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From the Departments of Neurology (Drs. Rose and Griggs) and Medicine (Drs. Bickley and Griggs), University of Rochester Medical Center, Rochester, NY; and the Department of Neurology (Dr. Kissel), The Ohio State University Hospitals, Columbus OH.
M.R. Rose is a visiting fellow supported by the W.A. Young Charitable Trust; The Muscular Dystrophy Association of Great Britain; The King Edward's Hospital Fund, London; The Guarantors of Brain; The Mercer's Company; and Sanofi Winthrop U.K.
Received October 10, 1995. Accepted in final form January 9, 1996.
Address correspondence and reprint requests to Dr Rose, Dept. of Neurosciences, Kings College Hospital, Denmark Hill, London, England SE5 9RS.
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
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