Anterolateral view of cat's ear 1. Cut edge of tragus 2. Rostral border 3. Caudal border 4. Anthelix (tubercle of) 5. ~Posterior auricular sulcus 6. Antitragus 7. Anterior auricular sulcus 8. Plica antitragica 9. Incisure intertragica 10. Scapha ll. Longitudinal ear folds l2. Transverse folds 13 RESULTS AND DISCUSSION I. GENERAL From a comparative viewpoint most investigators have assumed the skin of the cat to be similar to the skin of the dog. This is essentially true but certain apparent differences will be pointed out in the following discussion. Due to certain area limitations and specialization, the ten general body regions shown in Table I were selected as most typical for an over-all picture. The thickest areas are found on the dorsal neck, lumban and sacral regions. The thinnest areas are on the lateral sides of the lower hind leg, thigh, and lower fore- leg. Generally the thickness decreases from dorsal to ventral on the trunk, and from proximal to distal on both front and hind limbs. The maximum skin thickness is 1905 microns in the dorsal neck region and a minimum of 374 microns on the lower lateral side of the hind leg. The epidermis is thin in all hairy areas, usually measuring between twenty and thirty microns, with a range from twelve to forty-five microns. According to Lovell and Getty (1957), the average epidermal thickness in the hairy skin of mongrel dogs is thirty to forty microns. Webb and Calhoun (1954) reported the thinnest epidermis in 14 ‘A'llll'l'I It'll II" I 'I‘ 15 mongrel dogs to be 26.5 microns in the sternal region. In the present investigation twenty-five microns is con- sidered an average epidermal thickness in the cat. One may assume that the epidermis in mongrel dogs is generally thicker than that of the cat in the hairy skin areas. The epidermis of the prepuce, scrotum, and similar specialized. areas of the cat ranged from seventeen to sixty microns, while similar areas in mongrel dogs measured sixty-seven to ninety microns (Webb and Calhoun 1954). Small hairless knoblike enlargements in the hairy skin area of mongrel dogs have been referred to as epidermal papillae by Lovell and Getty (1957). Since both the dermis and epidermis are involved in this structure the term integumentary papillae seems more appropriate (Plate I). The epidermis of these integumentary papillae in the cat is thicker than the epidermis of most hairy areas. Occasional epidermal thickness to 100 microns may be seen in the anal sac lumen. The thickest epidermis is found in the digital pads and planum nasale and measures 900 microns compared to 1,800 microns seen in mongrel dogs (Lovell and Getty 1957). 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