Autoimmune Myopathies
- PMID: 30422455
- Bookshelf ID: NBK532860
Autoimmune Myopathies
Excerpt
Idiopathic inflammatory myositis (IIM) is classified into four subtypes based on clinical and histopathological features. Polymyositis and dermatomyositis (PM/DM) are two of those subtypes, in addition to immune-mediated necrotizing myopathy and inclusion body myositis. The presence of autoantibodies and inflammatory infiltration in the muscles suggests that idiopathic inflammatory myositis is an autoimmune condition, but the target autoantigens have not yet been identified. Apart from symmetric proximal muscle weakness, polymyositis and dermatomyositis (DM) have several clinical manifestations in common when compared to inclusion body myositis and necrotizing myopathy and can be grouped for discussion.
The most commonly used criteria for PM/DM are Peter/Bohan criteria.
Symmetric proximal muscle weakness
Elevated serum muscle enzymes
Myopathic changes in electromyography (EMG)
Characteristic muscle biopsy abnormalities
Typical rash of dermatomyositis
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References
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