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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Sertoli -Leydig Cell Tumor of Ovary-A Diagnostic Dilemma
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Sertoli -Leydig Cell Tumor of Ovary-A Diagnostic Dilemma

机译：Sertoli-Leydig卵巢细胞肿瘤-A诊断困境

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摘要

Sertoli Leydig Cell Tumours (SLCTs) are rare, unilateral, sex cord stromal tumours of ovary, which constitute less than 1% of all the ovarian neoplasms. These tumours can be functionally diverse and they may have heterologous elements. We aim to report a case of a 25-year- old woman who presented with suprapubic pain of 5 days duration, a unilateral adnexal mass, hypertestosteronism without virilization. Intraoperative frozen section of the unilateral salpingo-oophorectomy specimen was suggestive of granulosa cell tumour. Histopathological examination, supplemented with alpha-inhibin immunohistochemistry, was diagnostic of Meyer?s type II SLCT. Clinical presentation, pathology and the diagnostic pitfalls in the present case have been presented with a brief review of literature.
机译：Sertoli Leydig细胞瘤（SLCT）是罕见的卵巢单侧性性间质基质肿瘤，仅占所有卵巢肿瘤的不到1％。这些肿瘤在功能上可以多样，并且可以具有异源元件。我们的目标是报告一名25岁女性，其持续时间为5天的耻骨上疼痛，单侧附件包块，睾丸肥大而无病。单侧输卵管卵巢切除术标本的术中冰冻切片提示颗粒细胞瘤。组织病理学检查，加上α-抑制素免疫组织化学，可诊断Meyer II型SLCT。通过简要回顾文献介绍了本病例的临床表现，病理学和诊断缺陷。

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