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运动神经元病中的帕金森综合征:病例报告及文献综述

Parkinsonism in motor neuron disease: case report and literature review.

作者信息

Williams T L, Shaw P J, Lowe J, Bates D, Ince P G

机构信息

Division of Clinical Neuroscience, Royal Victoria Infirmary, Newcastle upon Tyne, UK.

出版信息

Acta Neuropathol. 1995;89(3):275-83. doi: 10.1007/BF00309344.

DOI:10.1007/BF00309344
PMID:7754748
Abstract

This report describes a patient who had clinical features of both motor neuron disease and Parkinson's disease. Neuropathological examination and immunocytochemical studies showed that he had motor neuron disease of the progressive muscular atrophy type, and Lewy body Parkinson's disease, with intracytoplasmic inclusion bodies characteristic of both conditions. This is the first detailed description of these two diseases occurring concurrently in the same patient. A review of all previously reported cases of combined motor neuron disease and parkinsonism has led to the following conclusions: (1) that these two neuropathologically defined diseases occur together very infrequently, but (2) that parkinsonism and substantia nigra degeneration are not uncommon as part of the multi-system disease process underlying motor neuron disease.

摘要

本报告描述了一名同时具有运动神经元病和帕金森病临床特征的患者。神经病理学检查和免疫细胞化学研究表明,他患有进行性肌萎缩型运动神经元病和路易体帕金森病,伴有两种疾病特有的胞质内包涵体。这是首次对同一患者同时发生这两种疾病的详细描述。对所有先前报道的运动神经元病合并帕金森综合征病例的回顾得出以下结论:(1)这两种神经病理学定义的疾病同时发生的情况非常罕见,但(2)帕金森综合征和黑质变性作为运动神经元病潜在多系统疾病过程的一部分并不少见。

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本文引用的文献

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Arch Neurol. 1962 Sep;7:227-42. doi: 10.1001/archneur.1962.04210030065009.
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neural muscle atrophy with degeneration of the substantia nigra.伴有黑质变性的神经肌肉萎缩
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Tabes of Friedreich with degeneration of the substantia nigra, a special type of hereditary parkinsonism.伴有黑质变性的弗里德赖希共济失调,一种特殊类型的遗传性帕金森病。
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[Typical amyotrophic lateral sclerosis and hereditary paralysis agitans in the same family with the possibility of a form transitional between the two].[同一家族中典型的肌萎缩侧索硬化症和遗传性帕金森震颤麻痹,两者之间可能存在一种过渡形式]
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