A rare case of mesenteric heterotopic pancreas presenting as an inflammatory mass

Yaying Eileen Xu1, Rasika Hendahewa1

  • 1General Surgical Department, Caboolture Hospital, Caboolture, Queensland 4510, Australia.

Insights

This case report details a rare instance of mesenteric heterotopic pancreas (MHP) in a 7-year-old boy, presenting as an inflammatory mass. Early recognition of MHP is crucial for effective pediatric abdominal pain management.

Area of Science:

  • Gastroenterology
  • Pediatric Surgery
  • Pathology

Background:

  • Heterotopic pancreas (HP) is a rare congenital anomaly where pancreatic tissue is found outside its normal location.
  • Mesenteric heterotopic pancreas (MHP) is an exceptionally rare form of HP, with limited pediatric case reports.
  • HP is often asymptomatic, discovered incidentally during autopsy or abdominal surgery, typically in the upper GI tract.

Observation:

  • A 7-year-old African boy presented with symptoms mimicking appendicitis.
  • Intraoperative findings revealed a necrotic nodular mass within the jejunal mesentery.
  • The mass necessitated a segmental small bowel resection.

Findings:

  • Histological examination confirmed the diagnosis of mesenteric heterotopic pancreas.
  • The resected pancreatic tissue was morphologically normal.
  • This represents one of the youngest reported cases of MHP.

Implications:

  • Pre-operative diagnosis of MHP in children is challenging.
  • Increased clinical awareness of MHP is vital for pediatric patients presenting with abdominal pain and inflammatory masses.
  • Prompt diagnosis and management can improve patient outcomes.

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