Hernia uterine inguinale with endometriosis in adult Mayer Rokintasky Kuster Hauser syndrome

R Padmasri,Rupa S Iyengar

doi:10.4038/sljog.v35i4.6591

Abstract

A young 25 year old woman presented with primary infertility and was found to have a big left inguinal mass with a blind vagina. Based on the findings of magnetic resonance imaging, a history of probable primary amenorrhea and absence of cervix on clinical examination she was diagnosed as MRKH with inguinal herniation of uterus and adnexae. Operative findings showed bilateral grossly distorted inguinal masses with evidence of endometriosis. Postoperative pathology findings demonstrated endometriosis. DOI: <a href="http://dx.doi.org/10.4038/sljog.v35i4.6591">http://dx.doi.org/10.4038/sljog.v35i4.6591</a> Sri Lanka Journal of Obstetrics and Gynaecology 2013; 35: 122-124

Highlights

A young 25 year old woman presented with primary infertility and was found to have a big firmed speculum examination
Introduction of hypoplastic uterine horns containing with history of primary infertility and endometrium with herniation of these
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype

Summary

Introduction

A young 25 year old woman presented with primary infertility and was found to have a big firmed speculum examination. Operative findings showed bilateral grossly distorted inguinal masses with evidence of within normal limits. Introduction of hypoplastic uterine horns containing with history of primary infertility and endometrium with herniation of these The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype.

Results

Conclusion