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Duplicated Collecting System with Ectopic Vaginal Implantation
Maxim Behaeghe1, Patrick Seynaeve2, Koenraad Verstraete1
1Ghent university, BE.
Journal of the Belgian Society of Radiology
|October 17, 2018
Summary
A rare case of complete ureteral duplication in a 54-year-old woman caused urinary incontinence due to vaginal implantation. This congenital anomaly highlights unusual presentations of urinary tract abnormalities in adults.
Area of Science:
- Urology
- Medical Imaging
- Congenital Anomalies
Background:
- Complete ureteral duplication is a congenital anomaly.
- Vaginal implantation of a ureter is rare, especially in adults.
- Urinary incontinence can stem from complex congenital urinary tract abnormalities.
Observation:
- A 54-year-old woman presented with left-sided complete ureteral duplication.
- The upper ureteral moiety drained into the proximal vagina, forming an ureterocele and causing urinary incontinence.
- The lower moiety had a normal ureteral orifice.
Findings:
- MR colpocystodefecography revealed an ureterocele between the bladder and rectum.
- Computed tomography confirmed duplicated ureters with ectopic vaginal implantation of the upper moiety.
- The anomaly involved proximal renal upper pole and distal vaginal implantation.
Implications:
- This case underscores the importance of considering rare congenital anomalies in adult-onset urinary incontinence.
- Advanced imaging techniques like MR and CT are crucial for diagnosing complex ureteral duplications.
- Understanding such anomalies aids in appropriate management and treatment strategies for affected individuals.
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