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非阿尔茨海默病性额颞叶变性痴呆。一项神经行为学与病理学研究。

Non-Alzheimer fronto-temporal degenerative dementia. A neurobehavioral and pathologic study.

作者信息

Filley C M, Kleinschmidt-De Masters B K, Gross K F

机构信息

Department of Neurology, University of Colorado Health Science Center, Denver 80262.

出版信息

Clin Neuropathol. 1994 May-Jun;13(3):109-16.

PMID:8088029
Abstract

In contrast to Alzheimer's disease (AD), which predominantly affects the limbic system and association neocortex, degenerative dementias have been identified that show greatest damage in frontal and temporal neocortex. This "lobar atrophy" was first described by Arnold Pick over 100 years ago. We present four autopsy-documented, non-AD cases of fronto-temporal degeneration (FTD), each with neurobehavioral assessment. Three of the patients presented with personality change and the fourth with non-fluent aphasia; memory was initially preserved in all, and only later did dementia become evident. At autopsy, the hippocampi were relatively spared in all cases. One patient had classic Pick-body temporal lobe Pick's disease (PD), 2 had frontal lobe-predominant atrophy with severe degeneration of caudate and substantia nigra (so-called "generalized Pick's"), and the fourth had temporal lobe degeneration without Pick bodies or cells. We propose that subgroups of FTD be categorized both by microscopic features and gross patterns of atrophy, and that subgroups of FTD be kept separate for neurochemical and genetic studies. Neurobehavioral and neuropsychological evaluation early in the course of unusual degenerative dementia can aid in distinguishing FTD cases from AD patients for clinical and drug studies.

摘要

与主要影响边缘系统和联合新皮质的阿尔茨海默病(AD)不同,已发现某些退行性痴呆在额叶和颞叶新皮质中损伤最为严重。这种“脑叶萎缩”早在100多年前就由阿诺德·皮克首次描述。我们展示了4例经尸检证实的非AD型额颞叶变性(FTD)病例,并对每例进行了神经行为评估。其中3例患者表现为性格改变,第4例表现为非流畅性失语;所有患者最初记忆力均得以保留,痴呆症状仅在后期才明显显现。尸检时,所有病例的海马体相对未受影响。1例患者患有典型的伴有Pick小体的颞叶皮克病(PD),2例患者额叶萎缩为主,尾状核和黑质严重变性(即所谓的“泛化型皮克病”),第4例患者颞叶变性但无Pick小体或细胞。我们建议,FTD的亚组应根据微观特征和萎缩的大体模式进行分类,并且在神经化学和遗传学研究中应将FTD的亚组区分开来。在不寻常的退行性痴呆病程早期进行神经行为和神经心理学评估,有助于在临床和药物研究中将FTD病例与AD患者区分开来。

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