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Acute Jaundice in a Six-year-old: An Unusual Presentation of Atypical Kawasaki Disease
William Bylund1, Gregory J Zarow2,3, Daphne Morrison Ponce4
1Naval Hospital Okinawa, Department of Emergency Medicine, Okinawa, Japan.
Insights
This case highlights incomplete Kawasaki disease (KD) in a child who presented without fever. Early recognition and treatment with intravenous immunoglobulin prevented severe cardiac complications, emphasizing the importance of considering KD even with atypical symptoms.
Area of Science:
- Pediatrics
- Rheumatology
- Immunology
Background:
- Kawasaki disease (KD) is a critical childhood vasculitis associated with significant morbidity and mortality.
- Early diagnosis and treatment are essential to prevent severe sequelae, particularly cardiac complications.
Observation:
- A six-year-old male presented with jaundice and direct hyperbilirubinemia, initially afebrile in the emergency department.
- The patient subsequently developed fever, rash, and desquamation, meeting criteria for incomplete KD.
Findings:
- The case demonstrates an unusual presentation of incomplete Kawasaki disease with hyperbilirubinemia in a child who was initially afebrile.
- Treatment with intravenous immunoglobulin successfully averted cardiac involvement.
Implications:
- This case underscores the need for heightened clinical suspicion for Kawasaki disease, even in the absence of typical fever at presentation.
- Recognizing atypical presentations of incomplete KD is crucial for timely intervention and improved patient outcomes.
Abstract:
Kawasaki disease (KD) is a rare vasculitis of childhood that is critical to recognize and treat due to associated morbidity and mortality. A six-year-old male presented to our emergency department (ED) afebrile but with reported recent fevers. Exam revealed jaundice and erythematous tongue with papules, and laboratory studies indicated a direct hyperbilirubinemia. Admitted for evaluation, he developed continuous fever, increasing maculopapular rash, and subsequent desquamation of hands and feet. He ultimately met criteria for incomplete KD, was treated with intravenous immunoglobulin, and avoided cardiac complications. This presentation of incomplete KD with hyperbilirubinemia is rare because the patient was afebrile at ED presentation.
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