Abstract
Kawasaki disease (KD) is an acute vasculitis leading to systemic inflammatory manifestations. The classic clinical criteria of KD include fever persisting at least 5 days and at least four out of five features (extremity changes, polymorphous exanthem, conjunctival injection, oral/lip changes, and cervical lymphadenopathy). Patients with KD will almost always have an elevated C-reactive protein and/or erythrocyte sedimentation rate. KD is treated with immunoglobulin and aspirin with the goal of preventing the development of coronary artery aneurysms.
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Ishimine, P., Kanegaye, J.T. (2018). Kawasaki Disease. In: Rose, E. (eds) Life-Threatening Rashes. Springer, Cham. https://doi.org/10.1007/978-3-319-75623-3_7
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DOI: https://doi.org/10.1007/978-3-319-75623-3_7
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