川崎病的最新进展

Tomo Matsubara
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引用次数: 0

摘要

川崎病(Kawasaki disease, KD)在1967年的《日本变态反应学杂志》上被报道为一种新疾病。根据临床症状诊断KD的指南于2019年进行了修订,第六次修订的目的是重点关注KD的及时诊断,而不是延误治疗静脉免疫球蛋白耐药急性KD的治疗很重要KD的发病机制是遗传易感儿童全身性炎症引起的血管炎在最近和正在进行的冠状病毒病2019 (COVID-2019)大流行期间,在欧洲和美国报告了表现出与KD相似特征的儿科重症病例,需要进一步的研究来阐明COVID-19在KD发病机制中的作用
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kawasaki disease -up to date-
Abstract Kawasaki disease (KD) was reported as a novel disease in The Japanese Journal of Allergology in 1967 Although many causative pathogens have been proposed, the cause of KD remains unknown The guidelines for the diagnosis of KD using clinical symptoms were revised in 2019 The purpose of this 6th revision is to focus on the prompt diagnosis for KD for not delaying treatment The treatment for intravenous immunoglobulin-resistant acute KD is important The pathogenesis of KD is vasculitis caused by systemic inflammation in genetically susceptible children During the recent and ongoing coronavirus disease 2019 (COVID-2019) pandemic, the pediatric severe cases showing features similar to KD were reported in Europe and US Further studies will be needed to clarify the involvement of COVID-19 in the pathogenesis of KD
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