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川崎病

Kawasaki syndrome.

作者信息

Burns Jane C, Glodé Mary P

机构信息

Division of Allergy, Immunology, and Rheumatology, Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, CA, USA.

出版信息

Lancet. 2004;364(9433):533-44. doi: 10.1016/S0140-6736(04)16814-1.

Abstract

Kawasaki syndrome is an acute, self-limited vasculitis that occurs in children of all ages and presents a challenge for the clinician: the disorder can be difficult to recognise; there is no diagnostic laboratory test; there is an extremely effective therapy; and there is a 25% chance of serious cardiovascular damage if the treatment is not given early in the course of the disease. This review includes discussion of the history of the syndrome, the diagnostic challenges, epidemiology, aetiology, pathology, immunopathogenesis, therapy, genetic influences, and the long-term cardiovascular sequelae.

摘要

川崎病是一种急性自限性血管炎,可发生于各年龄段儿童,给临床医生带来了挑战:该疾病可能难以识别;没有诊断性实验室检查;有极其有效的治疗方法;如果在疾病早期未给予治疗,发生严重心血管损害的几率为25%。本综述包括对该综合征的历史、诊断挑战、流行病学、病因、病理、免疫发病机制、治疗、遗传影响以及长期心血管后遗症的讨论。

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