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Utility of post mortem MRI in definition of thrombus in aneurismatic coronary arteries due to incomplete Kawasaki Disease in infants

机译:尸检后MRI在定义因川崎病不完全而导致的婴儿的冠状动脉冠状动脉血栓形成中的作用

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摘要

Kawasaki disease (KD) is an acute, self-limited vasculitis of unknown etiology that primarily affects the coronary artery (CA) and presents in childhood. The characteristic coronary arterial lesion is an aneurysm, which may lead to thrombosis, dilatation, stenosis, and occlusion. Such an aneurysm is typically calcified and generally develops five or more years after the onset of acute KD. It becomes more noticeable after ten years. KD is sometimes difficult to diagnose because of the limited clinical features, especially in infants younger than 6 months old, where the clinical presentations often do not fulfill the diagnostic criteria for KD. We report a case of Incomplete Kawasaki Disease (IKD) causing unexpected death in infants. A seven-month-old male baby, apparently well nourished and without fever or exanthema that was unexpectedly found agonal in his bed by his parents. He died in an emergency room a few hours later in spite of aggressive resuscitation efforts. Postmortem Magnetic Resonance Images were obtained during the autopsy, with evidence of an occlusive thrombus in left and right coronary artery aneurysms. Laboratory findings were consistent with IKD. The crucial role of postmortem imaging is discussed here in order to improve diagnosis tools for preventable events.
机译:川崎病(KD)是一种病因不明的急性自限性血管炎,主要影响冠状动脉(CA)并在儿童时期出现。典型的冠状动脉病变是动脉瘤,可能导致血栓形成,扩张,狭窄和闭塞。这种动脉瘤通常会钙化,通常会在急性KD发作后五年或更长时间发展。十年后变得更加明显。由于临床特征有限,有时难以诊断KD,尤其是在6个月以下的婴儿中,其临床表现通常不符合KD的诊断标准。我们报告一例不完全的川崎病(IKD),导致婴儿意外死亡。一个七个月大的男婴,营养良好,没有发烧或发烧,父母意外在他的床上发现他的病。尽管进行了积极的抢救,他还是在几个小时后死于急诊室。尸检期间获得了尸检后的磁共振图像,证据显示左冠状动脉和右冠状动脉瘤中存在闭塞性血栓。实验室检查结果与IKD一致。为了改进可预防事件的诊断工具,此处讨论了死后成像的关键作用。

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