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儿童期漏诊的川崎病在成人中表现为心肌梗死。

Missed Kawasaki disease in childhood presenting as myocardial infarction in adults.

作者信息

Bhagwat Ajit, Mukhedkar Sachin, Ekbote Shriganesh, Gordon John B

机构信息

Kamalnayan Bajaj Hospital, Aurangabad, India.

Kamalnayan Bajaj Hospital, Aurangabad, India.

出版信息

Indian Heart J. 2015 Jul-Aug;67(4):385-8. doi: 10.1016/j.ihj.2015.04.014. Epub 2015 May 14.

Abstract

Kawasaki disease (KD) is an acute, self-limited vasculitis that occurs in young children and was first described by Japanese pediatrician Tomisaku Kawasaki in 1967. Although originally thought to be a rare condition, KD has become the most common cause of acquired heart disease in the pediatric population in developed countries. The majority of patients with KD appear to have a benign prognosis, but a subset of patients with coronary artery aneurysms are at risk for ischemic events and require lifelong treatment. In the 4 decades since the initial recognition of KD, the number of patients reaching adulthood has continued to grow. Adult cardiologists will be increasingly involved in the management of these patients. Currently, there are no established guidelines for the evaluation and treatment of adult patients who have had KD. We report 4 most probable cases of KD missed in childhood and presented as acute coronary syndrome in adulthood.

摘要

川崎病(KD)是一种发生于幼儿的急性自限性血管炎,由日本儿科医生川崎富作于1967年首次描述。尽管最初认为这是一种罕见疾病,但川崎病已成为发达国家儿童获得性心脏病的最常见病因。大多数川崎病患者预后似乎良好,但一部分患有冠状动脉瘤的患者有发生缺血性事件的风险,需要终身治疗。自川崎病首次被认识后的40年里,成年患者的数量持续增加。成年心脏病专家将越来越多地参与这些患者的管理。目前,对于曾患川崎病的成年患者的评估和治疗尚无既定指南。我们报告了4例儿童期最可能漏诊的川崎病病例,这些病例在成年后表现为急性冠状动脉综合征。

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