Evaluation and treatment of inflammatory myopathies

被引:84
作者
Amato, A. A. [1 ]
Barohn, R. J. [2 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66103 USA
关键词
INCLUSION-BODY MYOSITIS; REFRACTORY JUVENILE DERMATOMYOSITIS; MONOCLONAL-ANTIBODY ANALYSIS; SIGNAL RECOGNITION PARTICLE; NECROSIS-FACTOR-ALPHA; MYCOPHENOLATE-MOFETIL; POLYMYOSITIS-DERMATOMYOSITIS; CYCLOPHOSPHAMIDE THERAPY; NECROTIZING MYOPATHY; PLASMA-EXCHANGE;
D O I
10.1136/jnnp.2008.169375
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
The major types of idiopathic inflammatory myopathy include dermatomyositis (DM), polymyositis (PM), inclusion body myositis (IBM) and immune mediated necrotising myopathy (NM). These myositides appear clinically, histologically and pathogenically distinct. DM, PM and immune mediated NM are responsive to immunosuppressive therapy, in contrast with IBM which is generally refractory to therapy. Greater understanding of the pathogenic bases of these disorders should hopefully lead to better treatment. We need well designed, prospective, double blind, placebo controlled trials in order to determine the best therapeutic options for these different disorders.
引用
收藏
页码:1060 / 1068
页数:9
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