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Acute abdomen secondary to complete tubular colonic duplication

Javier Castejón-Casado1, Ma Muñoz Miguelsanz1, E Moreno Diaz1

  • 1Division of Pediatric Surgery, Hospital "Virgen de las Nieves", Granada, Spain.

Journal of Indian Association of Pediatric Surgeons
|September 9, 2014
PubMed

Insights

A rare case of complete large intestine duplication in an infant caused acute abdomen and metabolic issues. Surgical treatment requires careful consideration of the unique anatomical challenges.

Area of Science:

  • Pediatric Surgery
  • Gastrointestinal Malformations
  • Congenital Anomalies

Background:

  • Congenital anomalies of the gastrointestinal tract are diverse.
  • Intestinal duplications are rare malformations with varied presentations.
  • Complete duplication of the large intestine is exceptionally uncommon.

Observation:

  • A 6-month-old infant presented with symptoms of acute abdomen.
  • The infant also exhibited severe metabolic disturbances.
  • Diagnostic imaging revealed a complete duplication of the large intestine.

Findings:

  • The duplication presented unique morphological characteristics.
  • Pathogenesis of this rare anomaly was explored.
  • Surgical intervention posed significant challenges due to the anomaly's extent.

Implications:

  • This case highlights the importance of considering rare congenital anomalies in infants with acute abdomen.
  • Understanding the morphology and pathogenesis aids in diagnosis and surgical planning.
  • Peculiarities in surgical treatment for complete large intestine duplication offer valuable insights for pediatric surgeons.

Keywords:
Acute abdomenascitescolonduplication

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