A Case Report of Childhood Recurrent Autoimmune Pancreatitis: A Rare Emerging Entity

Mohammed Y Hasosah1, Lojain Masawa2, Ajwan Jan2

  • 1Assistant Professor, Department of Pediatric Gastroenterology, King Saud Bin Abdulaziz University for Health Sciences, National Guard Hospital , Jeddah, Saudi Arabia .

Insights

Autoimmune pancreatitis (AIP), a rare condition in children, presents with abdominal pain. Early diagnosis and corticosteroid treatment are crucial for managing this IgG4-related disease.

Area of Science:

  • Pediatric Gastroenterology
  • Immunology
  • Pancreatic Diseases

Background:

  • Autoimmune pancreatitis (AIP) is an uncommon pancreatic disorder with unknown etiology in children.
  • Recurrent pancreatitis in pediatric patients requires thorough differential diagnosis.

Observation:

  • A 10-year-old girl presented with recurrent abdominal pain.
  • Diagnostic workup revealed elevated pancreatic enzymes, elevated IgG4 levels, and characteristic imaging findings consistent with AIP.

Findings:

  • The patient demonstrated a positive response to corticosteroid therapy.
  • Diagnosis of AIP was confirmed through a combination of clinical, serological, and imaging data.

Implications:

  • Autoimmune pancreatitis should be considered in the differential diagnosis of pediatric recurrent pancreatitis.
  • Timely and accurate diagnosis of AIP can prevent disease progression and avoid unnecessary surgical interventions.

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