Multiple viral plaques with sebaceous differentiation associated with an unclassified papillomavirus type in a cat. Issue 4 (4th July 2017)

• Record Type: Journal Article
• Authors: Munday, JS; Marshall, S; Thomson, NA; Kiupel, M; Heathcott, RW; French, A
• Is Part Of: New Zealand veterinary journal. Volume 65:Issue 4(2017)
• Page Start: 219
• Page End: 223
• Publication Date: 2017-07-04
• Subjects: Cat -- feline viral plaque -- papillomavirus -- Bowenoid in situ carcinoma -- neoplasia -- skin -- dermatology; Veterinary medicine -- Periodicals; Médecine vétérinaire -- Périodiques; 636.089
• DOI: 10.1080/00480169.2017.1313146
• Languages: English
• ISSNs: 0048-0169

Abstract

Abstract: CASE HISTORY AND CLINICAL FINDINGS: A 15-year-old neutered male domestic short-haired cat was presented due to multiple 0.5–2 cm-diameter crusting plaques in the left preauricular region, over the bridge of nose, and in the right periocular region. The plaques did not appear to cause discomfort. HISTOPATHOLOGICAL FINDINGS: Biopsy samples of four plaques were examined histologically. Three plaques consisted of well-demarcated foci of mild epidermal hyperplasia overlying markedly hyperplastic sebaceous glands. Approximately 60% of the hyperplastic cells contained a large cytoplasmic vacuole that ranged from being clear to containing prominent grey-blue fibrillar material. The fourth plaque was composed solely of epidermal hyperplasia, consistent with previous descriptions of feline viral plaques. MOLECULAR BIOLOGY: Papillomavirus DNA was amplified from all four plaques using PCR. A single DNA sequence was amplified from the plaques with sebaceous differentiation. This sequence was identical to the FdPV-MY sequence previously suggested to be from a putative unclassified papillomavirus type. Felis catus papillomavirus type 2 sequences were amplified from the plaque typical of feline viral plaques. Immunohistochemistry to detect p16 CDKN2A protein (p16) showed marked immunostaining throughout the hyperplastic epidermis and adnexal structures within the plaques with sebaceous differentiation. DIAGNOSIS: Multiple feline viral plaques with variable sebaceous differentiation. CLINICAL RELEVANCE: Feline viral plaques with sebaceous differentiation have not been previously reported in cats. The presence of unique cell changes within these lesions, the detection of an unclassified papillomavirus type, and the p16 immunostaining within these plaques suggest that they may have been caused by the papillomavirus that contains the FdPV-MY sequence.