Kawasaki Disease Shock Syndrome: A Challenging Diagnosis

Raquel Penteado, A. Simões, A. Palma, Joana V Andrade, T. Dionísio
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Abstract

The authors present a clinical report of a previously healthy 4-year-old girl, admitted to a pediatric intensive care unit (PICU) presenting with a fluid-refractory shock. She was initially admitted in the pediatric emergency department with a history of fever and petechial rash and an initial diagnosis of invasive meningococcal disease was placed. During the PICU stay, acute myocarditis with episodes of supraventricular tachycardia and lateral and inferior wall myocardial ischemia, ileitis and serositis were noted. At 14th day of stay, she developed peeling on the hands and feet and, aneurysmatic ectasia of the coronary arteries were visualized in transthoracic echocardiography, allowing the diagnosis of Kawasaki disease shock syndrome (KDSS). The child improved after empirical treatment with antibiotics, intravenous immunoglobulin and corticosteroid therapy. She was started on antiplatelet therapy due to changes in the coronary arteries. Early recognition of KDSS can be challenging; however, a delayed diagnosis increases the risk of coronary changes and a fatal outcome. Int J Clin Pediatr. 2021;10(1):10-17 doi: https://doi.org/10.14740/ijcp425
川崎病休克综合征:一个具有挑战性的诊断
作者提出了一个先前健康的4岁女孩的临床报告,入院儿科重症监护病房(PICU)表现为液体难治性休克。她最初因发热和点疹病史住进儿科急诊科,初步诊断为侵袭性脑膜炎球菌病。在PICU期间,急性心肌炎伴室上性心动过速发作、侧壁和下壁心肌缺血、回肠炎和浆膜炎被注意到。住院第14天,患者出现手脚脱皮,经胸超声心动图显示冠状动脉动脉瘤性扩张,诊断为川崎病休克综合征(KDSS)。经抗生素、静脉注射免疫球蛋白和皮质类固醇治疗后,患儿病情好转。由于冠状动脉病变,她开始接受抗血小板治疗。早期识别KDSS可能具有挑战性;然而,延迟诊断会增加冠状动脉病变和致命后果的风险。国际儿科临床杂志。2021;10(1):10-17 doi: https://doi.org/10.14740/ijcp425
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