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Status dystonicus and rhabdomyolysis in a patient with subacute sclerosing panencephalitis

机译:亚急性硬化性全脑炎患者的肌张力障碍和横纹肌溶解状态

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Subacute sclerosing panencephalitis (SSPE) is an uncommon presentation of measles virus infection in the central nervous system. The condition appears to result from mutations in the matrix protein, fusion protein, or hemagglutinin of the measles virus, which allow the virus to spread throughout the brain. Dystonia is a neurological movement disorder, in which sustained muscle contractions cause twisting and repetitive movements or abnormal postures. Patients with dystonia sometimes develop increasingly frequent and relentless episodes of devastating generalized dystonia, which is called status dystonicus or dystonic storm. Dystonia has been described in a few cases with SSPE, but status dystonicus has not been reported before. On the other hand, there are a few cases of rhabdomyolysis associated with dystonia. Here, we describe a patient with SSPE who had rhabdomyolysis due to status dystonicus.
机译:亚急性硬化性全脑炎(SSPE)是中枢神经系统中麻疹病毒感染的罕见表现。该病似乎是由麻疹病毒的基质蛋白,融合蛋白或血凝素突变引起的,这种突变可使病毒在整个大脑中传播。肌张力障碍是一种神经系统运动障碍,其中持续的肌肉收缩会导致扭曲和重复性运动或异常姿势。肌张力障碍患者有时会出现越来越频繁且持续不断的毁灭性泛发性肌张力障碍,称为状态性肌张力障碍或肌张力障碍。在少数使用SSPE的病例中已描述了肌张力障碍,但以前尚未报告肌张力障碍状态。另一方面,有少数与肌张力障碍有关的横纹肌溶解病例。在这里,我们描述了由于状态肌张力障碍而发生横纹肌溶解的SSPE患者。

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