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川崎病即皮肤粘膜淋巴结综合征(Mucocutane-ous Lymph Node Syudrone,简称MCLS或MLNS)。1961年由川崎发现,1967年首次报告并命名为“急性热性皮肤粘膜淋巴结综合征”(ACute febrile.Mucocutaneous Lymph Node Syndrone)。主要临床特点是持续性发热、皮肤粘膜炎症反应及颈淋巴结肿大,80％的发病年龄<4岁(1)。国内有报告新生儿发病者(2、3)。男:女=1.5:1,四季可发病,国内报道夏秋多见,无区域性.MCLS多发生在日本的婴幼儿,至1982年已发现47000例(4).本病世
Kawasaki disease is Mucocutane-ous Lymph Node Syudrone (MCLS or MLNS for short). It was discovered by Kawasaki in 1961 and first reported in 1967 and named “ACute febrile. Mucocutaneous Lymph Node Syndrone.” The main clinical features are persistent fever, mucocutaneous inflammatory reaction and cervical lymph node enlargement, 80% of the onset age <4 years (1). There are reports of neonatal morbidity (2,3). Male: Female = 1.5: 1, four seasons can be disease, domestic summer and autumn more common, no regional .MCLS occurred in Japan infants and young children, to 1982 has been found in 47000 cases (4)