ReviewJournal of Indian Association of Pediatric Surgeons
Congenital Pouch Colon.
Review in Journal of Indian Association of Pediatric Surgeons. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
18 citing papers in PubMed, 34 citations in OpenAlex.
- Distinct genetic variants from the whole-exome sequencing of syndromic anorectal malformations: A cross-sectional study.iScience · 2026Article
- Surgical management of congenital pouch colon in Lebanon: A case report and review of the literature.Radiology case reports · 2024Article
- Management of urinary incontinence in girls with congenital pouch colon.Pediatric surgery international · 2024Article
- Antenatal diagnosis of congenital pouch colon: a case report from the Indian subcontinent with insights into management.BJR case reports · 2024Article
- Congenital Partial Colonic Agenesis in Dogs and Cats: Clinical, Biological, Diagnostic Imaging, Endoscopic and Histopathologic Characterization, a Retrospective Study.Veterinary sciences · 2023Article
- Congenital pouch colon: Case report and literature review.Annals of medicine and surgery (2012) · 2022Article
- Congenital Pouch Colon in a Neonate.Pakistan journal of medical sciences · 2022Article
- Congenital pouch colon in Duhok, outcome and complications: Case series.Annals of medicine and surgery (2012) · 2019Article
- Bowel Imaging in Children: Part 1.Indian journal of pediatrics · 2019Review
- Is Pouch Specific to Colon and Not Ileum?Current pediatric reviews · 2019Review
- Congenital Pouch Colon in Girls: An Algorithm for Preoperative Diagnosis.Journal of Indian Association of Pediatric SurgeonsArticle
- Laparoscopy-assisted Anorectoplasty with Coloplasty for Type-I/II Congenital Pouch Colon.Journal of Indian Association of Pediatric SurgeonsArticle
- Congenital pouch colon: A comparative study between two modalities of management.African journal of paediatric surgery : AJPSArticle
- Type IV Congenital Pouch Colon in Male Children: Anatomical Variations and a Proposed New Subclassification.Journal of Indian Association of Pediatric SurgeonsArticle
- A New Pouch-tapering Technique for the Management of Congenital Pouch Colon.Journal of Indian Association of Pediatric SurgeonsArticle
- Double Threat in a Newborn: High Anorectal Malformation with Pouch Colon and Bilateral Multicystic Dysplastic Kidneys - A Rare Case Report.Journal of Indian Association of Pediatric SurgeonsArticle
- Congenital Pouch Colon in Males: Exploring the Risk of Epididymo-orchitis.Journal of Indian Association of Pediatric SurgeonsArticle
- Abdominoperineal Pull-through with Simultaneous Extravesical Detrussoraphy: An Alternative Surgical Technique for Congenital Pouch Colon with High-grade Vesicoureteric Reflux.Journal of Indian Association of Pediatric SurgeonsArticle
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital pouch colon (CPC) is an unusual abnormality in which a pouch-like dilatation of a shortened colon is associated with an anorectal malformation. It is categorized into four subtypes (Types I-IV) based on the length of normal colon proximal to the colonic pouch. In males, the pouch usually terminates in a colovesical fistula just proximal to the bladder neck. In girls, the terminal fistula opens either into the urethra or in the vestibule, close to the urethral opening. Girls usually have a double vagina with a wide inter-vaginal bridge, a monocornuate uterus on each side, and urinary incontinence due to a widely open bladder neck. Associated major malformations are uncommon with CPC but sometimes, especially in reports from outside India, major abnormalities are present suggesting an early, severe error in embryogenesis. The more severe Types I/II CPC can usually be diagnosed by a large gas shadow or air-fluid level on X-Ray abdomen. For all subtypes of CPC, it is preferable to preserve a segment of the pouch by fashioning a narrow colonic tube for pull-through, the technique known as coloplasty or tubular colorraphy. Girls need additional management of the genitourinary abnormalities. Postoperatively, fecal continence levels are usually poor, especially with Types I/II CPC.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.