Antemortem diagnosis of frontotemporal lobar degeneration

被引:151
作者
Knopman, DS
Boeve, BF
Parisi, JE
Dickson, DW
Smith, GE
Ivnik, RJ
Josephs, KA
Petersen, RC
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Dept Neurol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Pathol, Jacksonville, FL 32224 USA
[4] Mayo Clin, Coll Med, Dept Neurosci, Jacksonville, FL 32224 USA
[5] Mayo Clin & Mayo Fdn, Coll Med, Dept Psychiat & Psychol, Rochester, MN 55905 USA
关键词
D O I
10.1002/ana.20425
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The objective of this article is to study the accuracy of antemortem clinical diagnoses of frontotemporal lobar degenerations (FTLDs). From brain autopsies performed on subjects enrolled in the Mayo Alzheimer Center between 1991 and 2003, cases with neuropathological diagnoses of FTLD were identified. Neuropathological diagnoses of FTLDs were based on consensus criteria for FTLD. The initial clinical histories, neuropsychological test results, brain imaging studies, and initial clinical diagnoses were reviewed. There were 34 pathological FTLD cases among 433 subjects who underwent autopsy; 29 of these 34 cases were diagnosed as FTLD antemortem based on the sum of clinical, neuropsychological, and imaging features (sensitivity, 85%). The specificity was 99%. Among the 34 cases with pathological FTLD, 27 (79%) had clinical histories diagnostic of an FTLD syndrome, 20 (62%) had neuropsychological profiles consistent with FTLD, 17 (50%) had magnetic resonance scans consistent with FTLD, and 7 of 8 who had functional imaging studies had ones consistent with FTLD. In those with incorrect antemortem diagnoses, three were thought to have Alzheimer's disease, one was considered hard to classify, and one was diagnosed with vascular dementia. The antemortem consensus diagnosis of FTLD was moderately sensitive and very specific. With experienced clinicians and awareness of the unique manifestations of FTLD, accurate antemortem diagnosis was feasible.
引用
收藏
页码:480 / 488
页数:9
相关论文
共 75 条
[1]  
[Anonymous], 1997, Neurobiol Aging, V18, pS1
[2]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[3]   FRONTOTEMPORAL DEMENTIA AND ALZHEIMERS-DISEASE - RETROSPECTIVE DIFFERENTIATION USING INFORMATION FROM INFORMANTS [J].
BARBER, R ;
SNOWDEN, JS ;
CRAUFURD, D .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 59 (01) :61-70
[4]   KUFS DISEASE - A CRITICAL REAPPRAISAL [J].
BERKOVIC, SF ;
CARPENTER, S ;
ANDERMANN, F ;
ANDERMANN, E ;
WOLFE, LS .
BRAIN, 1988, 111 :27-62
[5]   Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS [J].
Bigio, EH ;
Lipton, AM ;
White, CL ;
Dickson, DW ;
Hirano, A .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2003, 29 (03) :239-253
[6]   Frontal lobe dementia with novel tauopathy: Sporadic multiple system tauopathy with dementia [J].
Bigio, EH ;
Lipton, AM ;
Yen, SH ;
Hutton, ML ;
Baker, M ;
Nacharaju, P ;
White, CL ;
Davies, P ;
Lin, WL ;
Dickson, DW .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2001, 60 (04) :328-341
[7]   Differences between Pick disease and Alzheimer disease in clinical appearance and rate of cognitive decline [J].
Binetti, G ;
Locascio, JJ ;
Corkin, S ;
Vonsattel, JP ;
Growdon, JH .
ARCHIVES OF NEUROLOGY, 2000, 57 (02) :225-232
[8]   Pathologic heterogeneity in clinically diagnosed corticobasal degeneration [J].
Boeve, BF ;
Maraganore, DM ;
Parisi, JE ;
Ahlskog, JE ;
Graff-Radford, N ;
Caselli, RJ ;
Dickson, DW ;
Kokmen, E ;
Petersen, RC .
NEUROLOGY, 1999, 53 (04) :795-800
[9]   Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia [J].
Boeve, BF ;
Lang, AE ;
Litvan, I .
ANNALS OF NEUROLOGY, 2003, 54 :S15-S19
[10]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259