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一名患有多系统萎缩的患者,表现为左旋多巴反应性帕金森病持续时间延长及躯干异动症(关期)

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

作者信息

Nakanishi Ichiro, Hironishi Masaya, Miwa Hideto, Kondo Tomoyoshi

机构信息

Department of Neurology, Wakayama Medical University, Kimiidera 811-1, Wakayama-City, 641-8510, Japan.

出版信息

No To Shinkei. 2003 Jul;55(7):605-8.

Abstract

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.

摘要

一名46岁男性有7年多巴反应性帕金森综合征病史。开始使用左旋多巴4年后,他出现了典型的运动并发症,如疗效减退、剂峰异动症以及躯干的剂末肌张力障碍。脑部MRI显示脑干和小脑明显萎缩,脑桥基底部出现交叉征。基底节区既无异常信号强度也无萎缩。随后,他被怀疑患有多系统萎缩(MSA)。将MSA与帕金森病区分并不容易,尤其是当患者对左旋多巴表现出良好反应且出现帕金森病中所见的运动并发症时。如果纹状体病变不严重且黑质变性突出,MSA可能会出现突触前帕金森综合征,而壳核保留可能解释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不成比例的颈前屈,而左旋多巴诱发的躯干剂末肌张力障碍非常罕见。

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