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作 者:Takashi Furuta Hiroki Yasudo Seigo Okada Yuji Ohnishi Akiko Kawakami-Miyake Yasuo Suzuki Shouichi Ohga Shunji Hasegawa
机构地区:[1]Department of Pediatrics,Yamaguchi University Graduate School of Medicine,1-1-1 Minamikogushi,Ube,Yamaguchi,755-8505,Japan [2]Department of Pediatrics,Graduate School of Medical Sciences,Kyushu University,3-1-1 Maidashi,Higashi-ku,Fukuoka,812-8582,Japan
出 处:《World Journal of Pediatrics》2022年第11期781-785,共5页世界儿科杂志(英文版)
基 金:This work was supported in part by Japan Society for the Promotion of Science(JSPS)KAKENHI[Nos.16K19647(SY),19K08323(SH),and 21K15906(OS)]from the Ministry of Education,Culture,Sports,Science and Technology.
摘 要:Kawasaki disease(KD)is an acute febrile ilness characterized by systemic vasculitis affecting the small-and mediumsized arteries in children [1,2].One of the most critical complications of KD is the development of coronary artery lesions(CALs)approximately after 12 days of ilness,which may lead to myocardial infarction[3].High-dose intravenous immunoglobulin(IVIG)and oral administration of aspirin have been established as the first-line therapy for KD[4,5].
关 键 词:INTRAVENOUS acute IMMUNOGLOBULIN
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