罕见的生殖细胞瘤的表现:持续性勒氏管综合征

IF 0.1 Q4 ONCOLOGY Uroonkoloji Bulteni-Bulletin of Urooncology Pub Date : 2017-09-28 DOI:10.4274/UOB.825
A. Beksac, M. Dönmez, Ç. Aydın, D. Baydar, M. Yazıcı, A. Ergen, B. Akdogan
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引用次数: 0

摘要

持续性马勒氏管综合征(PMDS)被定义为在表型和核型男性中存在马勒氏残余(1)。PMDS是由缺乏抗马勒氏激素、受体不敏感或马勒氏抑制因子(MIF)释放时间缺陷引起的。由于存在子宫,PMDS被认为是假雌雄同体的一种形式,并被证明是常染色体隐性遗传(2)。虽然它主要见于儿科年龄组,表现为伴有或不伴有腹股沟疝的隐睾,但在成年期可能表现为腹股沟或腹内肿块(3)。在此,我们报告了2例PMDS并回顾了文献。案例展示
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A Rare Presentation of Germ Cell Neoplasia: Persistant Müllerian Duct Syndrome
Persistent Müllerian duct syndrome (PMDS) is defined as the presence of Müllerian remnants in a phenotypically and karyotypically male (1). PMDS is caused either by the lack of anti-Müllerian hormone, receptor insensitivity or a defect in the timing of the release of Müllerian inhibiting factor (MIF). PMDS is regarded as a form of pseudohermaphroditism due to presence of uterus and is shown to be inherited autosomal recessively (2). Although it is predominantly seen in pediatric age group presenting as undescended testis with or without inguinal hernia, it might be presented as an inguinal or intraabdominal mass in adulthood (3). Herein we report 2 cases of PMDS with review of the literature. Case Presentations
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