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[A parietal form of Pick's disease: clinical and pathological study (author's transl)].

作者信息

Cambier J, Masson M, Dairou R, Henin D

出版信息

Rev Neurol (Paris). 1981;137(1):33-8.

PMID:7232964
Abstract

A patient developed a neurological disorder at the age of 57 years and died 9 years later after progressive aggravation. The clinical picture was that of a unilateral, parietal, focal neurological syndrome for many years, finally becoming bilateral. The purely neurological nature of the condition, without signs of mental disturbance, should be emphasized. Pathological examination showed mainly unilateral circumscribed cortical atrophy in the parietal regions. Histological examination showed atrophic lesions typical of Pick's disease. This case provides suggestive evidence for the existence of purely parietal forms of Pick's disease.

摘要

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引用本文的文献

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Posterior cortical atrophy: variant of Alzheimer's disease? A case series with PET findings.后皮质萎缩:阿尔茨海默病的变异型?一项PET检查结果的病例系列研究
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Corticobasal ganglionic degeneration and/or frontotemporal dementia? A report of two overlap cases and review of literature.皮质基底节变性和/或额颞叶痴呆?两例重叠病例报告及文献综述。
J Neurol Neurosurg Psychiatry. 2000 Mar;68(3):304-12. doi: 10.1136/jnnp.68.3.304.
3
Slowly progressive apraxia: two case studies.
J Neurol. 1993 Jun;240(6):347-50. doi: 10.1007/BF00839965.
4
Quantitative neuropathologic analysis of Pick's disease cases: cortical distribution of Pick bodies and coexistence with Alzheimer's disease.匹克氏病病例的定量神经病理学分析:匹克小体的皮质分布及与阿尔茨海默病的共存情况
Acta Neuropathol. 1994;87(2):115-24. doi: 10.1007/BF00296179.
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Striatonigral degeneration, olivopontocerebellar atrophy and "atypical" Pick disease.纹状体黑质变性、橄榄脑桥小脑萎缩和“非典型”皮克病。
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