Affiliations 

  • 1 Universiti Teknologi MARA (UiTM), Faculty of Medicine, Sungai Buloh Campus, Selangor, Malaysia. azizahdublin@gmail.com
  • 2 Hospital Selayang, Department of Paediatrics, Selangor, Malaysia
  • 3 Hospital Kuala Lumpur, Institute of Paediatrics, Department of Paediatrics, Kuala Lumpur, Malaysia
Med J Malaysia, 2018 08;73(4):257-259.
PMID: 30121692 MyJurnal

Abstract

Kawasaki disease (KD) is an acute systemic vasculitis usually affecting children <5 years old. We report a 44-dayold baby who had persistent fever despite being on antibiotics for presumed sepsis. Erythema of Bacillus Calmette-Guerin (BCG) scar and thrombocytosis were noted on day-2 of illness. Diagnosis of incomplete KD was made on the 10th day of illness. Her fever resolved with intravenous immunoglobulin, but echocardiogram revealed coronary artery aneurysm. High index of suspicion is required to diagnose KD in infants ≤3 months since it is rare and commonly presents with incomplete clinical features. The presence of unexplained fever for ≥5 days with erythema of BCG scar or thrombocytosis in infants should alert the clinicians of KD.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.