Peer-reviewed veterinary case report
Malignant pilomatricoma tumor in a Wheaten Terrier dog
By Jackson, Karen et al.·Published in Veterinary clinical pathology·2010·Department of Pathobiology, United States·View original on PubMed →
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Original publication title: Malignant pilomatricoma in a soft-coated Wheaten Terrier.
- Species:
- dog
Plain-English summary
A 3-year-old male soft-coated Wheaten Terrier was brought in for mild lameness, fecal incontinence, and pain in the lower back. An MRI revealed a large mass in the pelvic area that was affecting the bones and surrounding structures. Unfortunately, tests showed that the mass was a malignant pilomatricoma, a type of tumor, and the owner chose to euthanize the dog due to the poor prognosis. During the necropsy, it was found that the cancer had spread to the lungs as well.
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Abstract
A 3-year-old, castrated male, soft-coated Wheaten Terrier was presented for evaluation of mild lameness, fecal incontinence, lumbosacral pain, and lack of anal tone. Magnetic resonance imaging scan showed a large (8 x 6 x 5 cm) mass invading and expanding the pelvic bones, sacrum, and associated structures. A fine-needle aspirate of the mass contained many neoplastic cells with high nuclear to cytoplasmic ratios and rare spindle and inflammatory cells. The neoplastic cells were 12-16 mum in diameter, round to cuboidal, basaloid in appearance, and arranged both individually and in loosely cohesive clusters with variably distinct cell borders. Given the location, signalment, and cytologic findings, differential interpretations included a primitive embryonal tumor (eg, neuroblastoma or nephroblastoma in an atypical location) or poorly differentiated carcinoma. The owner elected euthanasia due to the poor prognosis. Abnormal gross findings on necropsy included the pelvic mass and multiple firm, pale, pink-tan nodules in the lung, which proved to be metastases. On histologic examination, the mass and nodules were composed of irregular islands, lobules, and nests of basaloid cells, which transitioned abruptly into large lakes of "ghost" cells with areas of ossification and calcification, consistent with a diagnosis of malignant pilomatricoma. This unusual presentation of a pilomatricoma adds to our knowledge of expected cytologic findings for this tumor.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19886971/