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A patient with multiple system atrophy presenting prolonged levodopa-responsive parkinsonism and off-dystonia of the trunk

机译:多系统萎缩症患者出现左旋多巴反应性帕金森病延长和躯干肌张力障碍

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摘要

A 46-year-old man had a 7-year history of dopa-responsive parkinsonism. Four years after starting levodopa, he had typical motor complications such as wearing-off and peak dose as well as off-period dystonia of his trunk. Brain MRI showed marked atrophy of the brainstem and cerebellum, and the cross sign was present in the pontine base. There was neither abnormal signal intensity nor atrophy in the basal ganglia. Then, he was suspected as having multiple system atrophy (MSA). It is not easy to differentiate MSA from Parkinson diseases, particularly when the patient shows good response to levodopa and motor complications like those seen in Parkinson's disease. If the striatal pathology was not severe and nigral degeneration was prominent, presynaptic parkinsonism might occur in MSA, and putaminal preservation might account for good response to levodopa therapy. In patients with MSA, disproportionate antecollis is common before levodopa treatment, and levodopa induced off-dystonia of his trunk is very rare.
机译:一名46岁的男子有7年多巴反应性帕金森病史。开始左旋多巴后的四年,他患有典型的运动并发症,例如,躯干衰弱,峰值剂量以及躯干期肌张力障碍。脑部MRI显示脑干和小脑明显萎缩,桥脑基底出现十字标志。基底神经节既没有异常的信号强度也没有萎缩。然后,他被怀疑患有多系统萎缩症(MSA)。很难将MSA与帕金森病区分开来,特别是当患者对左旋多巴和运动并发症如帕金森氏病中表现出良好的反应时。如果纹状体病理学不严重且黑质变性明显,则MSA中可能发生突触前帕金森氏综合征,而腹膜保存可能说明对左旋多巴治疗的良好反应。在MSA患者中,左旋多巴治疗前常见比例过高的前毛囊,左旋多巴引起的躯干肌张力异常非常罕见。

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