卵巢原发性癌肉瘤一罕见肿瘤病例报告并文献复习

R. Patnayak, A. Jena, J. Prakash, R. Sundaram, B. Vijaylaxmi, Amarchala Yadagiri Lakhmi
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引用次数: 3

摘要

摘要原发性卵巢癌肉瘤是一种罕见的双相肿瘤。肿瘤中可见恶性上皮和间质成分的不同混合。我们报告一个72岁绝经后女性原发性卵巢癌肉瘤的病例,主诉腹胀。对该患者进行了分期剖腹手术,最终的组织病理学报告为卵巢癌肉瘤。上皮和肉瘤成分各自的标记物显示免疫组化阳性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary carcinosarcoma of ovary an unusual tumor case report with review of literature
Primary ovarian carcinosarcoma is a rare biphasic tumor. There is variable admixture of both malignant epithelial and stromal component seen in this tumor. We report a case of a primary carcinosarcoma of ovary in a 72-year-old post-menopausal female presenting with the complaint of abdominal distension. Staging laparotomy was done for this patient, and final histopathology was reported as the carcinosarcoma of ovary. The epithelial and sarcomatous components showed immunohistochemical positivity for their respective markers.
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