Hernia uterine inguinale: association of Müllerian anomaly with ipsilateral renal agenesis and key points of diagnosis and treatment
10.3760/cma.j.cn115610-20250825-00553
- VernacularTitle:腹股沟子宫疝：米勒管发育异常与单侧肾缺如的关联及诊治要点
- Author:
Fei YUE
1
;
Xianke SI
;
Xi CHENG
;
Jianwen LI
Author Information
1. 上海交通大学医学院附属瑞金医院普通外科 上海市微创外科临床医学中心，上海 200025
- Publication Type:Journal Article
- Keywords:
Hernia;
Hernia uterine inguinale;
Müllerian anomaly;
Mayer-Rokitansky-Küster-Hauser syndrome;
Renal anomaly
- From:
Chinese Journal of Digestive Surgery
2025;24(9):1157-1160
- CountryChina
- Language:Chinese
-
Abstract:
The contents of the female inguinal hernia include abdominal organs such as ovaries and fallopian tubes, and most of these are the result of sliding hernias. However, it is worth noting for surgeons specialized in hernia and abdominal wall surgery that there is a rare clinical diagnosis of hernia uterine inguinale, which is commonly seen in the Müllerian anomaly. Combined with relevant research progress at home and abroad, as well as the clinical experience in the diagnosis and treatment of patients with inguinal uterine hernia caused by Müllerian duct anomaly, the authors systematically introduce the clinical manifes-tations, key diagnosis and treatment points of female Müllerian duct anomaly in the inguinal region.
