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Skin biopsy specimens of normal llama skin were examined histologically. Adnexal structures similar to those of most other domestic mammals included epitrichial sweat glands, sebaceous glands and arrector pili muscles. Unique features of normal llama skin included a very thick dermis with marked differences between superficial and deep dermis, prominent cutaneous vascular plexuses, unidentified cells with eosinophilic granules within the adventitia of the vascular plexuses, both simple and compound hair follicles, ‘metatarsal glands’, ‘interdigital glands’, footpad glands and the absence of eyelid tarsal glands.

An 11-year-old Doberman Pinscher with clinical and histological skin features consistent with colour dilution alopecia had a long history of skin disease. The animal had hundreds of papules affecting the ‘blue’ haired areas of the hair coat. The predominant skin lesions included keratinizing infundibular cysts, keratin horns, perifollicular dermatitis, and sebaceous hyperplasia; these lesions were often accompanied by furunculosis and suppurative panniculitis. Over a 9-month period, 32 lesions were examined histologically, which included two lipomas, one infiltrative lipoma, one squamous papilloma, two mast cell tumours, four cavernous haemangiomas, one haemangiosarcoma, and three melanomas. It is unknown at present whether the colour dilution phenotype confers increased risk for tumours of the skin and or subcutaneous tissues. Resume— Un doberman de 11 ans avec des manifestations cutanees cliniques et histologiques compatibles avec le diagnostic d'alopecie des couleurs diluees avait une longue histoire de problemes cutanes. L'animal presentait des centaines de papules affectant les zones de couleur bleue. Les lesions cutanees predominantes consistaient en kystes infundibulaires keratinisants, cornes cutanees, dermatite perifolliculaire et hyperplasie sebacee; ces lesions s'accompagnaient souvent de furonculose et de panniculite suppurative. Sur une periode de 9 mois, 32 lesions ont fait l'objet d'un examen histologique, dont deux lipomes, un lipome infiltrant, un papillome, deux mastocytomes, quatre hemangiomes caverneux, un hemangiosarcome, et trois melanomes. On ne sait actuellement pas si le phenotype couleur diluee constitue un facteur de risque accru pour les tumeurs de la peau et des tissus sous cutanes. [Madewell, B. R., Ihrke, P. J., Griffey, S. M. Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia. (Tumeurs cutanees multiples chez un doberman presentant une alopecie des couleurs diluees.) Veterinary Dermatology 1997; 8: 59–62.] Resumen Un doberman pinscher de 11 anos con caracteristicas clinicas e histologicas compatibles con alopecia de color diluido tenia una larga historia de enfermedad cutanea. El animal presentaba centenares de papulas afectando las areas de pelo “azul”. Las lesiones predominantes incluian quistes infundibulares queratinizados, cuernos de queratina, dermatitis perifolicular e hiperplasia sebacea; estas lesiones se acompanaban de furunculosis y paniculitis supurativa. Durante un periodo de 9 meses, 32 lesiones fueron examinadas histologicamente, incluyendo 2 lipomas, un lipoma infiltrativo, un papiloma escamoso, dos mastocitomas, cuatro hemangiomas cavernosos, un hemangiosarcoma y tres melanomas. Se desconoce aun si el fenotipo de color diluido aumenta el riesgo para la aparicion de tumores en tejidos cutaneos y subcutaneos. [Madewell, B. R., Ihrke, P. J., Griffey, S. M. Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia. (Multiples tumores cutaneos en un Doberman Pinscher con alopecia de color diluido.) Veterinary Dermatology 1997; 8: 59–62.] Zusammenfassung— Ein elfjahriger Dobermann mit klinischen und histologischen Befunden, die bei Farbmutantenalopezie auftreten, wies eine lange Vorgeschichte mit Hautkrankheiten auf. Das Tier zeigte Hunderte von Papeln, die die “blau” behaarten Bezirke des Felles betrafen. Die vorherrschenden Hautveranderungen bestanden in keratinisierenden infundibularen Zysten, Keratinhornern, perifollikularer Dermatitis und Talgdrusenhyperplasie; diese Veranderungen wurden oft von Furunkulose und eitriger Pannikulitis begleitet. Uber eine Zeitspanne von 9 Monaten wurden 32 Veranderungen histologisch untersucht, wovon zwei in Lipomen bestanden, eine in einem infiltrativen Lipom, eine in einem squamosen Papillom, zwei in Mastzelltumoren, vier in kavernosen Hamangiomen, eine in einem Hamangiosarkom und drei in Melanomen. Es ist zur Zeit nicht bekannt, ob der Phanotyp mit der Farbverdunnung mit einem erhohten Risiko fur Tumoren der Haut und/oder des subkutanen Gewebes einhergeht. [Madewell, B. R., Ihrke, P. J., Griffey, S. M. Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia. (Multiple Hauttumoren bei einem Dobermann mit Farbmutantenalopezie.) Veterinary Dermatology 1997; 8: 59–62.]

Cutaneous vasculitis was identified by histopathological findings in 72 equines. The most frequent clinical findings were crusts/scales and oedema of the legs with the most common underlying disease being photo-aggravated dermatitis. Common laboratory findings were anaemia, neutrophilia, hyperglycaemia and hyperglobulinaemia. Histopathological patterns were most commonly cell-poor and lymphocytic/histiocytic. While statistically supported treatment recommendations could not be made due to the large numbers of confounding factors, trimethoprim-sulfa antibiotics, corticosteroids, and/or resolution or control of the underlying disease process were the most common treatment modalities.

Sporotrichosis is an uncommon to rare cutaneous and subcutaneous mycosis of animals and humans caused by the dimorphic fungus Sporothrix schenckii. Twenty-three mammalian cases of sporotrichosis examined between 1987 and 2007 at the University of California, Davis - Veterinary Medical Teaching Hospital, were retrospectively evaluated with regard to the historical, clinical, diagnostic and treatment findings. Cats were the most common species affected (n = 14). In addition, sporotrichosis was diagnosed in four dogs, four horses and a donkey. Six of 23 cases were diagnosed with the localized cutaneous form of sporotrichosis (four cats, one dog, one horse), 10 with the cutaneous-lymphatic form (four cats, two dogs, three horses and a donkey), and seven with the disseminated form (six cats, one dog). Two of 23 cases did not have skin lesions at the time of diagnosis (one cat, one dog). The most common mode of diagnosis was demonstration of S. schenckii on histopathological evaluation of tissue. In contrast with most previously described sporotrichosis infections in cats, few to no fungal organisms were seen in histopathological samples (haematoxylin and eosin and special stains) in five of the 14 cats. Treatments received included itraconazole (12 cats, one dog), ketoconazole (three dogs), fluconazole (one cat, one donkey), sodium iodide (four horses, one cat) and potassium iodide (one cat, one horse, one donkey). The prognosis for successful treatment was good in all species. Fluconazole was successful in inducing resolution of the cutaneous lesions and controlling the infection in one cat with disseminated sporotrichosis.

A Quarter horse filly bred from two horses affected with HERDA (hereditary equine regional dermal asthenia) was observed clinically and its skin histologically for the 1.5 years of its life. Severe signs of the disease did not manifest until 1.5 years of age, and were not temporally related to saddling. Histological comparison to an age-, breed- and sex-matched control did not show any consistent diagnostic features. Monitoring of the proband substantiated previous reports of (i) the autosomal recessive nature of the disease, (ii) mares affected with HERDA being able to foal without damage to the skin or reproductive tract, (iii) HERDA foals appearing phenotypically normal throughout the first year of life, and (iv) demonstrated that histological interpretation of skin specimens from grossly normal skin may be insufficient to differentiate HERDA-affected horses from controls.

Four new cases of sarcoptic mange in cats are described. Two cats resided in areas known to be frequented by foxes, another cohabited with a dog recently diagnosed with sarcoptic mange, while the final cat lived with a mixed breed dog that had been treated for sarcoptic mange 7 months previously. Three cases were diagnosed on the basis of characteristic mite size and morphology in skin scraping from representative lesions, situated on the head (two cases) or head and distal hind limbs (one case). Mites were highly mobile and abundant in all instances, and easily detected also in skin biopsy specimens procured from two cases. Eosinophilic inflammation, hyperkeratosis and parakeratosis were prominent in the tissue sections. In the remaining case, the diagnosis was presumptive, based on characteristic lesions, cohabitation with a canine scabies patient and positive response to scabicide therapy. Pruritus was not a prominent clinical feature in any patient and was considered to be absent in three of the four cases. Lesions in three cats with long-standing disease were reminiscent of crusted scabies (synonym: Norwegian scabies, parakeratotic scabies) as seen in human patients. In three cases, in-contact human carriers developed itchy cutaneous papular lesions. Two cases responded promptly to therapy with systemic avermectin drugs, while one responded to topical treatment with lime sulphur and the remaining cat received both a lime sulphur rinse and ivermectin. Sarcoptic mange should be considered in the differential diagnosis of cats with non-pruritic crusting skin diseases, especially when there is contact with foxes or dogs, and when owners have itchy papular lesions.

Nine horses from ages 5 to 21 years were diagnosed with cutaneous equine sarcoidosis (ES) over an 18-year period. In addition to skin, the lungs were frequently involved, with other organ systems affected less commonly. A predisposition for thoroughbreds and geldings was noted. Cutaneous lesions and signs included crusts, scales, alopecia and pruritus. These were found at various sites, particularly the legs/thighs/elbows, thorax, neck, face and ventral abdomen. Three horses were euthanized shortly after hospitalization; others survived as long as 12 years. Histopathologic stains, immunohistochemistry and polymerase chain reaction assays on paraffin-embedded cutaneous specimens from eight horses for Mycobacterium spp., Coccidioides immitis, Cryptococcus neoformans, Corynebacterium pseudotuberculosis, and Borrelia burgdorferi were all negative. The aetiology of ES is unlikely microbial and continues to be a diagnosis of exclusion. ES, when limited to the skin, is associated with a good prognosis, with either partial or complete response to glucocorticoid therapy in all the surviving horses.

Data on fifty horses with hereditary equine regional dermal asthenia (HERDA; "hyperelastosis cutis") were collected on clinical, histopathological, ultrastructural and immunohistological findings. All horses were Quarter horses or of Quarter horse ancestry. Pedigree evaluation strongly supported an autosomal recessive mode of inheritance. The most common lesions were seromas/haematomas, open wounds, sloughing skin, and loose, easily tented skin that did not return to its initial position. Definitive diagnosis could not be made via histopathology, although the presence of tightly grouped thin and shortened collagen fibres arranged in clusters in the deep dermis was suggestive of the disease. Trichrome, acid orcein-Giemsa and immunohistochemical stains for collagens I and III showed no consistent abnormalities compared to control horses; an increase in elastic fibres was not a consistent finding. Electron microscopy showed no abnormalities in the periodicity of the collagen bundles; neither orientation nor variation of cross-section diameter of the collagen fibrils differentiated control from affected horses. The diagnosis of HERDA relies on clinical presentation, but may be supported by suggestive (although not pathognomonic) histopathological lesions.

Clinical, morphological and immunohistochemical features of cutaneous lymphocytosis, an uncommon disease histologically resembling well-differentiated malignant lymphoma, were characterized in 23 cats. Clinical outcome was correlated with histomorphology and immunophenotype in an attempt to predict benign vs. malignant behaviour. The disease mainly affected older cats. Lesions were solitary in 61% of cats and often characterized by alopecia (73.9%), as well as erythema, scaling and ulceration. The lateral thorax was most commonly affected (43.5%). Pruritus was frequent (65.2%). Systemic signs included anorexia and weight loss. Morphologically, lesions were characterized by dermal infiltrations of well-differentiated CD3+ T-cells (100%) and aggregates of CD79+ B-cells (64.3%). Cutaneous lymphocytosis is slowly progressive and relatively benign, although in some cats systemic signs led to euthanasia. Four of 12 euthanized cats and one live cat also had lymphoid infiltrates in internal organs. Unfortunately, we were unable to predict clinical outcome by histological and immunohistochemical evaluations of skin lesions.

Forty-one cases of zinc-responsive dermatosis in the dog are described. The Siberian husky was the predominant breed affected. Periocular crusts were the most common clinical sign and parakeratosis was noted in the skin biopsy specimens of all dogs. Treatment with oral zinc ameliorated the clinical signs in most dogs, but cases necessitating other treatments such as parenteral zinc or retinoids are reported. The authors recommend a starting dose of 2-3 mg kg-1 elemental zinc per day in the treatment of this disorder.

Six adult dogs were presented with an unusual bullous dermatosis affecting the glabrous skin of the ventral abdomen and medial thighs. Clinically, flaccid bullae were accompanied by erythema, ulceration, haemorrhage and hyperpigmentation in four of six dogs; the remaining two dogs had thin skin without grossly apparent bullae. Histologically, subepidermal bullae and clefting, vascular proliferation and dilatation (phlebectasia), and alteration in the density and staining of superficial dermal collagen were seen in all dogs. In all cases, corticosteroid-containing topical products had been applied to the affected areas prior to the development of the dermatosis; skin lesions resolved when topical corticosteroids were withdrawn. Follow-up biopsy of three dogs showed resolution of the previously abnormal collagen and subepidermal clefting. Residual lesions included phlebectasia, comedones and hyperpigmentation. The authors postulate that subepidermal clefting was due to local, corticosteroid-induced skin fragility. This is the first report, to our knowledge, of bullous skin disease in dogs resulting from topical corticosteroid therapy.

A paraneoplastic alopecia associated with internal malignancy is reported in four cats. Acute, bilaterally symmetrical, ventral glistening alopecia, weight loss and lethargy were present in all cats. Skin biopsy specimens exhibited severe follicular and adnexal atrophy with follicular miniaturization, minimal inflammation and, in many cases, absence of stratum corneum. At the time of diagnosis, three cats had a metastatic pancreatic adenocarcinoma and one had a bile duct carcinoma. This report confirms, and expands upon the previous report of a syndrome associating ventral alopecia and metastatic visceral carcinomas in cats. Resume— Une alopecie paraneoplasique associee a une tumeur interne maligne est observee sur 4 chats. Les symptomes sont caracterises par une alopecie symetrique et bilaterale sur le ventre avec un aspect brillant et lisse, un amaigrissement, une lethargic Les lesions histopathologiques sont caracterisees par une atrophie folliculaire et annexielle avec des petits follicules pileux, une inflammation dermique discrete et dans beaucoup de cas, une absence du stratum corneum. Trois chats presentent un adenocarcinome pancreatique metastase et un chat un cholangiocarcinome. Ces cas confirment l'existence d'un syndrome associant une alopecie ventrale et des carcinomes visceraux metastatiques chez le chat. [Pascal-Tenorio, A., Olivry, T., Gross, T. L., Atlee, B. A., Ihrke, P. J. Paraneoplastic alopecia associated with internal malignancies in the cat. (Alopecie paraneoplasique associee a des tumeurs malignes internes chez le chat.) Veterinary Dermatology 1997; 8: 47–52.] Resumen Se describe en cuatro gatos una alopecia paraneoplasica asociada a procesos malignos internos. Todos los gatos presentaban una alopecia bilateral, simetrica, ventral, de aspecto brillante, perdida de peso y letargia. Las biopsias cutaneas mostraron atrofia folicular y adnexal marcada, miniaturizacion de foliculos, inflamacion minima y, en muchos casos, ausencia del estrato corneo. En el momento del diagnostico, tres de los gatos tenian un adenocarcinoma metastatico y uno tenia un carcinoma de conducto biliar. Este articulo confirma y amplia un informe previo sobre el sindrome de alopecia ventral y carcinomas viscerales metastaticos en gatos. [Pascal-Tenorio, A., Olivry, T., Gross, T. L., Atlee, B. A., Ihrke, P. J. Paraneoplastic alopecia associated with internal malignancies in the cat. (Alopecia paraneoplasica asociada a procesos malignos internos en el gato.) Veterinary Dermatology 1997; 8: 47–52.] Zusammenfassung— Es wird uber eine paraneoplastische Alopezie in Verbindung mit inneren malignen Prozessen bei vier Katzen berichtet. Bei alien Katzen traten eine akute bilateral symmetrische ventrale Alopezie, Gewichtsverlust und Lethargie auf. Die Hautbiopsien zeigten eine schwere follikulare und adnexale Atrophie mit follikularer Miniaturisation, geringer Entzundung und in vielen Fallen ein Fehlen des Stratum corneum. Zum Zeitpunkt der Diagnose litten drei Katzen an einem metastasierenden Adenokarzinom des Pankreas und eine Katze an einem Gallengangskarzinom. Dieser Bericht erhartet und erweitert den fruheren Bericht uber ein Syndrom, das ventrale Alopezie in Verbindung mit metastasierenden Eingeweidekarzinomen bei der Katze beschreibt. (Paraneoplastische Alopezie in Verbindung mit inneren malignen Prozessen bei der Katze.) Veterinary Dermatology 1997; 8: 47–52.]

Resume— Une urtricaire due a la diethylcarbamazine associee a une dermite prurigineuse a ete suspectee chez un chien mâle castre croise Retriever. L'animal presentait des lesions d'urticaire multiples qui avaient tendance a fusionner au niveau des paupieres, des levres, les conques auriculaires et du prepuce. Les biopsies cutanees ont revele un infiltrat perivasculaire et periannexiel intense riche en polynucleaires eosinophiles. Parfois les polynuclaires eosinophiles etaient “degranules” ou presentaient des formes “en flamme”. La suppression de l'administration de diethylcarbamazine a ete suivie d'une disparission rapide de toutes les lesions cutanees. L'hypothese d'une reaction immune a la diethylcarbamazine est proposee. [Vitale, C. B., Ihrke, P. J., Gross, T. L. Putative diethylcarbamazine-induced uticaria with eosinophilic dermatitis in a dog. (Probable urticaire et dermite eosinophilique induites par la diethylcarbamazine chez un chien). Resumen— Se describe el caso de un perro macho castrado, cruzado de retriever que presentaba una dermatitis pruritica con urticaria supuestamente inducida por dietilcarbamacina. El perro mostraba multiples habones, principalmente alrededor de los ojos, la boca, los pabellones auriculares y el prepucio. El estudio histologico mostro un infiltrado perivascular y perianexal, con predominancia de eosinofilos. Ocasionalmente los eosinofilos degranulaban formando “figuras en llama”. La retirada de la terapia con dietilcarbamacina fue seguida por una mejoria rapida y espectacular de todas las lesiones cutaneas. Se postula una reaccion adversa a la dietilcarbamacina mediada por factores inmunologicos. [Vitale, C. B., Ihrke, P. J. and Gross, T. L. Putative diethylcarbamazine-induced urticaria with eosinophilic dermatitis in a dog (Urticaria con dermatitis eosinofilica supuestamente inducida por dietilcarbamacina en un perro). Zusammenfassung— Es wird uber eine vermutlich Diethylcarbamazin-verursachte Urtikaria mit Juckreiz bei einem mannlich-kastrierten Retrievermischling berichtet. Der Hund wies generalisiert multifokale Striemen auf, die dazu tendierten um Augen, Mund, Ohrmuscheln und Praputium zusammenzulaufen. Die Hautbiopsie zeigte ein starkes perivaskulares und periadenxales Infiltrat mit vorwiegend eosinophilen Granulozyten. Gelegentlich degranulierten die Eosinophilen zu “Flammenform”. Das Absetzen von Diethylcarbamazin fuhrte zu einer dramatischen und raschen Abheilung aller Hautveranderungen. Es wird eine immunologischvermittelte Arzneimittelreaktion auf Diethylcarbamazin vermutet. [Putative diethylcarbamazine-induced utricaria with eosinophilic dermatitis in dogs (Vermutlich Diethylcarbamazin-verursachte Urtikaria mit eosinophiler Dermatitis beim Hund). Abstract— A suspected diethylcarbamazine-induced urticarial dermatitis with associated pruritus is reported in a castrated male mixed breed retriever. The dog had generalized multifocal wheals that tended to cluster around the eyes, mouth, pinnae, and prepuce. Skin biopsy revealed an intense perivascular and periadnexal infiltrate with eosinophils predominating. On occasion, eosinophils degranulated to form “flame figures”. Withdrawal of diethylcarbamazine resulted in dramatic and rapid resolution of all skin lesions. An immunologically mediated adverse drug reaction to diethylcarbamazine is proposed.

The relationship between skin pigmentation and piliation and the development of hemangiomas and hemangiosarcomas in the dermis and subcutaneous tissue was studied in 212 dogs. These 212 dogs had a combined total of 306 tumors; 38 of these 212 dogs had two or more of the same tumor in a different location or a combination of hemangioma and hemangiosarcoma. The average age of the dogs at the time of excision of these tumors was greater than 10 years. There was no sex predilection for the presence or absence of tumors. Cutaneous hemangiomas (73%) were more common than cutaneous hemangiosarcomas (27%). Hemangiomas had no predilection for dermis (51%) or subcutaneous tissue (47%), but hemangiosarcomas had a marked predilection for dermis (73%) over subcutaneous tissue (7%). Dogs with short hair coats and lightly pigmented skin had more hemangiomas and hemangiosarcomas of the dermis (65%) than did dogs with variable length hair coats and pigmentation (28%). Dogs with short hair coats and lightly pigmented skin had fewer hemangiomas and hemangiosarcomas of the subcutaneous tissue (10%) than did dogs with variable length hair coats and pigmentation (22%). Dogs with short hair coats and lightly pigmented skin also had more hemangiomas and hemangiosarcomas of ventral glabrous skin (65%) than did dogs with variable length hair coats and pigmentation (22%). In addition, there was no predilection of subcutaneous hemangiosarcoma for haired (33%) versus glabrous (33%) skin, but dermal hemangiosarcoma had a marked predilection for the glabrous skin (63%) when compared with haired skin (10%). The increased incidence of dermal hemangiomas and hemangiosarcomas in ventral glabrous skin suggests an association between solar radiation and the biologic properties of glabrous skin in the genesis of these tumors.

Background: Equine sarcoidosis is a rare, multisystemic, noncaseating, granulomatous and lymphoplasmacytic disease of unknown etiology. A recent report described a horse with granulomatous skin disease displaying histologic, electron microscopic, and polymerase chain reaction (PCR) findings consistent with equine herpesvirus 2 (EHV-2). Objective: To investigate the presence of EHV-2 and equine herpesvirus 1 (EHV-1) in 8 horses with sarcoidosis. Animals: Eight horses with sarcoidosis, reported previously. Methods: Retrospective study. PCR assays of the tissues were performed to detect DNA associated with EHV-1 and EHV-2. For both herpesviruses the target was their respective glycoprotein B gene. Positive controls consisted of DNA from viral cultures of culturettes from naturally occurring respiratory infections of EHV-1 and EHV-2. Results: The PCR analyses for both equine herpesviruses' DNA were negative in all 8 horses. Conclusion: The failure to detect DNA from EHV-1 and EHV-2 in paraffin-embedded skin of these 8 horses does not discount EHV-1 or EHV-2 as causing some cases of ES, but lends support to the presumably multifactorial etiologic nature of the disease.

Immunostaining with polyclonal anti-Mycobacterium bovis (BCG) was evaluated as a single screen-ing method for the histological identification of micro-organisms in skin biopsy specimens from various veterinary species. Confirmed archival cases infected with Mycobacteria, Nocardia, Actinobacillus, Actinomyces, Streptococcus/Staphylococcus, Dermatophilus, spirochetes, Blastomyces, Coccidioides, Crypto-coccus, Histoplasma, dermatophytes, Malassezia, Sporothrix, Leishmania, Pythium, phaeohyphomycetes and Prototheca organisms were selected. A total of 70 skin biopsy specimens from the dog, cat, horse, ox and llama were evaluated. The anti-BCG immunostain labelled bacteria and fungi with high sensitivity and minimal background staining but did not label spirochetes and protozoa (Leishmania). Differences were not noted between veterinary species. The results indicate that immunostaining with polyclonal anti-BCG is a suitable screening technique for the rapid identification of most common bacterial and fungal organisms in paraffin-embedded specimens. Also, mycobacterial and nocardial organisms were identified more readily with the anti-BCG immunostain in comparison to the histochemical stains.

Human bullous pemphigoid (BP) is an immune-mediated blistering disease characterized by autoantibodies against BP antigens (230/180 kd), which are constitutive glycoproteins of hemidesmosomes found in basal keratinocytes. Blistering diseases similar to human BP have been reported in dogs. IgG deposits at the basement membrane zone (BMZ) are a common feature of canine BP. Although circulating anti-BMZ IgG autoantibodies have been demonstrated in some cases of canine BP, the specific skin protein targeted by these autoantibodies has not been identified. In this study, we characterized the antigenic target of the autoantibodies in the serum from a 3-year-old castrated male Pit Bull Terrier with BP. Direct immunofluorescence of the patient's skin demonstrated IgG deposits at the dermal-epidermal junction. Indirect immunofluorescence demonstrated autoantibodies in the patient's serum that stained the epidermal roof of salt-split canine skin and left the dermal floor unstained. These serum autoantibodies did not stain normal intact dog skin but labeled intact bovine tongue. Direct immunoelectron microscopy of the dog's skin revealed IgG deposits within the hemidesmosomes of the basal keratinocytes. Western immunoblotting experiments showed that canine keratinocytes express both the 230-kd and 180-kd bullous pemphigoid antigens, and the autoantibodies from the patient's serum recognized the 180-kd bullous pemphigoid antigen in proteins extracted from canine and human keratinocytes. Canine BP has many parallel features with human BP including similar immune deposition of IgG within hemidesmosomes and a hemidesmosome-associated 180-kd glycoprotein target for circulating autoantibodies.

Eosinophilic plaque and mosquito-bite dermatitis are recognized hypersensitivity reactions. The pathogenesis of eosinophilic granuloma and indolent ulcer are not as clearly understood. Each of these syndromes is distinctive from a clinical and histopathologic view point. Accurate diagnosis depends on history, physical findings, and histopathologic evaluation. Understanding of feline dermatology will be furthered by including these syndromes in a broader grouping that encompasses all the feline eosinophilic dermatoses.

A previous study described cutaneous lymphocytosis (CL) in 23 cats. The process resembles cutaneous pseudolymphoma in humans, a heterogeneous group of benign reactive proliferations of well-differentiated lymphocytes in the skin of humans. Morphological and immunophenotypic characteristics do not offer reliable criteria to accurately predict the clinical outcome of feline CL or pseudolymphoma in humans. Presence of clonal cell populations is more consistent with a neoplastic process. In a previous study, feline CL lesions (20 cats) were evaluated for clonality using PCR, and only two cats had monoclonal T-cell populations. Because false-negative results may occur, the purpose of this study was to repeat the PCR using a revised primer set based on analysis of additional feline T-cell receptor γ (TCRγ) sequences. DNA was isolated from 29 skin lesions and six internal organs of 20 cats. DNA integrity was assessed by glyceraldehyde-3-phosphate dehydrogenase PCR. Polymerase chain reaction clonality was performed using the revised primer set specific for feline TCRγ, and duplicate samples were evaluated. The PCR products were assessed by heteroduplex analysis. Clonal rearrangement of TCRγ was detected in 14 cats (24 of 35 tissues: 21 of 29 skin lesions and three of six internal organs); eight of these cats are still alive and six were euthanized. Monoclonal populations were seen in three of five cats that had involvement of internal organs. These findings indicate that feline CL is best considered as a slowly progressive process which may be reactive, but often evolves into a low-grade indolent lymphoma. Funding: George H. Muller Fund for Research in Dermatology.

Summary A special buffered ammonium sulfate fixative (Michel's fixative) designed for use as a liquid media capable of preserving in vivo tissue fixed immunoglobulins and complement was evaluated. The preservative ability of this fixative was studied by using skin biopsies from a confirmed case of spontaneously occurring equine pemphigus foliaceus. Once obtained, 16 skin biopsies were placed in Michel's fixative. Eight samples were stored at ambient temperature (21°C) and 8 samples were stored in a conventional refrigerator at 4°C. Over an 8 month time period, direct immunofluorescence was performed on these skin biopsies looking for the abnormal presence of IgG, IgM (when done) and C 3 deposition within the intercellular spaces of the epidermis. The results of this study indicated that Michel's fixative was capable of preserving in vivo tissue fixed immunoglobulin and complement for 8 months. This was demonstrated by positive direct immunofluoresence spaces of the epidermis in all of the skin biopsies examined. In addition, it was shown that refrigerated and non-refrigerated skin biopsies in Michel's fixative both yielded a diagnostic quality of direct immunofluorescence. This will allow the mailing of skin biopsies without requiring refrigeration and specimens mailed in the winter should demonstrate reliable results on fluorescent antibody testing when performed.

Skin biopsy specimens from 7 dogs with immune-mediated skin diseases diagnosed by routine histology and 5 dogs with other skin diseases were placed in Michel's transport medium for 4 to 9 years. Direct immunofluorescence yielded positive results in tissue samples from 3 dogs with pemphigus foliaceus and 2 dogs with discoid lupus erythematosus. Direct immunofluorescence was not seen in tissue samples from 1 dog with pemphigus foliaceus and 5 dogs with non immune-mediated skin diseases. Direct immunofluorescence was seen in skin biopsy specimens maintained in Michel's medium for 4 to 8 years.