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伴周围神经损害的抗SRP抗体及抗GT1a抗体双阳性免疫介导坏死性肌病1例报告OACSTPCD

Immune-mediated necrotizing myopathy with positive anti-signal recognition particle antibody and anti-GT1a an-tibody accompanied by peripheral nerve injury:a case report

中文摘要英文摘要

抗信号识别颗粒(SRP)坏死性肌病属于免疫介导坏死性肌病(IMNM)的一种类型.该病临床少见,起病隐袭,进展较快,主要表现为对称性四肢近端无力及肌酸激酶显著升高.本文报道1例合并周围神经病变的血清抗SRP抗体及抗GT1a抗体双阳性患者,分析其临床资料及诊治经过,以提高临床医生对该病的认识.

Anti-signal recognition particle(SRP)necrotizing myopathy is a type of immune-mediated necrotizing myopathy(IMNM).It is a rare disease in clinical practice and has the features of insidious onset and rapid progression,with the main manifestations of symmetrical proximal limb weakness and a significant increase in creatine kinase.This ar-ticle reports a patient with positive serum anti-SRP antibody and anti-GT1a antibody accompanied by peripheral neuropa-thy and analyze related clinical data and diagnosis and treatment processes,in order to improve the understanding of this disease among clinicians.

张忠胜;黄嘉星;孔学健

广州医科大学附属第六医院(清远市人民医院)神经内科,广东 清远 511518

临床医学

信号识别颗粒坏死性肌病肢体乏力

Signal recognition particleNecrotizing myopathyLimb weakness

《中风与神经疾病杂志》 2024 (006)

560-562 / 3

10.19845/j.cnki.zfysjjbzz.2024.0107

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