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Ann Trop Paediatr ; 23(3): 187-91, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14567834

ABSTRACT

We describe a 3-year-old boy with Kawasaki disease who, despite therapy with two doses of intravenous immunoglobulin G and high-dose aspirin, developed myocarditis in the 1st week of illness and coronary artery aneurysms in the 2nd week. He required a short course of systemic corticosteroids for remission of the illness. The myocarditis subsided and coronary aneurysms remained static and uncomplicated during 6 weeks of follow-up. The diagnosis and recent trends in management of this not uncommon vasculitic disorder are outlined.


Subject(s)
Immunoglobulin G/therapeutic use , Immunotherapy/methods , Mucocutaneous Lymph Node Syndrome/therapy , Adrenal Cortex Hormones/therapeutic use , Child, Preschool , Coronary Aneurysm/drug therapy , Coronary Aneurysm/etiology , Diagnosis, Differential , Humans , Male , Mucocutaneous Lymph Node Syndrome/complications , Mucocutaneous Lymph Node Syndrome/diagnosis , Myocarditis/drug therapy , Myocarditis/etiology , Treatment Outcome
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