Neurofibrillary tangle-predominant dementia: Comparison with classical Alzheimer disease

被引:117
作者
Jellinger, K. A.
Attems, J.
机构
[1] Inst Clin Neurobiol, A-1070 Vienna, Austria
[2] OWS Hosp, Dept Pathol, Vienna, Austria
关键词
senile dementia with tangles; Alzheimer disease; 3 and 4 repeat tau isoforms; tauopathy; differential diagnosis; neuropathology; ARGYROPHILIC GRAIN DISEASE; PROGRESSIVE SUPRANUCLEAR PALSY; CEREBRAL AMYLOID ANGIOPATHY; APOLIPOPROTEIN-E EPSILON-2; GLIAL FIBRILLARY TANGLES; SENILE-DEMENTIA; CORTICOBASAL DEGENERATION; PICKS-DISEASE; HIPPOCAMPAL SCLEROSIS; MONOCLONAL-ANTIBODIES;
D O I
10.1007/s00401-006-0156-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neurofibrillary tangle predominant dementia (NFTPD) is a subset of late onset dementia, clinically different from traditional "plaque and tangle" Alzheimer disease (AD): later onset, shorter duration, less severe cognitive impairment, and almost absence of ApoE epsilon 4. Neuropathology reveals abundant allocortical neurofibrillary pathology with no or few isocortical tau lesions, absence of neuritic plaques, absence or scarcity of amyloid deposits, but neurofibrillary changes comprising both 3 and 4 repeat (3R and 4R) tau immunohistochemistry are not significantly different from those in classical AD. Comparing 51 autopsy cases of NFTPD with 244 classical AD subjects, the nosology of NFTPD and its differences from AD are discussed.
引用
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页码:107 / 117
页数:11
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