Related Experiment Video
Updated: Mar 26, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases
Praveen Jhanwar1, Nand Kishor Shinde1, Jigar N Patel1
1Department of Pediatric Surgery, Lady Harding Medical College and Kalawati Saran Children's Hospital, New Delhi-110001.
Insights
This study details two cases of cloaca and pseudoexstrophy in newborn girls, highlighting a rare congenital pouch colon (CPC) type II with associated genital anomalies. Initial management involved diverting proximal ileostomy for these complex congenital conditions.
Area of Science:
- Pediatric Surgery
- Congenital Abnormalities
- Genitourinary Development
Background:
- Cloaca and pseudoexstrophy are rare congenital malformations presenting complex challenges in neonates.
- Congenital pouch colon (CPC) is an uncommon form of intestinal malrotation, often associated with other anomalies.
- The combination of cloaca, pseudoexstrophy, and CPC type II is exceptionally rare, necessitating detailed case reporting.
Abstract:
This report describes two newborn girls with single perineal opening (cloaca), and pseudoexstrophy in the form of divergent pubic bones and rectus muscles, and a low-set umbilicus. Both patients had a type II congenital pouch colon (CPC) with one hemiuterus and vagina on each side in the pelvis. In one patient, a Meckel's diverticulum was present 5 cm from the ileocecal junction. In both girls, a diverting proximal ileostomy was the initial surgery.
Related Concept Videos
Inflammatory Bowel Disease V: Surgical Management
Here are some common surgical interventions for IBD:
Pleiotropy
Assessment of the Rectum and Anus
Rectal Inspection
Begin by inspecting the perianal and anal areas for color, texture, rashes,...

