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首页> 外文期刊>Oncology, Gastroenterology and Hepatology Reports >Sertoli-Leydig cell tumor of ovary in a young female: A case report and literature review
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Sertoli-Leydig cell tumor of ovary in a young female: A case report and literature review

机译：一名年轻女性卵巢Sertoli-Leydig细胞瘤的病例报告及文献复习

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Sertoli-Leydig cell tumor (SLCT) of the ovary is an exceedingly unusual neoplasm that belongs to a group of sex cord?stromal tumors of the ovary and accounts for less than 0.5% of all primary ovarian neoplasms. We present a case of primary ovarian SLCT in a 21?year?old female who presented with a 6?month history of pelvic pain, acne, hirsuitism and oligomenorrhea with elevated testosterone and dehydroepiandrosterone levels. Ultrasound and contrast computed tomography revealed a well?defined hypervascular heterogeneous solid lesion in the left adnexa. Magnetic resonance imaging demonstrated an ovarian origin of the tumor, which indicated an SLCT on histopathology. In this case, we discuss the multimodality imaging findings of SLCT and its management aspects with a review of the literature.
机译：卵巢的Sertoli-Leydig细胞肿瘤（SLCT）是一种极为罕见的肿瘤，属于一组卵巢性索间质肿瘤，占所有原发性卵巢肿瘤的不到0.5％。我们介绍了一名21岁女性的原发性卵巢SLCT病例，该女性出现了6个月的骨盆疼痛，痤疮，多毛症和少经，睾丸激素和脱氢表雄酮水平升高。超声和对比计算机断层扫描显示左附件有明确定义的超血管异质实体病变。磁共振成像显示肿瘤的卵巢起源，这表明在组织病理学上存在SLCT。在这种情况下，我们通过文献综述来讨论SLCT的多模态成像发现及其管理方面。

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