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病例报告:川崎病患儿的下肢肌肉无力

Case Report: Lower Limb Muscle Weakness in a Child With Kawasaki Disease.

作者信息

Huang Lilin, Peng Shumei, Li Jing, Xie Danyu

机构信息

Department of Pediatrics, Guangdong Women and Children Hospital, Guangzhou, China.

出版信息

Front Pediatr. 2022 Jun 21;10:893568. doi: 10.3389/fped.2022.893568. eCollection 2022.

Abstract

Kawasaki disease (KD) is a systemic vasculitis that may impact multiple organ systems in children. Myositis is an unusual presentation of KD that presents with muscle weakness. To date, a few pediatric patients with KD and myositis have been reported. Diffuse muscle weakness involving the 4 limbs was the most common presentation in these children. However, isolated lower limb involvement was rarely reported before. Here, we report lower limb muscle weakness in an 18-month-old child with KD. He presented with fever, rash, conjunctival injection, peeling over fingers and toes, and progressive muscle weakness of the lower limbs. Muscle enzymes were normal, but electromyography indicated myositis. The symptom of fever was relieved quickly by intravenous immunoglobulin and aspirin, which were ineffective for myositis. However, lower limb muscle weakness fully recovered 5 days after prednisolone treatment. This rare case might add value to the growing literature exploring the association of KD with myositis.

摘要

川崎病(KD)是一种可能影响儿童多个器官系统的全身性血管炎。肌炎是KD的一种不常见表现,表现为肌肉无力。迄今为止,仅有少数KD合并肌炎的儿科患者被报道。这些儿童中最常见的表现是累及四肢的弥漫性肌肉无力。然而,此前孤立的下肢受累情况鲜有报道。在此,我们报告一名18个月大患KD儿童出现下肢肌肉无力的病例。他表现为发热、皮疹、结膜充血、手指和脚趾脱皮以及下肢进行性肌肉无力。肌肉酶正常,但肌电图显示为肌炎。静脉注射免疫球蛋白和阿司匹林可迅速缓解发热症状,但对肌炎无效。然而,泼尼松龙治疗5天后下肢肌肉无力完全恢复。这个罕见病例可能会为不断增多的探索KD与肌炎关联的文献增添价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8078/9253666/585522015fb3/fped-10-893568-g001.jpg

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