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一例成人起病的单纯苍白球变性。I. 临床表现及神经病理学观察。

A case of adult onset pure pallidal degeneration. I. Clinical manifestations and neuropathological observations.

作者信息

Aizawa H, Kwak S, Shimizu T, Goto J, Nakano I, Mannen T, Shibasaki H

机构信息

National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.

出版信息

J Neurol Sci. 1991 Mar;102(1):76-82. doi: 10.1016/0022-510x(91)90096-p.

Abstract

We present a case of adult onset progressive neurodegenerative disease with a selective involvement in the globus pallidus (GP). The main symptom was extreme slowness in motion without rigidity, which was distinct from akinesia of parkinsonism. Dystonic posture developed in neck and fingers and mild rigidospasticity appeared in a later stage. Neuropathological examination shows a selective neuronal loss with gliosis in GP and degeneration of the efferent fibers. Although the subthalamic nucleus is slightly atrophic with minimal gliosis, there is no neuronal loss in the nucleus. The rest of the structures are pathologically insignificant. Because the pathological change is confined to GP neurons and their efferent fibers, we think that the marked slowness in motion and dystonic posture are ascribable to the selective GP lesion. A degenerative neurological disorder preferentially involved in GP was reported as pure pallidal degeneration (PPD). The onset of the PPD was in the first or second decades and the main symptoms were choreoathetosis, torsion dystonia and progressive rigidity. These distinct clinical features seemed to distinguish the present case from the previously described PPD. Therefore, we would like to call our case "adult onset" PPD. Clinicopathological correlation is discussed.

摘要

我们报告一例成人起病的进行性神经退行性疾病,其选择性累及苍白球(GP)。主要症状为运动极度迟缓但无强直,这与帕金森病的运动不能不同。颈部和手指出现肌张力障碍姿势,后期出现轻度强直痉挛。神经病理学检查显示苍白球有选择性神经元丢失伴胶质增生以及传出纤维变性。尽管丘脑底核轻度萎缩且胶质增生轻微,但该核内无神经元丢失。其余结构在病理上无明显异常。由于病理改变局限于苍白球神经元及其传出纤维,我们认为明显的运动迟缓及肌张力障碍姿势可归因于选择性苍白球病变。一种优先累及苍白球的退行性神经疾病被报道为纯苍白球变性(PPD)。PPD发病于第一或第二个十年,主要症状为舞蹈手足徐动症、扭转肌张力障碍和进行性强直。这些明显的临床特征似乎将本病例与先前描述的PPD区分开来。因此,我们将我们的病例称为“成人起病型”PPD。本文讨论了临床病理相关性。

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