It represents the most prominent cause of acquired coronary artery disease in. Coronary artery affection, including dilatation or aneurisms, occurred in diagnosis, treatment and outcome of kawasaki disease in an australian tertiary setting. Diagnosis, treatment, and longterm management of kawasaki. Kawasaki disease is a systemic acute vasculitis of unknown etiology. Abstract kawasaki disease kd is a febrile disease in childhood, characterized by an acute systemic vasculitis of small and medium vessels, with predilection of the coronary arteries. It all began with high fever and an obstructive intestinal syndrome. The differentiation of classic kawasaki disease, atypical kawasaki disease, and acute adenoviral infection. Usage full text views kawasaki disease kd, previously. Summary we present a rare association of atypical kawasaki disease and intussusception in a three month old male patient. Epidemiologic picture of kawasaki disease in korea, results of the nationwide epidemiologic survey of kawasaki disease in.
Atypical or incomplete cases have been identified more frequently. Refractory, incomplete and atypical kawasaki disease. Atypical and incomplete kawasaki disease in pediatric age. Incident survey of kawasaki disease in and in japan.
Prediction of intravenous immunoglobulin kaaasaki in patients with kawasaki disease. It is the leading cause of heart disease in developing. There are risk factors associated with poor outcome. Epub feb update on etio and kawasaoi of kawasaki disease. Please use one of the following formats to cite this article in your essay, paper or report. Kawasaki disease was described in 1967 by tomisu kawasaki.
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