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川崎病伴面神经麻痹

Kawasaki disease with facial nerve paralysis.

作者信息

Larralde Margarita, Santos-Muñoz Andrea, Rutiman Ricardo

机构信息

Department of Pediatric Dermatology, Ramos Mejia Hospital, Buenos Aires, Argentina.

出版信息

Pediatr Dermatol. 2003 Nov-Dec;20(6):511-3. doi: 10.1111/j.1525-1470.2003.20612.x.

Abstract

Kawasaki disease (KD) is a multisystem disorder with varying clinical expression. We describe an instance of facial nerve paralysis in a patient with KD. A 5-month-old boy developed fever, irritability, and diarrhea, treated 8 days later with cefaclor and ibuprofen. Three days later a confluent, erythematous and papular rash appeared, his lips were reddened and swollen, and his white blood count and platelet count were 20,900/mm(3) and 558,000/mm(3), respectively. He was admitted to the hospital with a diagnosis of KD, and an echocardiogram showed a right coronary aneurysm. The patient then developed an acute, right-sided, facial nerve peripheral paralysis that resolved over the next 6 weeks. He was treated with intravenous immune globulin (IVIG) 2 g/kg and aspirin 100 mg/kg/day with improvement of signs and symptoms. This report documents facial nerve paralysis as an uncommon complication of KD and points out that it may be a marker of increased risk of cardiovascular disease in this disorder.

摘要

川崎病(KD)是一种临床表现多样的多系统疾病。我们描述了一例KD患者出现面神经麻痹的病例。一名5个月大的男孩出现发热、烦躁和腹泻,8天后接受头孢克洛和布洛芬治疗。三天后出现融合性红斑丘疹皮疹,嘴唇红肿,白细胞计数和血小板计数分别为20,900/mm³和558,000/mm³。他因诊断为KD入院,超声心动图显示右冠状动脉瘤。随后患者出现急性右侧面神经周围性麻痹,在接下来的6周内逐渐缓解。他接受了2 g/kg静脉注射免疫球蛋白(IVIG)和100 mg/kg/天阿司匹林治疗,症状体征有所改善。本报告记录了面神经麻痹是KD一种罕见的并发症,并指出它可能是该疾病中心血管疾病风险增加的一个标志。

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