XY性腺发育不全——生殖细胞肿瘤的发生：病例报告
XY gonadal dysgenesis--development of a germ cell tumor: case report.
作者信息
Diessner J, Stüber T, Niederle B, Pawlik M, Dietl J, Honig A
机构信息
Department of Obstetrics and Gynecology, Universitäts-Frauenklinik Würzburg, Würzburg, Germany.
出版信息
Eur J Gynaecol Oncol. 2013;34(6):572-4.
PMID:24601055
Abstract
Gonadal dysgenesis (GD) is a rare congenital malformation that affects about one in 3,000 births. The authors present a case of a 17-year-old woman with primary amenorrhea and poor breast development. They conducted a laparoscopic surgery and bilaterally removed hypoplastic streak gonads. Histopathology of the ovaries revealed bilateral streak gonads with gonadoblastomas and a right-sided dysgerminoma.
摘要
性腺发育不全（GD）是一种罕见的先天性畸形，每3000例出生中约有1例受影响。作者报告了一例17岁原发性闭经且乳房发育不良的女性病例。他们进行了腹腔镜手术，双侧切除发育不全的条索状性腺。卵巢组织病理学显示双侧条索状性腺伴有性腺母细胞瘤和右侧无性细胞瘤。
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