Maloku Halit, Shabani Ragip, Haliti Naim, Shabani Nora, Maxhuni Qenan, Ferizi Rrahman
University of Prishtina, Faculty of Medicine, Department of Surgery, Prishtina, Kosovo, 10000, Albania.
University of Prishtina, Faculty of Medicine, Department of Pathology Anatomy, Prishtina, Kosovo, 10000, Albania.
Urol Case Rep. 2021 Apr 3;38:101673. doi: 10.1016/j.eucr.2021.101673. eCollection 2021 Sep.
We report the case of a 67-year-old man, father of 3 children with left indirect inguinal hernia containing uterus with cervix, fallopian tube and an ovary attached to the testicle, also spread ovarian tissue and right congenital cryptorchidism. Coincidentally detected during an operation for left inguinal hernia. Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism detected coincidently during surgical operation on cryptorchidism or inguinal hernia.
我们报告了一例67岁男性病例,他是3个孩子的父亲,患有左侧间接性腹股沟疝,疝内容物为带有宫颈的子宫、输卵管以及附着于睾丸的一个卵巢,同时还伴有卵巢组织播散和右侧先天性隐睾症。该病例在左侧腹股沟疝手术中偶然被发现。持续性苗勒管综合征是一种罕见的男性假两性畸形,在隐睾症或腹股沟疝手术中偶然被检测到。