Korean J Infect Dis.
2000 Oct;32(5):388-392.
Adult-onset Kawsaki Disease Complicated by Splenic Infarction and
Coronary Aneurysm
Abstract
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Kawasaki disease or mucocutaneous lymph node syndrome is an acute inflammatory illness of
childhood characterized by systemic panvasculitis. It presents with high fever, dramatic
changes of the skin and mucous membranes, and lymphadenopathy. Adult-onset Kawasaki disease
is rare and reports on coronary involvement in adult are even rarer. Herein, we report a case
of adult-onset Kawasaki disease complicated by splenic infarction and development of coronary
aneurysm even despite of treatment with intravenous gamma globulin. A 20-year-old man
presented with fever, erytheatous rash, induration and desquamation of hands and feet,
pulmonary edema and shock due to cardiomyopathy, splenic infarction, bilateral conjunctivitis,
jaundice, and cervical lymphadenopathy. After Kawasaki disease was suspected, intravenous
gamma globulin (2 g/kg once) and aspirin (6 g/day) were administered. On the 30th hospital
day, transesophageal echocardiography showed one coronary aneurysm and coronary angiography
showed three aneurysms. Eight months after the first admission, follow-up coronary angiography
showed normalization of the previous coronary abnormalities.