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副卵巢肾上腺残余瘤:未经治疗的先天性肾上腺增生的妇科表现。

Para-ovarian adrenal rest tumors: gynecologic manifestations of untreated congenital adrenal hyperplasia.

作者信息

Sisto Jessica M, Liu Fong W, Geffner Mitchell E, Berman Michael L

机构信息

a Las Vegas Minimally Invasive Surgery , Las Vegas , NV , USA.

b Department of Gynecology Oncology , Beth Israel Deaconess Medical Center , Boston , MA , USA.

出版信息

Gynecol Endocrinol. 2018 Aug;34(8):644-646. doi: 10.1080/09513590.2018.1441399. Epub 2018 Feb 20.

Abstract

Congenital adrenal hyperplasia (CAH) is an inherited disorder of adrenal steroidogenesis often diagnosed in infancy. Gynecologists may encounter adult patients with CAH due to the clinical effects of increased androgens, e.g. hirsutism, clitoromegaly, oligomenorrhea, or, rarely, pelvic masses. This case report reviews the association of para-ovarian adrenal rest tumors with CAH, and the role of gynecologists in their evaluation and treatment. A 23-year-old woman with CAH (21-hydroxyase deficiency) untreated for the past 5 years presented with a pelvic mass and elevated serum testosterone (1433 ng/dL) and plasma ACTH (1117 pg/mL). Intraoperative findings revealed multiple retroperitoneal masses. Final pathology demonstrated adrenal rest tissue. Para-ovarian and ovarian adrenal rest tumors may present as a rare gynecologic manifestation in patients with untreated CAH.

摘要

先天性肾上腺皮质增生症(CAH)是一种遗传性肾上腺类固醇生成障碍疾病,常在婴儿期被诊断出来。由于雄激素增加的临床影响,如多毛症、阴蒂肥大、月经过少,或罕见的盆腔肿块,妇科医生可能会遇到患有CAH的成年患者。本病例报告回顾了副卵巢肾上腺残余瘤与CAH的关联,以及妇科医生在其评估和治疗中的作用。一名23岁患有CAH(21-羟化酶缺乏症)的女性,在过去5年未接受治疗,出现盆腔肿块,血清睾酮(1433 ng/dL)和血浆促肾上腺皮质激素(ACTH,1117 pg/mL)升高。术中发现多个腹膜后肿块。最终病理显示为肾上腺残余组织。副卵巢和卵巢肾上腺残余瘤可能是未治疗的CAH患者罕见的妇科表现。

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