Peer-reviewed veterinary case report
Dog develops dark skin plaques and cancer from new papillomavirus
By Munday, John S et al.·Published in Veterinary dermatology·2011·Department of Pathobiology·View original on PubMed →
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Original publication title: Development of multiple pigmented viral plaques and squamous cell carcinomas in a dog infected by a novel papillomavirus.
- Species:
- dog
Plain-English summary
A 7-year-old mixed-breed dog developed numerous dark, pigmented skin plaques that grew rapidly and eventually turned into squamous cell carcinomas (a type of skin cancer). The dog had these plaques on its belly and under its arms, and despite the skin issues, it appeared otherwise healthy. Over two years, the dog underwent five surgeries to remove 23 ulcerated masses, all of which were confirmed to be cancerous. The presence of a novel papillomavirus (a virus that can cause skin lesions) was identified, which may have contributed to the unusual growth and cancer development.
People also search for: dog skin cancer treatment · papillomavirus in dogs · dog skin plaques causes · squamous cell carcinoma in dogs · mixed-breed dog skin problems
Abstract
Canine viral plaques are uncommon skin lesions that are induced by papillomaviruses (PVs). Plaques are usually of little clinical significance in dogs, although they have been reported rarely to progress to squamous cell carcinoma (SCC). Here is described a 7-year-old mixed-breed dog that developed numerous darkly pigmented plaques up to 8 cm in diameter. Multiple ulcerated nodular masses were visible within plaques on the ventrum and axilla. The dog showed no clinical evidence of immunodeficiency and appeared otherwise healthy. Over the next 2 years, five surgeries were performed to remove 23 ulcerated masses that ranged in size from 2 to 5 cm in diameter. Five masses were submitted for histology, and all were SCCs. Each was surrounded by epidermis that contained histological features consistent with those described in canine plaques. Suggestive of a PV aetiology, massive numbers of large keratohyaline granules were present throughout the thickened epidermis. Additionally, koilocytes were focally present, and one sample contained a band of keratinocytes within the superficial epidermis that contained pale cytoplasm and marginated chromatin. From two samples, DNA sequences from a previously unreported PV were amplified, and immunohistochemistry confirmed the presence of PV antigen in both. The PV DNA sequences were most similar to those of canine PVs previously associated with plaque formation. The plaques observed in this case were unusual owing to their rapid growth, large size and frequent malignant transformation. It is unknown whether this unusual behaviour was due to the specific PV detected in this case or to host factors within the dog.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/20604909/