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特发性炎性肌病进展 被引量：8

The advance of idiopathic inflammatory myopathy
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摘要 特发性炎性肌病（IIM）是一组具有不同临床表现和病理学特点的骨骼肌免疫性疾病,通常包括多发性肌炎（PM）、皮肌炎（DM）、免疫性坏死性肌病（NAM）、包涵体肌炎（IBM）、结缔组织病相关性免疫性坏死性肌病和罕见类型的炎性肌病。炎性肌病不同类型构成比随疾病研究的深入显著改变,其中95%曾诊断的多发性肌炎重新经病理学和免疫学评估而改变诊断。多发性肌炎除名称外可能已不复存在，更多可能是伴特殊抗体的炎性肌病、重叠性肌炎或结缔组织病相关性免疫性坏死性肌病，疾病谱的改变需临床医师重新认识不同炎性肌病的临床表现。
作者 袁云
机构地区 北京大学第一医院神经内科
出处 《中国现代神经疾病杂志》 CAS 2016年第10期647-650,共4页 Chinese Journal of Contemporary Neurology and Neurosurgery
基金 国家科技重大专项课题-重大新药创制(项目编号:2011ZX09307-001-07)Projects(No.2011ZX09307-001-07)~~
关键词 肌炎 综述 Myositis Review
分类号 R593.2 [医药卫生—内科学]
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参考文献33

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  • 3Vilela VS, Prieto-Gonzdlez S, Milisenda JC, Selva-O Callaghan A, Grau JM. Polymyositis, a very uncommon isolated disease: clinical and histological re-evaluation after long-term follow-up. Rheumatol Int, 2015, 35:915-920. 被引量：1
  • 4Tansley SL, McHugh N J, Wedderburn LR. Adult and juvenile dermatomyositis: are the distinct clinical features explained by our current understanding of serological subgroups and pathogenic mechanisms? Arthritis Res Ther, 2013, 15:211. 被引量：1
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二级参考文献16

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  • 4Wemer JL, Christopher-Stine L, Ghazarian SR, et al. Antibody levels correlate with creatine kinase levels and strength in anti-3- hydroxy-3-methylglutaryl-coenzyme A reductase-associated autoimmune myopathy [ J]. Arthritis Rheum, 2012, 64 ( 12 ) : 4087 -4093. 被引量：1
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  • 10Meriggioli MN, Barboi AC, Rowin J, et al. HMG-CoA reductase inhibitor myopathy: clinical, electrophysiological, and pathologic data in five patients[ J]. J Clin Neuromuscul Dis, 2001, 2 (3) : 129-134. 被引量：1

共引文献6

同被引文献26

引证文献8

二级引证文献8

中国现代神经疾病杂志
2016年 第10期

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