Atypical Kawasaki disease with aortic aneurysm.
Atypical Kawasaki disease with aortic aneurysm.
复制标题
非典型川崎病伴主动脉瘤。
作者：
Charles E. Canter;Richard J. Bower;Arnold W. Strauss
Kawasaki disease (mucocutaneous lymph node syndrome), initially described in Japan, is now being seen with increasing frequency in the United States.1 The diagnosis is based on the typical constellation of signs and symptoms.1,2 Mortality is 1% to 2%, and significant morbidity results from aneurysmal formation in midsize arteries, especially the coronary arteries, which may result in rupture or myocardial infarction.
We report an unusual case of Kawasaki disease. The initial febrile illness was an atypical presentation.
A large abdominal aortic aneurysm developed, which subsequently was resected. Seven months after the febrile illness an asymptomatic myocardial infarction secondary to bilateral coronary arterial aneurysms was documented.
