Clinical Manifestations Vary with Different Age Spectrums in Infants with Kawasaki Disease
Author(s) -
Hao-Chuan Liu,
Chiao-Wei Lo,
Betau Hwang,
Pi-Chang Lee
Publication year - 2012
Publication title -
the scientific world journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.453
H-Index - 93
eISSN - 2356-6140
pISSN - 1537-744X
DOI - 10.1100/2012/210382
Subject(s) - kawasaki disease , medicine , leukocytosis , vasculitis , thrombocytosis , pyuria , etiology , aneurysm , myocardial infarction , gastroenterology , systemic vasculitis , platelet , artery , cardiology , disease , surgery , urinary system
Background . Kawasaki disease (KD) is an acute systemic vasculitis with unknown etiology. The diagnosis of KD depends on clinical manifestations. The prevalence of coronary artery abnormality (CAA) is 11.0% and results in cardiac sequelae, such as myocardial infarction or coronary aneurysm, which are the most serious complications in KD. Methods . We divided KD's children into different age groups: ≤6 months old, 7 months to 1 year old, and >1 year old, respectively. Different parameters were compared in each group. Results . Infants ≤6 months old are less likely to fulfill KD's major diagnostic criteria within 10 days, are prone to develop incomplete KD with the lowest cholesterol level, and have the greatest chance to have CAA and the laboratory features associated with CAA, such as the longest time needed to confirm CA diagnosis, lower hemoglobin level, lower albumin level, and higher platelet count. Infants <1 year old develop higher percentage of leukocytosis and sterile pyuria. But this group has fewer patients with neck lymphadenopathy.
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