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不完全性和非典型川崎病:一种具有婴儿猝死高风险的临床病理矛盾现象。

Incomplete and atypical Kawasaki disease: a clinicopathologic paradox at high risk of sudden and unexpected infant death.

作者信息

Pucci Angela, Martino Silvana, Tibaldi Maria, Bartoloni Giovanni

机构信息

Department of Pathology, Regina Margherita Pediatric Hospital, Turin, Italy.

出版信息

Pediatr Cardiol. 2012 Jun;33(5):802-5. doi: 10.1007/s00246-012-0186-y. Epub 2012 Feb 10.

Abstract

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.

摘要

不完全川崎病(IKD)和非典型川崎病(AKD)均为罕见病症。本文报告了两例意外或突然婴儿死亡病例。一名3个月大女孩的诊断通过超声心动图确定,尽管接受了适当治疗,该患儿仍意外死亡,而尸检确定一名4个月大男孩患有AKD。两名患者尸检均显示有巨大冠状动脉瘤伴血栓形成和血管炎、心肌炎以及凝固性坏死。这些罕见形式的IKD和AKD预后不良,并且在严重心血管损害与模仿婴儿期常见且通常为自限性发疹性传染病的临床表现之间存在矛盾。

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