Dysgerminoma with Estrogen-Producing Functioning Stroma Presenting Precocious Puberty.

IF 0.7 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2021-04-22 eCollection Date: 2021-01-01 DOI:10.1155/2021/5545645
Shunsuke Nagase, Kanako Ogura, Karin Ashizawa, Nana Nakazawa-Tanaka, Masahiko Urao, Masaharu Fukunaga, Yuto Yamazaki, Hironobu Sasano, Toshiharu Matsumoto
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引用次数: 1

Abstract

Dysgerminoma is a malignant ovarian germ cell tumor, and unlike sex-cord stromal tumors, endocrine manifestation is considered rare. Here, we report the first case of dysgerminoma presenting precocious puberty. The patient is a 7-year-old girl who presented with a breast development in Tanner stage 3. Serum estradiol (E2) was markedly elevated while luteinizing hormone (LH) and follicle-stimulating hormone (FSH) were suppressed below the detection limit. Microscopically, the right ovarian mass displayed nests of large polygonal cells and fibrous septa which were focally concentrated by theca-like plump spindle cells. Immunohistochemistry revealed that the spindle cells expressed various steroidogenic enzymes involved in estrogen biosynthesis including P450 aromatase. The tumor was diagnosed with pure dysgerminoma with estrogen-producing functioning stroma. After the operation, serum E2 declined below the detection limit; LH and FSH returned within the normal range. This case demonstrates that even a conventional dysgerminoma can present endocrine manifestation through functioning stroma.

Abstract Image

Abstract Image

伴有雌激素分泌功能基质的生殖细胞异常瘤表现为性早熟。
异常生殖细胞瘤是一种恶性卵巢生殖细胞瘤,与性索间质瘤不同,其内分泌表现被认为是罕见的。在此,我们报告第一例表现为性早熟的异常生殖细胞瘤。患者是一名7岁女孩,表现为坦纳病3期乳房发育。血清雌二醇(E2)明显升高,黄体生成素(LH)和卵泡刺激素(FSH)均被抑制在检测限以下。镜下,右侧卵巢肿块可见巨大的多边形细胞巢和纤维间隔,其中有乳泡状的丰满梭形细胞集中。免疫组化显示梭形细胞表达多种参与雌激素生物合成的甾体生成酶,包括P450芳香化酶。该肿瘤被诊断为纯粹的生殖细胞异常瘤,伴有雌激素生成功能基质。术后血清E2降至检测限以下;LH和FSH恢复正常。本病例表明,即使是常规的生殖异常瘤也可以通过功能性间质表现出内分泌表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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