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Citation: Al Adimi A, Odaini N. Urinary retention: A rare presentation of adult ureterocele. Jr. med. res. 2023; 6(1):12-14. Al Adimi et al © All rights
are reserved. https://doi.org/10.32512/jmr.6.1.2023/12.14 Submit your manuscript:www.jmedicalresearch.com
Al Adimi Abdulelah
1
, Odaini Nabil
1*
.
Urinary retention: A rare presentation of adult ureterocele.
1: Department of urology, Al Emadi
Hospital, Doha, Qatar.
* Corresponding author
Correspondence to:
nbilodainil@hotmail.com
Publication Data:
Submitted: November 8,2022
Accepted: December 30,2022
Online: January 31,2023
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Ureterocele is a rare congenital malformation characterized by pseudo-cystic dilation of the
lower ureter extremity [1]. Ectopic ureteroceles is usually a pediatric entity diagnosed
incidentally or in the investigation of childhood urinary tract infection. Diagnosis in adult age
remains rare. Adult ureterocele is characterized by its clinical polymorphism and manifest
obstructive symptomatology in case of complications. We herein report the case of giant
adult ureterocele responsible of complete urinary retention. The aim was to highlight the
clinical, radiological and endoscopic features of this rare condition.
Keywords
Ureterocele; adult; endoscopy; urine retention.
Introduction
Ureterocele is a congenital cystic dilation of the distal ureter out-pouching into the urinary
bladder. Clinical presentation is nonspecific and polymorph leading sometimes to diagnostic
delay. Adult ureterocele is a rare condition and usually asymptomatic. Management of these
cases is challenging and remains nonconsensual [1].
In this report, we present a successful endoscopic resection of giant ureterocele presenting
with complete urinary retention.
Observation
A 38-Year-old male patient presented to the emergency department with severe lower
abdominal pain and urine retention. foley’s catheter inserted permitted the evacuation of
more than 900cc of urine. Laboratory investigations were normal. Ultrasound of abdomen
and pelvis revealed a huge cystic intravesical lesion obstructing the internal urethral orifice
with left mild hydronephrosis (figure 1). The patient underwent endoscopic resection of the
ureterocele and DJ stent insertion (figure 2,3). The postoperative course was uneventful. The
outpatient follow up revealed no urinary symptoms.
Figure1: left ureterocele presenting as huge intravesical cystic mass.