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Urethrorectal fistula repair in children: urologic perspective
Tamer E Helmy1, Osama M Sarhan, Mohamed E Dawaba
1Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Insights
Urethrorectal fistulas are rare, complex conditions in children, often requiring surgical repair. Perineal repair, though challenging, can be successful with meticulous technique.
Area of Science:
- Pediatric Surgery
- Urology
- Gastroenterology
Background:
- Urethrorectal fistulas are rare congenital or acquired anomalies.
- Management is complex due to the rarity and varied etiologies.
Purpose of the Study:
- To report experience in managing pediatric urethrorectal fistulas.
- To emphasize the complexity and successful management strategies for this condition.
Main Methods:
- Retrospective review of 5 pediatric cases (1997-2007).
- Analysis of patient demographics, fistula type, surgical approach, and outcomes.
Main Results:
- Mean age 6.8 years; one congenital, four acquired fistulas.
- Presentations included urinary and fecal diversion; perineal approach used in 4/5 cases.
- One patient required optical internal urethrotomy for anastomotic stricture.
Conclusions:
- Urethrorectal fistula is a rare complication, congenital or iatrogenic.
- Perineal repair demands meticulous dissection, vascularized flaps, and offers potential success.
Objectives:
We report our experience in the management of urethrorectal fistulae in children with emphasis on the complexity of this rare disease.
Patients And Methods:
A retrospective review was performed in cases that underwent repair of urethrorectal fistula at our center between 1997 and 2007. Records were reviewed for age, history, presentation, radiologic data, operative data, and condition at last follow-up.
Results:
Five children were managed for urethrorectal fistula. Their mean age was 6.8 years (range, 2 months-12 years). One case had congenital urethrorectal fistula and four had acquired fistulas including two after abdomino-perineal pull through for imperforate anus, one case post perineal urethroplasty, and another post repair of posttraumatic rectal tear. All patients presented with history of passing urine both through the rectum and the urethral meatus. We have three urinary diverted cases: one case in whom urinary and fecal diversions were performed and the remaining case was operated without diversion. Perineal approach was adopted in four procedures and abdomino-perineal approach in one. One patient required optical internal urethrotomy for anastomotic stricture at 6 months follow-up.
Conclusions:
Urethrorectal fistula is a rare complication whether congenital or iatrogenic. Perineal repair is challenging, necessities meticulous dissection, adequate vascularity of the edges, and interposition of vascularized flaps and is potentially successful.
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