1. Sorting through the idiopathic inflammatory myopathies.
- Author
-
Wallace EA, Adelson D, and Wortmann RL
- Abstract
The idiopathic inflammatory myopathies, including polymyositis, dermatomyositis, and inclusion body myositis, present with proximal muscle weakness. The diagnosis can be made only after the exclusion of other causes of abnormalities. Steps in making the diagnosis include determining the time course and characteristics of the weakness, its effect on the patient's daily life, and associated symptoms. The examination should focus on specific muscle groups. An elevated serum creatine kinase level may be the most sensitive laboratory test. Myositis-specific autoantibodies are found exclusively in patients who have an idiopathic inflammatory myopathy. The diagnosis can be suggested by electromyography or MRI. Medical treatment often requires the use of immunosuppressive agents over long periods. Corticosteroids are used as first-line therapy to decrease inflammation. [ABSTRACT FROM AUTHOR]
- Published
- 2006