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一名绝经后严重高雄激素血症患者的卵巢莱迪希细胞瘤。

Ovarian Leydig cell tumor in a post-menopausal patient with severe hyperandrogenism.

作者信息

Souto Selma B, Baptista Pedro V, Braga Daniel C, Carvalho Davide

机构信息

Department of Endocrinology, Diabetes and Metabolism, Centro Hospitalar S. João, Porto, Portugal.

Department of Gynecology and Obstetric, Centro Hospitalar S. João, Porto, Portugal.

出版信息

Arq Bras Endocrinol Metabol. 2014 Feb;58(1):68-75. doi: 10.1590/0004-2730000002461.

Abstract

Leydig cell tumors are rare ovarian steroid cell neoplasms. More than 75% of patients show signs of virilization due to overproduction of testosterone. We report a case of an 81-year-old woman with progressive signs of virilization, and presenting vaginal bleeding. Clinical analyses revealed high levels of serum testosterone, delta 4-androstenedione and estradiol, and also inappropriate low levels of gonadotrophins for a post-menopausal woman. Transvaginal ultrasound showed no evidence of ovarian tumor, but pelvic and abdominal computerized axial tomography imaging revealed a left ovarian solid nodule, and no evidence of alteration in the adrenal glands. Total hysterectomy and bilateral salpingoophorectomy were performed. Histopathology and immunohistochemistry confirmed the diagnosis of Leydig cell tumor. After surgery, androgen levels returned to normal, and there was regression of the signs of virilization.

摘要

睾丸间质细胞瘤是一种罕见的卵巢类固醇细胞瘤。超过75%的患者因睾酮分泌过多而出现男性化体征。我们报告一例81岁女性患者,有进行性男性化体征,并伴有阴道出血。临床分析显示血清睾酮、Δ4-雄烯二酮和雌二醇水平升高,且对于一名绝经后女性而言,促性腺激素水平低得不合理。经阴道超声未发现卵巢肿瘤迹象,但盆腔和腹部计算机断层扫描成像显示左侧卵巢有实性结节,肾上腺无改变迹象。实施了全子宫切除术和双侧输卵管卵巢切除术。组织病理学和免疫组织化学确诊为睾丸间质细胞瘤。术后,雄激素水平恢复正常,男性化体征消退。

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