DERMATOMYOSITIS AND POLYMYOSITIS UPDATE ON CURRENT CONTROVERSIES
Identifieur interne : 003353 ( Main/Exploration ); précédent : 003352; suivant : 003354DERMATOMYOSITIS AND POLYMYOSITIS UPDATE ON CURRENT CONTROVERSIES
Auteurs : Jeffrey P. Callen [États-Unis]Source :
- Australasian Journal of Dermatology [ 0004-8380 ] ; 1987-08.
Abstract
Polymyositis and dermatomyositis are syndromes of unknown aetiology which are systemic in their nature involving prominent skin disease and prominent muscle disease. Classification is important particularly since dermatomyositis may be associated with malignancy more frequently than polymyositis, and certain subsets such as overlap syndromes less frequently harbour malignancy. Poor prognosic signs include pulmonary disease, the presence of malignancy, the severity of the weakness, and the presence of oesophageal disease. Therapy with corticosteroids is generally effective. In those patients who develop steroid side effects, immunosuppressive agents may be of use. Cutaneous disease may be controlled with hydroxychloroquine therapy.
Url:
DOI: 10.1111/j.1440-0960.1987.tb00336.x
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Polymyositis and dermatomyositis are syndromes of unknown aetiology which are systemic in their nature involving prominent skin disease and prominent muscle disease. Classification is important particularly since dermatomyositis may be associated with malignancy more frequently than polymyositis, and certain subsets such as overlap syndromes less frequently harbour malignancy. Poor prognosic signs include pulmonary disease, the presence of malignancy, the severity of the weakness, and the presence of oesophageal disease. Therapy with corticosteroids is generally effective. In those patients who develop steroid side effects, immunosuppressive agents may be of use. Cutaneous disease may be controlled with hydroxychloroquine therapy.</div>
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