一种罕见的持续性 Müllerian 管发育不全综合征：伴有生殖细胞睾丸癌和子宫疝的横位睾丸。

A rare form of persistent Mullerian duct syndrome: Transverse testicular ectopia with germ cell testis cancer and hernia uteri inguinalis.

机构信息

Urology Department, Faculty of Medicine, Recep Tayyip Erdogan University, Rize, Turkey.

Division of Surgical Oncology, General Surgery Department, Faculty of Medicine, Recep Tayyip Erdogan University, Rize, Turkey.

出版信息

Andrologia. 2021 Dec;53(11):e14229. doi: 10.1111/and.14229. Epub 2021 Sep 6.

DOI:10.1111/and.14229

PMID:34490930

Abstract

Persistent Mullerian duct syndrome is a rare form disorder of sexual differentiation characterised by the persistence of Mullerian derivatives (fallopian tubes, uterus and the proximal vagina) in males with an XY karyotype and normal virilisation. We report a case of a 29-year-old man with right transverse testicular ectopia, mix germ cell cancer at ectopic right testis and left-sided obstructed inguinal hernia containing a uterus and fallopian tube. We performed orchiectomy and hysterectomy on the patient.

摘要

持续性 Müllerian 管发育不全综合征是一种罕见的性分化障碍，其特征是在具有 XY 染色体核型和正常男性化的男性中，Müllerian 衍生物（输卵管、子宫和阴道近端）持续存在。我们报告了一例 29 岁男性，右侧横位睾丸异位，异位右侧睾丸混合生殖细胞瘤和左侧腹股沟疝伴阻塞，其中包含子宫和输卵管。我们对患者进行了睾丸切除术和子宫切除术。