2022
DOI: 10.1111/vcp.13124
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Duodenal leiomyosarcoma in a cat: Cytologic, pathologic, and immunohistochemical findings

Abstract: A 7‐year‐old mixed‐breed neutered male cat was presented with a history of chronic vomiting with increased frequency in the last month, progressing to depression and profuse projectile vomiting. Abdominal ultrasonography revealed an area of marked segmental duodenal thickening associated with a nodule, and euthanasia was performed due to a poor prognosis. Grossly, at the postmortem examination, the wall of a duodenal segment was severely expanded by a nodule measuring 5.0 cm in diameter, resulting in marked lu… Show more

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Cited by 4 publications
(12 citation statements)
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“…Morphological and molecular genetic findings in feline intestinal carcinomas have been described in detail by Groll and colleagues [29]. Furthermore, mast cell tumours [30][31][32][33] and sarcomas [34][35][36][37][38] have been reported in the feline gastrointestinal tract.…”
Section: Introductionmentioning
confidence: 90%
“…Morphological and molecular genetic findings in feline intestinal carcinomas have been described in detail by Groll and colleagues [29]. Furthermore, mast cell tumours [30][31][32][33] and sarcomas [34][35][36][37][38] have been reported in the feline gastrointestinal tract.…”
Section: Introductionmentioning
confidence: 90%
“…1 Surgery is the recommended treatment of choice and the prognosis depends on the anatomical location of the tumour and the presence of metastasis. [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16] To the authors' knowledge, this report describes a novel diagnosis of retropharyngeal leiomyosarcoma in a young cat with a good outcome following marginal surgical excision. This tumour should be considered as a differential diagnosis for a retropharyngeal mass in the cat.…”
Section: Introductionmentioning
confidence: 83%
“…Chromatin was finely stippled to coarsely clumped with 1–3 small nucleoli per cell. Neoplastic cells exhibited moderate to marked anisocytosis and anisokaryosis with a mitotic count of 1 per 10 high-power fields at × 200 magnification and an area of 2.37 mm 2 ( Figure 4 ). Immunohistochemistry revealed diffuse strong staining of the neoplastic cells with antivimentin (1:500 dilution [Monoclonal Mouse Anti-Human Vimentin Clone; Dako]), antidesmin (1:100 dilution [Monoclonal Mouse Anti-Human Desmin Clone; Dako]) and anti-alpha smooth muscle actin (1:100 dilution [Monoclonal Mouse Anti-Human Smooth Muscle Actin Clone; Dako]) antibodies at × 200 magnification ( Figures 5 and 6 ), consistent with a leiomyosarcoma.…”
Section: Case Descriptionmentioning
confidence: 99%
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