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持续性苗勒管综合征合并不可复性腹股沟疝、双侧隐睾及睾丸肿瘤:1例报告

Persistent müllerian duct syndrome associated with irreducible inguinal hernia, bilateral cryptorchidism and testicular neoplasia: a case report.

作者信息

Yuksel B, Saygun O, Hengirmen S

机构信息

Department of 1st,General Surgery, Ankara Numune Training and Research Hospital, Ankara, Turkey.

出版信息

Acta Chir Belg. 2006 Jan-Feb;106(1):119-20. doi: 10.1080/00015458.2006.11679852.

Abstract

Persistent müllerian duct syndrome is a rare form of male pseudohermaphroditism. A case is reported of normal male appearance with bilateral cryptorchidism and a right irreducible inguinal hernia. On exploration, an uterus with two fallopian tubes and a testicle were found in the hernia sac. The uterus, fallopian tubes and left testicle were en bloc removed. Right orchidopexy and hernia repair were performed. In conclusion, if there is an adult bilateral cryptorchidism, surgeons should take into consideration a persistent müllerian duct syndrome.

摘要

持续性苗勒管综合征是男性假两性畸形的一种罕见形式。本文报告一例病例,患者外观为正常男性,双侧隐睾,右侧腹股沟疝且不能回纳。探查时发现疝囊内有一个子宫、两条输卵管和一个睾丸。将子宫、输卵管和左侧睾丸整块切除。同时进行了右侧睾丸固定术和疝修补术。总之,对于成年双侧隐睾患者,外科医生应考虑持续性苗勒管综合征的可能性。

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