Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina. Secondary sexual characteristics and karyotype are normal. This syndrome affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently...

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Published in:African Journal of Urology
Main Authors: L.E. Mubenga, J. Lambertz, A Feyaerts, P Van Cangh, F.X. Wese
Format: Article
Language:English
Published: SpringerOpen 2013-12-01
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1110570413000787
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author L.E. Mubenga
J. Lambertz
A Feyaerts
P Van Cangh
F.X. Wese
author_facet L.E. Mubenga
J. Lambertz
A Feyaerts
P Van Cangh
F.X. Wese
author_sort L.E. Mubenga
collection DOAJ
container_title African Journal of Urology
description Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina. Secondary sexual characteristics and karyotype are normal. This syndrome affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently associated with other malformations (MRKH type II). We present a typical case of MRKH type II associated with bilateral pelvic kidneys ectopia, ureteropelvic junction (UPJ) obstruction and high inserting ureters. The ureteral switch was performed at the time of pyeloplasty to prevent postoperative obstruction secondary to the angulation.
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spelling doaj-art-e2afbf17f9af48a5b4b11f6c1227fffe2025-08-19T19:21:57ZengSpringerOpenAfrican Journal of Urology1110-57042013-12-0119418819010.1016/j.afju.2013.07.005Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeL.E. MubengaJ. LambertzA FeyaertsP Van CanghF.X. WeseMayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina. Secondary sexual characteristics and karyotype are normal. This syndrome affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently associated with other malformations (MRKH type II). We present a typical case of MRKH type II associated with bilateral pelvic kidneys ectopia, ureteropelvic junction (UPJ) obstruction and high inserting ureters. The ureteral switch was performed at the time of pyeloplasty to prevent postoperative obstruction secondary to the angulation.http://www.sciencedirect.com/science/article/pii/S1110570413000787Mayer-Rokitansky-Küster-Hauser syndromeUreteral switch
spellingShingle L.E. Mubenga
J. Lambertz
A Feyaerts
P Van Cangh
F.X. Wese
Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
Mayer-Rokitansky-Küster-Hauser syndrome
Ureteral switch
title Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
title_full Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
title_fullStr Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
title_full_unstemmed Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
title_short Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
title_sort ureteral switch for bilateral ureteropelvic junction obstruction in a case of mayer rokitansky kuster hauser mrkh syndrome
topic Mayer-Rokitansky-Küster-Hauser syndrome
Ureteral switch
url http://www.sciencedirect.com/science/article/pii/S1110570413000787
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