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Olfactory neuroblastoma in a domestic cat and review of the literature

病理 鼻腔 细胞角蛋白 川东北117 嗜铬粒蛋白A 感觉神经母细胞瘤 组织病理学 岩溶 生物 异细胞增多 免疫组织化学 CD99 医学 波形蛋白 川地34 解剖 细胞凋亡 内科学 生物化学 遗传学 干细胞 程序性细胞死亡 贫血
作者
Bernat Martí‐García,Simon L. Priestnall,Emma Holmes,Alejandro Suárez‐Bonnet
出处
期刊:Veterinary Clinical Pathology [Wiley]
卷期号:52 (3): 521-526 被引量:5
标识
DOI:10.1111/vcp.13255
摘要

Abstract Nasal tumors account for less than 10% of all feline neoplasms, with lymphoma, followed by adenocarcinoma, and squamous cell carcinoma, the most commonly reported. Nasal neuroectodermal tumors, including olfactory neuroblastoma (ONB), are scarcely described, and their tumorigenesis is largely unknown. Here we report the cytological, histological, and immunohistochemical features of a feline ONB. We also provide a pathological review of nasal neuroendocrine neoplasms in cats. A 7‐year‐old Burmese cat was evaluated for sneezing, occasional epistaxis, and upper respiratory noise for 8 months. Computed tomography (CT) imaging revealed a 7 × 5 × 3 mm irregular mass effacing and expanding the nasal cavity, which extended to the nasopharynx. Cytologically, neoplastic cells were round to polygonal and had a round nucleus with finely stippled chromatin, a single small nucleolus, and abundant pale blue cytoplasm, which contained abundant fine pale pink granules. They exhibited mild cellular atypia, anisocytosis, and mild to occasionally moderate anisokaryosis. Rhinoscopic biopsies revealed a densely cellular, malignant neuroepithelial neoplasm. Cells were arranged in densely packed trabeculae and formed Homer Wright and Flexner–Wintersteiner‐like rosettes, with rare mitotic figures and scant supportive fibrovascular stroma. Immunohistochemically, neoplastic cells were positive for vimentin, cytokeratin AE1/AE3, COX‐2, and beta‐tubulin and negative for S‐100, chromogranin A, CD117, and epithelial membrane antigen (EMA). An ONB was diagnosed based on histological and immunohistochemical findings. Interestingly, and similar to nasal carcinomas, neoplastic cells diffusely neo‐expressed COX‐2. To the authors′ knowledge, there is no previous evidence of COX‐2 in feline ONB. Histopathology and immunohistochemistry are required for a definitive diagnosis of ONB.

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