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未经治疗的帕金森病中的肌张力障碍

Dystonia in untreated parkinsonism.

作者信息

LeWitt P A, Burns R S, Newman R P

出版信息

Clin Neuropharmacol. 1986;9(3):293-7. doi: 10.1097/00002826-198606000-00007.

Abstract

While parkinsonism and dystonia generally are distinct clinical syndromes, both may be prominent features even prior to the use of antiparkinsonian medications. In 10 patients with typical parkinsonism, coincident dystonic features included neck, upper extremity, oromandibular, unilateral upper-lower extremity, and unilateral foot dystonia. Six patients were first affected before the age of 45. For some, dystonia preceded parkinsonism (for 1/2 to 20 years). Limb symptoms tended to be unilateral; in seven patients, parkinsonism also was limited to that side. While levodopa was adequate for improvement of parkinsonism, dystonic symptoms benefited from the combination of levodopa with a dopaminergic ergot. The dystonic features (which also can result from parkinsonian therapy) often add pain and disability to the deficits in parkinsonism. The coexistence of dystonia may constitute a distinctive syndrome of parkinsonism and points to possible etiologic mechanisms shared by these two extrapyramidal disorders.

摘要

虽然帕金森综合征和肌张力障碍通常是不同的临床综合征,但在使用抗帕金森药物之前,两者都可能是突出的特征。在10例典型帕金森综合征患者中,同时出现的肌张力障碍特征包括颈部、上肢、口下颌、单侧上肢-下肢和单侧足部肌张力障碍。6例患者在45岁之前首次发病。对一些患者来说,肌张力障碍先于帕金森综合征出现(持续1/2至20年)。肢体症状往往是单侧的;7例患者的帕金森综合征也局限于同一侧。虽然左旋多巴足以改善帕金森综合征,但肌张力障碍症状受益于左旋多巴与多巴胺能麦角碱的联合使用。肌张力障碍特征(也可能由帕金森病治疗引起)常常给帕金森综合征的缺陷增加疼痛和残疾。肌张力障碍的共存可能构成一种独特的帕金森综合征,并指出这两种锥体外系疾病可能共有的病因机制。

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