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持续性苗勒管综合征表现为嵌顿性复发性腹股沟疝伴鞘膜积液。

Persistent Mullerian Duct Syndrome Presenting in an Incarcerated Recurrent Inguinal Hernia with Hydrocele.

作者信息

Pulido Lauren, Iwasiuk Gosta, Sparkuhl Michael, Bui Dang, Springs Haley

机构信息

USA.

出版信息

Urol Case Rep. 2017 Mar 16;12:47-48. doi: 10.1016/j.eucr.2017.02.007. eCollection 2017 May.

Abstract

Hernia uteri inguinalis (HUI) is one of the rarest causes of male pseudo-hermaphroditism worldwide. We report the case of a 49-year-old male with discovery of this anomaly during inguinal hernia repair. A 49-year-old man presented to the clinic for recurrent inguinal hernia with enlarging left scrotum consistent with hydrocele on imaging. Upon exploration of the left groin, the left testis was pulled up into the abdomen, revealing a uterus, fallopian tube, and a second atrophic testis. Despite the rarity of HUI, the differential diagnosis for inguinal hernia with associated cryptorchidism and/or hydrocele should include this rare form of pseudohermaphroditism.

摘要

腹股沟子宫疝(HUI)是全球男性假两性畸形最罕见的病因之一。我们报告一例49岁男性,在腹股沟疝修补术中发现了这种异常情况。一名49岁男性因复发性腹股沟疝伴左侧阴囊增大就诊,影像学检查提示鞘膜积液。探查左侧腹股沟时,发现左侧睾丸被牵拉至腹腔内,可见一个子宫、输卵管以及另一个萎缩的睾丸。尽管HUI罕见,但对于伴有隐睾和/或鞘膜积液的腹股沟疝,鉴别诊断应包括这种罕见的假两性畸形形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d2/5358943/43f7fd168f13/gr1.jpg

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