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Brown bowel syndrome: a late complication of intestinal atresia

H C Ward1, J Leake, P J Milla

  • 1Hospital for Sick Children, London, England.

Insights

Children with prior jejunal atresia repair developed dilated small intestine, presenting as "brown bowel" due to muscle changes and vitamin E deficiency. Treatment involved surgical correction and nutritional support.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Nutritional Science

Background:

  • Jejunal atresia is a congenital condition requiring neonatal surgical correction.
  • Post-correction complications can include long-term small intestine issues.
  • Nutritional deficiencies, particularly vitamin E, can arise from gastrointestinal malabsorption.

Observation:

  • Two pediatric patients, previously treated for jejunal atresia, presented with massive proximal small intestine dilation.
  • This dilation was characterized by circular muscular hypertrophy and lipofuscin deposition, leading to a "brown bowel" appearance.
  • The condition was clinically associated with significant malnutrition and documented vitamin E deficiency.

Findings:

  • The "brown bowel" finding in these cases is linked to muscular changes and pigment accumulation in the dilated jejunum.
  • Malnutrition and vitamin E deficiency were key comorbidities, suggesting impaired nutrient absorption.
  • Surgical intervention included limited resection, extensive tapering of the dilated segment, and end-to-end reanastomosis.

Implications:

  • This case highlights a rare but serious long-term complication of jejunal atresia repair.
  • Early recognition and management of "brown bowel" syndrome are crucial for preventing malnutrition and improving outcomes.
  • Long-term nutritional support and vitamin E supplementation are essential components of patient care.

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