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无症状高肌酸激酶患者的免疫介导性坏死性肌病。

Immune-mediated necrotising myopathy in asymptomatic patients with high creatine kinase.

机构信息

Neurosciences, Centro Universitário Saúde ABC, Santo Andre, São Paulo, Brazil.

Neurosciences, Centro Universitário Saúde ABC, Santo Andre, São Paulo, Brazil

出版信息

BMJ Case Rep. 2020 Oct 8;13(10):e235457. doi: 10.1136/bcr-2020-235457.

Abstract

Subacute symmetrical proximal muscle weakness and persistent elevated creatine kinase levels are typical of immune-mediated necrotising myopathy (IMNM). These conditions are accompanied by copious myofibre necrosis, degeneration and regeneration with minimal to no inflammation on muscle biopsy. We report two cases (case 1 and case 2) of asymptomatic IMNM from different families with hyperCKaemia associated with positive anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies, respectively, and we also reviewed the literature. There are only a few previous descriptions of patients with asymptomatic IMNM.The disease onset could be insidious and lead to delayed diagnosis and treatment. We recommend testing for the anti-HMGCR and anti-SRP antibodies in patients with idiopathic hyperCKaemia because they could show no symptoms of this disorder.

摘要

亚急性对称性近端肌无力和持续升高的肌酸激酶水平是免疫介导的坏死性肌病(IMNM)的典型特征。这些病症伴随着大量肌纤维坏死、变性和再生,肌肉活检显示炎症很少或没有。我们报告了两例来自不同家族的无症状 IMNM 病例(病例 1 和病例 2),分别与高肌酸激酶血症相关的抗信号识别颗粒(SRP)和抗 3-羟基-3-甲基戊二酰辅酶 A 还原酶(HMGCR)抗体阳性有关,并且我们还回顾了文献。以前只有少数关于无症状 IMNM 患者的描述。疾病的发作可能是隐匿的,导致诊断和治疗延迟。我们建议对特发性高肌酸激酶血症患者进行抗 HMGCR 和抗 SRP 抗体检测,因为他们可能没有这种疾病的症状。

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本文引用的文献

1
Anti-HMGCR myopathy may resemble limb-girdle muscular dystrophy.抗 HMGCR 肌病可能类似于肢带型肌营养不良症。
Neurol Neuroimmunol Neuroinflamm. 2018 Dec 12;6(1):e523. doi: 10.1212/NXI.0000000000000523. eCollection 2019 Jan.
8
Cancer association as a risk factor for anti-HMGCR antibody-positive myopathy.癌症关联作为抗HMGCR抗体阳性肌病的一个风险因素。
Neurol Neuroimmunol Neuroinflamm. 2016 Oct 7;3(6):e290. doi: 10.1212/NXI.0000000000000290. eCollection 2016 Dec.

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