Reye's syndrome developing in an infant on treatment of Kawasaki syndrome

Chih-Ming Wei1, Huey-Ling Chen, Ping-Ing Lee

  • 1Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.

Insights

High-dose aspirin therapy for Kawasaki syndrome in an infant led to Reye's syndrome. Early diagnosis and liver biopsy confirmed the condition, with complete recovery and no recurrence.

Area of Science:

  • Pediatrics
  • Toxicology
  • Gastroenterology

Background:

  • Kawasaki syndrome is treated with high-dose aspirin to prevent coronary artery complications.
  • Standard treatment protocols involve escalating aspirin doses followed by maintenance therapy.

Observation:

  • A 10-month-old infant diagnosed with Kawasaki syndrome received high-dose aspirin therapy.
  • The infant developed acute symptoms including lethargy, hepatomegaly, coagulopathy, and hyperammonemia.

Findings:

  • Liver biopsy findings were consistent with Reye's syndrome, a rare but serious condition.
  • The infant's symptoms resolved completely with supportive care, and no recurrence was observed.

Implications:

  • This case highlights a potential adverse effect of high-dose aspirin in infants with Kawasaki syndrome.
  • Clinicians should maintain a high index of suspicion for Reye's syndrome in infants presenting with similar symptoms during aspirin therapy.