TAU, UBIQUITIN, AND ALPHA-BETA-CRYSTALLIN IMMUNOHISTOCHEMISTRY DEFINE THE PRINCIPAL CAUSES OF DEGENERATIVE FRONTOTEMPORAL DEMENTIA

被引:111
作者
COOPER, PN
JACKSON, M
LENNOX, G
LOWE, J
MANN, DMA
机构
[1] UNIV MANCHESTER, SCH MED, DEPT PATHOL, DIV MOLEC PATHOL, MANCHESTER, LANCS, ENGLAND
[2] UNIV NOTTINGHAM, SCH MED, QUEENS MED CTR, DEPT PATHOL, NOTTINGHAM, ENGLAND
关键词
D O I
10.1001/archneur.1995.00540340103019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We investigated the use of immunostaining with antibodies to tau, ubiquitin, and alpha B-crystallin in defining a protocol for the staged neuropathologic examination of brains from patients with a progressive frontotemporal dementia. Design: Brains obtained from 50 patients dying with the clinical diagnosis of frontotemporal dementia were examined histopathologically to define pathologic distinctions. Setting: Two university hospital neuropathology departments. Results: Anti-tau immunostaining defined corticobasal degeneration, Alzheimer's disease, and Pick's disease; antiubiquitin defined motor neuron disease with dementia. The remaining brains have frontal lobe degeneration: the use of alpha B-crystallin immunostaining, on these, to detect ballooned neurons may help to define two groups of patients, one of which we believe may represent a variant of Pick's disease. Conclusion: These findings indicate that immunostaining with these antibodies is essential for the evaluation of frontal dementia.
引用
收藏
页码:1011 / 1015
页数:5
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