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Incomplete and Atypical Kawasaki Disease: A Clinicopathologic Paradox at High Risk of Sudden and Unexpected Infant Death

机译:不完全和非典型川崎病:婴儿猝死和意外死亡的高风险的临床病理悖论

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摘要

Incomplete Kawasaki disease (IKD) and atypical Kawasaki disease (AKD) represent rare conditions. Two cases of unexpected or sudden infant death are reported. The diagnosis for a 3-month-old girl was determined by echocardiography, and the child unexpectedly died despite appropriate treatment, whereas autopsy determined the diagnosis of AKD for a 4-month-old boy. In both patients, giant coronary artery aneurysms with thrombosis and vasculitis, myocarditis, and coagulative necrosis were shown at autopsy. These rare forms of IKD and AKD carry a poor prognosis and represent a paradox between the severe cardiovascular damage and the clinical presentation that mimics common and usually self-limiting exanthematic infectious disease in infancy.
机译:不完整的川崎病(IKD)和非典型川崎病(AKD)代表罕见病。据报道有两例婴儿意外或突然死亡。通过超声心动图确定了一个3个月大女孩的诊断,尽管进行了适当的治疗,该孩子却意外死亡,而尸检确定了一个4个月大男孩的AKD诊断。在这两名患者中,尸检均显示巨大的冠状动脉瘤伴有血栓形成和血管炎,心肌炎和凝血坏死。这些罕见的IKD和AKD形式预后较差,并且代表了严重的心血管损害与模仿婴儿期常见且通常是自限性的放血性传染病的临床表现之间的矛盾。

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