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[血管性帕金森综合征]

[Vascular parkinsonian syndrome].

作者信息

Ebersbach G, Poewe W

机构信息

Fachkrankenhaus für Bewegungsstörungen/Parkinson, Beelitz-Heilstätten.

出版信息

Nervenarzt. 2006 Feb;77(2):139-44, 146-7. doi: 10.1007/s00115-005-1978-6.

Abstract

The present review shows that vascular parkinsonian syndrome (VPS) fulfilling stringent diagnostic criteria for parkinsonism is a rare disease that cannot always be distinguished from neurodegenerative parkinsonism on clinical grounds. Thus VPS needs to be differentiated from other disturbances, which have distinct phenomenological and therapeutical features including isolated gait disturbances associated with subcortical arteriosclerotic encephalopathy and neurodegenerative parkinsonism complicated by comorbid vascular encephalopathy. Acute or subacute VPS is usually caused by contralateral infarctions involving the external globus pallidus, ventrolateral thalamus, and, less often, the substantia nigra. Chronic VPS with insidious onset is related to bilateral subcortical infarctions affecting thalamocortical projections. Differentiation from degenerative parkinsonism is difficult in cases of VPS that display a progressive course and response to levodopa.

摘要

本综述表明,符合帕金森病严格诊断标准的血管性帕金森综合征(VPS)是一种罕见疾病,在临床上并不总是能与神经退行性帕金森病区分开来。因此,VPS需要与其他具有不同现象学和治疗特征的疾病相鉴别,这些疾病包括与皮质下动脉硬化性脑病相关的孤立性步态障碍以及合并血管性脑病的神经退行性帕金森病。急性或亚急性VPS通常由累及外侧苍白球、丘脑腹外侧核,较少累及黑质的对侧梗死引起。隐匿起病的慢性VPS与影响丘脑皮质投射的双侧皮质下梗死有关。在表现为进行性病程且对左旋多巴有反应的VPS病例中,与退行性帕金森病的鉴别较为困难。

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