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甲状腺功能减退症和高脂血症合并未另行特指的男性化卵巢类固醇细胞瘤。

Hypothyroidism and hyperlipidemia with a virilizing ovarian steroid cell tumor, not otherwise specified.

作者信息

Tsai Horng-Jyh, Chen Shu-Chen, Wei Hsiao-Yun, Chen Gin-Den

机构信息

Department of Obstetrics and Gynecology, Chung-Shan Medical University and Hospital, 110 Section 1 Chien-Kuo North Road, Taichung, Taiwan 402.

出版信息

Gynecol Endocrinol. 2007 Feb;23(2):69-71. doi: 10.1080/09513590601137111.

Abstract

Steroid cell tumors, not otherwise specified, are rare ovarian sex cord-stromal tumors with malignant potential. The majority of these tumors produce steroids, with testosterone being the most common. A 44-year-old woman with hypothyroidism and hyperlipidemia presented with abrupt onset of oligomenorrhea, progressive virilization as acne, hirsutism and clitoromegaly, and a non-palpable pelvic mass. The preoperatively elevated serum testosterone level returned to normal after salpingo-oophorectomy, and then menstrual flow became regular.

摘要

未另行分类的类固醇细胞瘤是罕见的具有恶性潜能的卵巢性索间质肿瘤。这些肿瘤大多会产生类固醇,其中睾酮最为常见。一名患有甲状腺功能减退和高脂血症的44岁女性,出现了月经过少的突然发作、痤疮、多毛症和阴蒂肥大等进行性男性化表现,以及一个盆腔内无法触及的肿块。输卵管卵巢切除术后,术前升高的血清睾酮水平恢复正常,随后月经恢复规律。

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