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持续性苗勒管综合征

Persistent müllerian duct syndrome.

作者信息

Rizk D E, Ezimokhai M, Hussein A S, Gerami S, Deb P

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.

出版信息

Arch Gynecol Obstet. 1998;261(2):105-7. doi: 10.1007/s004040050208.

Abstract

We report an 18-month old male presenting with a right-sided inguinal hernia and undescended testes. At herniotomy, a uterus and two fallopian tubes were found in the pelvic peritoneum adjacent to the two gonads which received their blood supply partly along the müllerian duct remnants. The gonads were testes by histological examination. Bilateral orchiopexy was performed without removal of the müllerian structures for fear of jeopardizing the testicular blood supply. The diagnosis of persistent müllerian duct syndrome was confirmed postoperatively by genetic and hormonal investigations.

摘要

我们报告一名18个月大的男性,患有右侧腹股沟疝和隐睾。在疝修补术中,在盆腔腹膜中靠近两个性腺处发现了一个子宫和两条输卵管,它们部分沿着苗勒管残余物接受血液供应。通过组织学检查,性腺为睾丸。由于担心危及睾丸血液供应,未切除苗勒管结构而进行了双侧睾丸固定术。术后通过基因和激素检查确诊为持续性苗勒管综合征。

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