Ureteral triplication with a contralateral duplication and ureterocele: a case report.
Fayza Alhajri1, Ammar Al-Jumah, Sara Al-Mutawa
1Department of Clinical Radiology, Mubarak Al-Kabeer Hospital Jaberiya Kuwait. faabd2000@yahoo.com
Cases Journal
|October 16, 2009
Summary
A rare case of left ureteral triplication (Smith type 2) with contralateral duplication and ureterocele in a 10-year-old boy highlights the importance of early diagnosis for preventing kidney damage.
Area of Science:
- Pediatric Urology
- Congenital Anomalies
- Radiology
Background:
- Ureteral anomalies are uncommon congenital abnormalities affecting the urinary tract.
- Nocturnal enuresis can be a symptom of underlying urological conditions.
- Ureteral triplication, particularly Smith type 2, is exceptionally rare.
Observation:
- A 10-year-old male presented with persistent nocturnal enuresis.
- Radiological imaging identified a left ureteral triplication (Smith type 2).
- Contralateral ureteral duplication and a ureterocele were also noted.
Findings:
- The patient exhibited an extremely rare combination of ureteral anomalies.
- The specific presentation involved a triplicated left ureter and a duplicated right ureter with a ureterocele.
- This complex anomaly was diagnosed via radiological workup.
Implications:
- Early diagnosis of such rare congenital anomalies is crucial.
- Prompt management can prevent serious complications like recurrent urinary tract infections and renal damage.
- This case underscores the need for thorough investigation in pediatric patients with persistent enuresis.
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