Author:
Rose M. R.,Kissel J. T.,Bickley L. S.,Griggs R. C.
Abstract
We describe two patients with sustained myoglobinuria that did not resolve with supportive treatment.After we established a diagnosis of dermatomyositis and started treatment with corticosteroids, there was rapid resolution of the myoglobinuria. Well-documented cases of inflammatory myopathy causing myoglobinuria are rare, but their prompt recognition has important therapeutic implications.NEUROLOGY 1996;47: 119-123
Publisher
Ovid Technologies (Wolters Kluwer Health)
Reference29 articles.
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2. Walton JN, Adams RD. Polymyositis. Edinburgh: Livingstone, 1958.
Cited by
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