Retro-Iliac Ureter: A Case Report of an Unusual Cause of Mid-ureteric Obstruction

Retro-iliac ureter, a rare congenital anomaly in which the ureter courses behind the iliac vessels, is infrequently reported in the urological literature. We describe the case of a 27-year-old woman with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type II who presented with recurrent urinary tract infections (UTIs) and persistent right flank pain. Intraoperative retrograde pyelogram (RGP) demonstrated a markedly dilated right ureter with contrast hold-up near the sacroiliac joint. Surgical exploration confirmed a retro-iliac course of the ureter. The patient underwent successful anterior transposition and anastomosis of the ureter. This case illustrates the diagnostic challenges and surgical management of the retro-iliac ureter, particularly when associated with complex congenital anomalies such as MRKH syndrome. To our knowledge, this may be the first reported case of these two rare anomalies being combined.

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Publication Details

Journal
Cureus
Published
2025-09-29
DOI
https://doi.org/10.7759/cureus.93525
Primary Topic
Ureteral procedures and complications
Type
article
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article

Retro-Iliac Ureter: A Case Report of an Unusual Cause of Mid-ureteric Obstruction

Souvik Chatterjee, Debansu Sarkar, Zochampuia Ralte
Cureus
Ureteral procedures and complications
article

Retro-Iliac Ureter: A Case Report of an Unusual Cause of Mid-ureteric Obstruction

Souvik Chatterjee, Debansu Sarkar, Zochampuia Ralte
article en

Abstract

Retro-iliac ureter, a rare congenital anomaly in which the ureter courses behind the iliac vessels, is infrequently reported in the urological literature. We describe the case of a 27-year-old woman with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type II who presented with recurrent urinary tract infections (UTIs) and persistent right flank pain. Intraoperative retrograde pyelogram (RGP) demonstrated a markedly dilated right ureter with contrast hold-up near the sacroiliac joint. Surgical exploration confirmed a retro-iliac course of the ureter. The patient underwent successful anterior transposition and anastomosis of the ureter. This case illustrates the diagnostic challenges and surgical management of the retro-iliac ureter, particularly when associated with complex congenital anomalies such as MRKH syndrome. To our knowledge, this may be the first reported case of these two rare anomalies being combined.

CureusVol. 17(9)
Institute of Post Graduate Medical Education and Research (IN)
Openalex Percentile: Top 66%
Ureteral procedures and complications
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