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犬卵巢无性细胞瘤诱导性性腺母细胞瘤与两种不同类型乳腺癌同时发生:一例病例报告及文献综述

Co-Occurrence of Ovarian Dysgerminoma-Inducing Gonadoblastoma and Two Distinct Mammary Carcinomas in a Dog: A Case Report and Review of the Literature.

作者信息

Golchin Diba, Sasani Farhang, Farzad-Mohajeri Saeed, Tovhidifar Mohsen, Ashrafi Tamai Iradj

机构信息

Department of Pathology and Clinical Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

出版信息

Vet Med Sci. 2025 Jul;11(4):e70470. doi: 10.1002/vms3.70470.

Abstract

Gonadoblastoma (GB) is an extremely rare mixed gonadal neoplasm, encountered in animals as well as humans. The tumour is typically reported in dysgenetic gonads of those suffering from disorders of sex development and bearing the Y chromosome. Here we highlight the first report of the co-occurrence of an ovarian dysgerminoma-inducing GB and anaplastic and complex carcinomas of distinct mammary glands in a phenotypically normal 12-year-old intact female Spitz lacking the Y chromosome. Germ cells of GB and dysgerminoma were negative for c-kit but immunolabelled with SALL4, OCT-4, and E-cadherin and aberrantly expressed WT-1. Sex cord-stromal cells were immunoreactive for α-inhibin, cytokeratin AE1/AE3, and WT-1. Diffuse vimentin immunostaining was observed, while all cells were negative for high molecular weight cytokeratins. The Ki67 index was 30%. We describe the histopathological and immunohistochemical features of the index case and the polymerase chain reaction analysis of the amelogenin (AMEL) gene and provide a review of the literature. The mechanism of GB development may vary in patients with normal karyotypes and dysgenetic individuals. The WT-1 gene mutation may also play a role in the development of GB in the present case.

摘要

性腺母细胞瘤(GB)是一种极其罕见的混合性性腺肿瘤,在动物和人类中均有发现。该肿瘤通常见于患有性发育障碍且携带Y染色体者的发育异常性腺中。在此,我们重点介绍首例关于在一只表型正常、无Y染色体的12岁未绝育雌性斯皮茨犬中,同时出现诱导卵巢无性细胞瘤的GB以及不同乳腺的间变性和复杂性癌的报告。GB和无性细胞瘤的生殖细胞c-kit呈阴性,但SALL4、OCT-4和E-钙黏蛋白免疫染色呈阳性,且WT-1异常表达。性索间质细胞对α-抑制素、细胞角蛋白AE1/AE3和WT-1呈免疫反应性。观察到波形蛋白弥漫性免疫染色,而所有细胞高分子量细胞角蛋白均为阴性。Ki67指数为30%。我们描述了该病例的组织病理学和免疫组化特征以及釉原蛋白(AMEL)基因的聚合酶链反应分析,并对文献进行了综述。GB的发生机制在核型正常的患者和发育异常个体中可能有所不同。WT-1基因突变在本病例GB的发生中可能也起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d1d/12185996/3132929a7725/VMS3-11-e70470-g004.jpg

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