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Updated: May 12, 2026

Retzius-Sparing Robot-Assisted Radical Prostatectomy

Retzius-Sparing Robot-Assisted Radical Prostatectomy

Published on: May 19, 2022

Colorectal duplication with prostatorectal fistulae.

Mamta Sengar¹, Chhabi R Gupta, Vishesh Jain

¹Department of Pediatric Surgery, Chacha Nehru Bal Chikitsalaya, Delhi, India 110031.

Journal of Pediatric Surgery

|April 16, 2013

Summary

This study reports a rare case of a child successfully treated for a communicating tubular colonic duplication with prostatorectal fistulae. Early diagnosis and high suspicion are crucial for managing these rare congenital malformations.

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Last Updated: May 12, 2026

Retzius-Sparing Robot-Assisted Radical Prostatectomy

Retzius-Sparing Robot-Assisted Radical Prostatectomy

Published on: May 19, 2022

Area of Science:

Pediatric Surgery
Congenital Malformations
Gastrointestinal Surgery

Background:

Tubular colonic duplications are uncommon congenital anomalies.
Prostatorectal fistulae are exceptionally rare, with few documented cases.
The association between these two conditions is exceedingly rare.

Observation:

A case of an 8-year-old child with a communicating tubular colonic duplication and prostatorectal fistulae is presented.
The patient underwent successful management of this complex condition.
Diagnosis can be challenging due to diverse clinical presentations.

Findings:

Successful surgical management was achieved in a pediatric patient with a rare communicating tubular colonic duplication and prostatorectal fistulae.
This case highlights the successful treatment of an extremely rare congenital anomaly.
The report contributes to the limited literature on this specific association.

Implications:

High clinical suspicion is essential for diagnosing children with isolated congenital recto-urinary fistulas.
Awareness of rare colonic duplications and their potential association with fistulae can improve diagnostic accuracy.
This case underscores the importance of thorough evaluation in pediatric patients presenting with complex anorectal and urinary anomalies.