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Kawasaki disease shock syndrome: a rare and severe complication of Kawasaki disease

机译:川崎疾病休克综合征:川崎病的罕见和严重并发症

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Kawasaki disease is an acute systemic vasculitis that occurs most commonly in young children. It affects medium-sized muscular arteries and the coronary arteries are the predominant site of involvement. Morbidity and mortality is generally due to coronary artery aneurysms that develop during the chronic phase. Although it is well known that Kawasaki disease can cause myocarditis, tachycardia and heart failure during acute stage, Kawasaki disease shock syndrome has been recently described. It is characterized by hypotension, signs and symptoms of poor perfusion and a shock-like state. Herein we describe two cases of Kawasaki disease shock syndrome that were treated in the pediatric intensive care unit and followed a course without morbidity or mortality.
机译:川崎病是一种急性的全身血管炎,最常见于幼儿。 它影响中型肌动脉,冠状动脉是参与的主要遗址。 发病率和死亡率通常是由于在慢性阶段产生的冠状动脉动脉瘤。 虽然众所周知,川崎病会导致心肌炎,心动过速和心力衰竭在急性阶段,最近已经描述了川崎病休克综合征。 它的特征在于灌注不良的低血压,迹象和症状和休克状状态。 在此,我们描述了在儿科重症监护病房中治疗的川崎病休克综合征的两种情况,然后在没有发病率或死亡率的情况下进行课程。

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