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疫苗接种可能引发免疫介导性坏死性肌病。

Vaccination as a possible trigger for immune-mediated necrotising myopathy.

机构信息

Laboratory of Neuromuscular Disease, Department of Neurosciences, Centro Universitário FMABC, Santo Andre, Brazil.

Centro Universitário FMABC, Santo Andre, SP, Brazil.

出版信息

BMJ Case Rep. 2021 May 11;14(5):e242095. doi: 10.1136/bcr-2021-242095.

Abstract

Immune-mediated necrotising myopathy is a rare autoimmune myopathy characterised by severe progressive muscle weakness, elevated levels of creatine kinase (CK), and necrosis with minimal inflammatory cell infiltration on muscle biopsy. We report a case of a previously healthy 42-year-old woman who presented with progressive muscle weakness 2 weeks after immunisation for yellow fever, tetanus/diphtheria and hepatitis B. Her symptoms started from the lower limbs and progressed to the upper limbs and cervical region associated with dysphagia, making her wheelchair bound. Electromyography showed a myopathic pattern, with a CK level of 12.177 U/L (reference value: 26-190 U/L), and biceps brachial muscle biopsy confirmed necrosis and regeneration fibres. The immunoblot test was positive for antisignal recognition particle. She was successfully treated with prednisone (1 mg/kg/day). Although considered safe, vaccines may cause allergic reactions or trigger autoimmune disorders. Currently, a causal relationship between them cannot be established.

摘要

免疫介导性坏死性肌病是一种罕见的自身免疫性肌病,其特征为严重进行性肌无力、肌酸激酶(CK)水平升高,以及肌肉活检时出现最小程度的炎症细胞浸润的坏死。我们报告了一例先前健康的 42 岁女性病例,她在接种黄热病、破伤风/白喉和乙型肝炎疫苗后 2 周出现进行性肌无力。她的症状从下肢开始,进展到上肢和颈部,并伴有吞咽困难,导致她需要坐轮椅。肌电图显示肌病模式,CK 水平为 12.177 U/L(参考值:26-190 U/L),肱二头肌肌活检证实存在坏死和再生纤维。免疫印迹试验抗信号识别颗粒抗体阳性。她接受泼尼松(1 mg/kg/天)治疗后病情得到缓解。尽管疫苗被认为是安全的,但它们可能会引起过敏反应或引发自身免疫性疾病。目前,尚不能确定它们之间存在因果关系。

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本文引用的文献

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Immune-Mediated Necrotizing Myopathy.免疫介导性坏死性肌病。
Curr Rheumatol Rep. 2018 Mar 26;20(4):21. doi: 10.1007/s11926-018-0732-6.
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J Investig Med High Impact Case Rep. 2017 Jun 14;5(2):2324709617709031. doi: 10.1177/2324709617709031. eCollection 2017 Apr-Jun.
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Advances in serological diagnostics of inflammatory myopathies.炎症性肌病血清学诊断的进展
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