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[Upper gastrointestinal duplication complicated by perforation in a child]

V P Gavrilyuk1, E V Donskaya2, D A Severinov1

  • 1Kursk State Medical University, Kursk, Russia.

Khirurgiia
|February 21, 2023
PubMed

Insights

This case report details a rare congenital gastrointestinal duplication in a 6-month-old child, involving the stomach, duodenum, and pancreas. Surgical resection was successful, leading to an uneventful recovery.

Area of Science:

  • Gastroenterology
  • Pediatric Surgery
  • Congenital Malformations

Context:

  • Gastrointestinal duplications are rare congenital anomalies.
  • Presentation varies widely based on location and type.
  • Often diagnosed in infancy or early childhood.

Purpose:

  • To report a rare case of extensive gastrointestinal duplication.
  • To highlight the diagnostic and surgical management challenges.
  • To emphasize successful en-bloc resection and recovery.

Summary:

  • A 6-month-old infant presented with symptoms suggestive of intestinal obstruction.
  • Ultrasound revealed an abdominal neoplasm, leading to exploratory laparotomy.
  • A complex duplication of the stomach, duodenum, and pancreas was identified and resected en bloc.

Impact:

  • Demonstrates the successful surgical management of a complex congenital anomaly.
  • Contributes to the literature on rare gastrointestinal duplications.
  • Highlights the importance of prompt diagnosis and intervention in pediatric surgical emergencies.

Keywords:
childrencongenital malformationsduodenum duplicationhollow organ perforationstomach duplicationsurgical treatment

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