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[迟发性脊髓小脑变性伴肌萎缩,并发严重苍白球-路易体变性及弥漫性老年组织学病变。(1例病例的解剖学-临床研究及疾病分类学讨论)]

[Tardive spino-cerebellar degeneration with amyotrophia, complicating a severe case of pallido-luysian degeneration and diffuse histological lesions of senility. (Anatomo-clinical study of a case with nosographic discussion)].

作者信息

Boudouresques J, Toga M, Khalil R, Chérif A A, Pellissier J F, Gosset A

出版信息

Rev Neurol (Paris). 1976 Sep;132(9):623-37.

PMID:996389
Abstract

Anatomo-clinical findings are reported in a case of central nervous system degeneration which began at age 47 and progressed over a three year period. Information obtained prior to the patient's death suggested probable spinocerebellar degeneration with amyotrophies. Postmortem anatomical examination confirmed this diagnosis but also revealed the existence of unsuspected lesions. These clinically non-manifested lesions involved severe pallido-luysian degeneration as well as numerous and diffuse senile plaques. The nosological implications of this case are discussed.

摘要

报告了一例中枢神经系统变性病例的解剖学临床发现,该病例始于47岁,病程长达三年。患者死亡前获得的信息提示可能为伴有肌萎缩的脊髓小脑变性。尸检解剖证实了这一诊断,但也发现了意外病变。这些临床上未表现出的病变包括严重的苍白球-路易体变性以及大量弥漫性老年斑。讨论了该病例的疾病分类学意义。

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引用本文的文献

1
[Morbus Gerstmann-Sträussler-Scheinker. The Sch. family-a report of three cases (author's transl)].[格斯特曼-施特劳斯勒-申克病。施氏家族——三例报告(作者译)]
Arch Psychiatr Nervenkr (1970). 1981;230(3):179-96. doi: 10.1007/BF00344444.
2
Luyso-pallido-nigral atrophy and amyotrophic lateral sclerosis.
Acta Neuropathol. 1985;66(1):78-82. doi: 10.1007/BF00698300.
3
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?).家族性阿尔茨海默病中的小脑斑块(格斯特曼-施特劳斯勒-谢因克变异型?)
Acta Neuropathol. 1985;65(3-4):235-46. doi: 10.1007/BF00687003.