Congenital Colonic Atresia: 4 Case Reports

Chouikh, Taieb

doi:10.15406/jpnc.2014.01.00018

Cited by 5 publications

(1 citation statement)

References 27 publications

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“…Colonic atresia is a very rare form of intestinal obstruction in neonates, presenting with failure to pass meconium, vomiting and abdominal distension with an incidence rate of 1.8 to 15 per 100 live births in the general population [1]. However, atresia of the colon is known to be the most common determinant leading to intestinal obstruction [2].…”

Section: Introductionmentioning

confidence: 99%

Ileocecal Valve Atresia – A Take on the Aberrant Phenomenon

Panigrahi¹,

Anvekar²,

Lohana³

et al. 2021

Cureus

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Ileocecal valve atresia is the most uncommon yet remarkable form of the atresia found within the gastrointestinal system. We report a case on this rare entity with few cases documented in the literature to date. In our case, a one-day-old full-term male infant who developed the signs of intestinal obstruction was eventually taken for emergency laparotomy. The atretic area found intraoperatively was removed followed by the creation of an anastomosis. The patient recovered well postoperatively and continues regular pediatric follow-ups.

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Section: Introductionmentioning

confidence: 99%

Ileocecal Valve Atresia – A Take on the Aberrant Phenomenon

Panigrahi¹,

Anvekar²,

Lohana³

et al. 2021

Cureus

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Fenestrated Colonic Atresia: A rare presentation

Mahmoud

Omair

Alrashidi

2020

Journal of Pediatric Surgery Case Reports

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The colon membrane as a cause of large bowel obstruction in a child of 11-month old: a case report

Smirnov¹,

Холостова

Война

et al. 2021

Russian Journal of Pediatric Surgery

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Introduction. Colon atresia is a rare form of congenital bowel obstruction. In scientific literature, there are isolated publications devoted to colon atresia, and only some authors discuss the membranous form of atresia.Material and methods. The article describes a rare clinical case of an incomplete colon membrane in an infant. At the age of 11 months, the child developed symptoms of acute intestinal obstruction. Irrigography was performed; Hirschsprung’s disease was suspected. At the first stage, the child was taken a floor-by-floor biopsy of the colon, and an ileostomy was put. Visually, Hirschsprung’s disease seemed to be present; however, histological examination turned aside this diagnosis. Given this, the colon membrane was suspected. Partial resection of the altered part of the sigmoid colon was performed with good clinical effect. Histological examination revealed an incomplete serous-muscular membrane of the colon.Conclusion. Colon atresia is a rare disease that presents a serious problem for diagnosis and treatment. Preoperative morphological verification of the diagnosis is important, even in case when Hirschsprung’s disease seems obvious. Preoperative diagnostics is important because surgical tactics may be considerably different in colon local lesions.

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Congenital Colonic Atresia: 4 Case Reports

Cited by 5 publications

References 27 publications

Ileocecal Valve Atresia – A Take on the Aberrant Phenomenon

Ileocecal Valve Atresia – A Take on the Aberrant Phenomenon

Fenestrated Colonic Atresia: A rare presentation

The colon membrane as a cause of large bowel obstruction in a child of 11-month old: a case report

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