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Sudden cardiac death resulting from acute coronary artery aneurysm occlusion: successful resuscitation and treatment of an adolescent boy with previously unrecognized Kawasaki disease.

机译:由急性冠状动脉瘤闭塞导致的心源性猝死:成功复苏和治疗患有先前未发现的川崎病的青春期男孩。

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摘要

Kawasaki disease (mucocutaneous lymph node syndrome) is an inflammatory vasculitis of unknown etiology1'2 that is the most common cause of acquired coronary artery disease in children between 6 months and 5 years of age.3 Kawasaki disease is also the leading cause of acquired pediatric heart disease in the United States, exceeding rheumatic heart disease.4 Originally described5 and most common in Japan, Kawasaki disease is more prevalent in children of Asian or Pacific Island extraction compared with those of African-American or White decent.6 The disease affects boys more frequently than girls, occurs before the age of 5 years in more than three-quarters of affected children, and carries an overall mortality rate of approximately 0.17%.
机译:川崎病(粘膜皮肤淋巴结综合征)是一种病因不明的炎性血管炎1'2,是6个月至5岁儿童中获得性冠状动脉疾病的最常见原因。3川崎病也是获得性儿科的主要原因在美国,心脏病超过风湿性心脏病。4最初描述5,在日本最常见,与非裔美国人或白人一样,川崎病在亚洲或太平洋岛屿抽取儿童中更为普遍。6该疾病影响男孩在女孩中,四分之三以上的患病率比女孩高,发生在5岁之前,总死亡率约为0.17%。

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