[Pancreatitis: review of our casuistics in the last 10 years]

C Maluenda Carrillo1, F Valverde Moreno, A Bodas Pinedo

  • 1Departamento de Pediatría. Hospital Clínico San Carlos. Madrid. España.

Insights

Childhood pancreatitis is uncommon, primarily affecting teenage girls. Diagnosis relies on elevated amylase and lipase levels, with causes including idiopathic and toxic factors, requiring tailored treatment.

Area of Science:

  • Pediatric Gastroenterology
  • Hepatology and Nutrition
  • Pancreatic Diseases

Background:

  • Pancreatitis in children is a rare condition.
  • Advances in diagnostic imaging improve early detection and treatment of pancreatic diseases.

Observation:

  • A 10-year retrospective study (1990-2000) analyzed pediatric pancreatitis cases.
  • Diagnostic criteria included suggestive symptoms and hyperamylasemia.
  • The study reviewed etiology, diagnostic methods, and management in children aged 0-16.

Findings:

  • The study identified 9 pediatric pancreatitis cases (8 female, 1 male) with a median age of 11.5 years.
  • Elevated amylase (mean 1601 U/l) and lipase (mean 506 U/l) confirmed diagnosis.
  • Etiologies included cholelithiasis, anti-oncological therapy, hypercholesterolemia, and idiopathic causes.
  • Imaging modalities like ultrasonography, CT, ERCP, and MRCP were utilized.
  • Treatment involved supportive care, octreotide, antioxidants, or surgery, with 2 cases developing pancreatic pseudocysts.

Implications:

  • Childhood pancreatitis is rare, predominantly affecting adolescent females.
  • Idiopathic and toxic factors are significant etiological contributors.
  • Diagnosis is established through biochemical markers and advanced imaging.
  • Management strategies are etiology-dependent, ranging from conservative measures to surgical intervention.
Abstract

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