coronary aneurysm/dopamine

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Surgical treatment of giant coronary artery aneurysm secondary to Kawasaki disease.

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OBJECTIVE To investigate the clinical features and surgical management of giant coronary artery aneurysm during end-stage Kawasaki disease. METHODS From May 2006 to October 2007, 5 patients, 2 to 57 years old, presented with giant coronary artery aneurysm and underwent surgical correction. The

Manifestations of Kawasaki disease in New England outbreak of 1980.

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Twenty-five children with Kawasaki disease were studied during the spring of 1980. All had fever, rash, conjunctivitis, and at least two of the remaining three diagnostic criteria. They ranged in age from 7 months to 10 years with an average of 3.2 years. Cardiac manifestations were present in 64%;

Kawasaki disease triggered by parvovirus infection: an atypical case report of two siblings.

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There are reports of the familial occurrence of Kawasaki disease but only a few reports described Kawasaki disease in siblings. However, the familial cases were not simultaneous. In these patients the idea of infective agents as trigger must be

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