摘要
Kawasaki disease(KD) is an acute and self-limited febrile disease characterized by fever, polymorphic rash, bulbar conjunctival congestion, redness of the lip mucosa, unilateral cervical lymphadenopathy, erythema, and edema of the extremities. KD was reported first by Tomisaku Kawasaki, a Japanese scholar, in 1967[1]. Since then, the disease has been reported worldwide, with significant differences observed in its incidence in different regions.
作者
徐泊雯
张清友
杜军保
Isao Shiraishi
金红芳
Bowen Xu;Qingyou Zhang;Junbao Du;Isao Shiraishi;Hongfang Jin(Department of Pediatrics,Peking University First Hospital,Beijing 100034,China;Key Laboratory of Cardiovascular Sciences,the Ministry of Education,Beijing 100191,China;Department of Pediatric Cardiology,National Cerebral and Cardiovascular Center,Osaka 564-8565,Japan)
