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Cecal duplication causing a disappearing abdominal mass in an infant

J L Martins1, E K Cury, A S Petrilli

  • 1Section of Pediatric Surgery, Department of Surgery, Federal University of São Paulo, Paulista School of Medicine, São Paulo, SP, Brazil.

Insights

A rare cystic duplication of the cecum caused an intestinal intussusception in a 2-year-old girl. Surgical intervention successfully resolved the condition, highlighting diagnostic challenges in pediatric gastrointestinal malformations.

Area of Science:

  • Pediatric Surgery
  • Gastrointestinal Malformations
  • Congenital Abnormalities

Background:

  • Alimentary tract duplications are uncommon congenital anomalies.
  • Intestinal intussusception can be a complication of these duplications.

Observation:

  • A 2-year-old girl presented with symptoms suggestive of intestinal intussusception.
  • Initial ultrasonography revealed a transient abdominal mass, complicating diagnosis.
  • The intussusception was ultimately diagnosed and confirmed during surgical exploration.

Findings:

  • A cystic duplication of the cecum, measuring 4 x 3 cm, was identified as the cause of intussusception.
  • The duplication exhibited a granular mucous layer and an ulcerated interior with inflammation.
  • Surgical management involved reduction of intussusception and right hemicolectomy with ileocolic anastomosis.

Implications:

  • This case underscores the diagnostic difficulties associated with rare gastrointestinal duplications.
  • Prompt surgical intervention is crucial for managing intussusception secondary to cecal duplication.
  • Successful surgical outcomes are achievable even with complex presentations.

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