Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

被引:131
作者
Josephs, KA
Holton, JL
Rossor, MN
Godbolt, AK
Ozawa, T
Strand, K
Khan, N
Al-Sarraj, S
Revesz, T [1 ]
机构
[1] UCL, Inst Neurol, Div Neuropathol, London WC1N 3BG, England
[2] Kings Coll London, Inst Psychiat, Dept Neuropathol, London WC2R 2LS, England
[3] Mayo Clin, Dept Neurol, Rochester, MN USA
[4] UCL, Inst Neurol, Dept Mol Neurosci, Queen Sq Brain Bank, London, England
[5] UCL, Inst Neurol, Dementia Res Grp, London, England
关键词
abnormal neurites; frontotemporal dementia; frontotemporal lobar degeneration; neuronal cytoplasmic inclusions; ubiquitin;
D O I
10.1111/j.1365-2990.2003.00545.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We set out to determine the frequency of the different pathologies underlying frontotemporal degeneration (FTD) in our brain bank series, by reviewing all cases of pathologically diagnosed FTD over the last 12 years. We identified and reviewed 29 cases of FTD and classified them using the most recent consensus criteria with further histological analysis of 6 initially unclassifiable cases. Detailed histological analysis of these 6 cases revealed variable numbers of ubiquitin-positive (tau and alpha-synuclein-negative) inclusions in 5 cases, consistent with the diagnosis of frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes (FTLD-U). As a consequence of the current re-evaluation, 18 (62%) of the 29 cases with FTD have underlying pathology consistent with FTLD-U. Therefore in our brain bank series of frontotemporal degeneration, most cases were non-tauopathies with FTLD-U accounting for 62% of all the diagnoses.
引用
收藏
页码:369 / 373
页数:5
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