Peer-reviewed veterinary case report
Hepatosplenic T-cell lymphoma diagnosis in a dog with spleen
By Cienava, Elizabeth A et al.·Published in Veterinary clinical pathology·2004·Department of Veterinary Pathobiology, United States·View original on PubMed →
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Original publication title: Morphologic, immunohistochemical, and molecular characterization of hepatosplenic T-cell lymphoma in a dog.
- Species:
- dog
Plain-English summary
A 13-year-old neutered male Jack Russell Terrier was brought to the vet because he was lethargic, depressed, vomiting, and had a fever. Tests showed he had low blood platelets and anemia, and a physical exam revealed a swollen spleen. Unfortunately, after surgery to remove the spleen, his condition worsened quickly, leading to euthanasia. Further tests confirmed he had T-cell lymphoma, a type of cancer affecting his spleen and liver.
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Abstract
A 13-year-old neutered male Jack Russell Terrier (Parson Russell Terrier) was presented to the Texas Veterinary Medical Center with a history of lethargy, depression, vomiting, and fever. The dog had mildly regenerative anemia, severe thrombocytopenia and low antithrombin activity. Marked splenomegaly was found on physical examination and imaging studies, and malignant round cell neoplasia and marked extramedullary hematopoiesis were diagnosed on aspirates of the spleen. The dog underwent exploratory laporatomy and splenectomy. Because of a rapid decline in clinical condition postsurgery, the dog was euthanized. Splenic and hepatic biopsies were submitted for histopathologic evaluation. A neoplastic population of round cells was found throughout the splenic parenchyma and within hepatic sinusoids. The neoplastic cells stained strongly positive for CD3 (T-cell marker) and were negative for CD79a (B-cell marker) and lysozyme (histiocytic marker). A diagnosis of T-cell lymphoma was confirmed by assessment of T-cell clonality using canine-specific polymerase chain reaction-based techniques. Although expression of the gammadelta T-cell receptor was not evaluated, this case shares many similarities with a rare syndrome in humans known as hepatosplenic gammadelta T-cell lymphoma.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/15195270/