Rose M R, Kissel J T, Bickley L S, Griggs R C
Department of Neurology, University of Rochester Medical Center, NY, USA.
Neurology. 1996 Jul;47(1):119-23. doi: 10.1212/wnl.47.1.119.
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.
我们描述了两名持续性肌红蛋白尿患者，他们接受支持性治疗后病情并未缓解。在我们确诊为皮肌炎并开始使用皮质类固醇治疗后，肌红蛋白尿迅速消退。有充分记录的炎症性肌病导致肌红蛋白尿的病例很少见，但对其迅速识别具有重要的治疗意义。
