Frontotemporal lobar degeneration - A consensus on clinical diagnostic criteria

被引:4085
作者
Neary, D
Snowden, JS
Gustafson, L
Passant, U
Stuss, D
Black, S
Freedman, M
Kertesz, A
Robert, PH
Albert, M
Boone, K
Miller, BL
Cummings, J
Benson, DF
机构
[1] Manchester Royal Infirm, Dept Neurol, Manchester M13 9WL, Lancs, England
[2] Univ Lund Hosp, Lund, Sweden
[3] Baycrest Ctr Geriatr Care, Rotman Res Inst, Toronto, ON, Canada
[4] Univ Toronto, Toronto, ON, Canada
[5] Univ Western Ontario, London, ON, Canada
[6] Univ Nice, Sch Med, F-06108 Nice 2, France
[7] Massachusetts Gen Hosp, Boston, MA 02114 USA
[8] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90024 USA
基金
英国惠康基金;
关键词
D O I
10.1212/WNL.51.6.1546
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To improve clinical recognition and provide research diagnostic criteria for three clinical syndromes associated with frontotemporal lobar degeneration. Methods: Consensus criteria for the three prototypic syndromes-frontotemporal dementia, progressive nonfluent aphasia, and semantic dementia-were developed by members of an international workshop on frontotemporal lobar degeneration. These criteria build on earlier published clinical diagnostic guidelines for frontotemporal dementia produced by some of the workshop members. Results: The consensus criteria specify core and supportive features for each of the three prototypic clinical syndromes and provide broad inclusion and exclusion criteria for the generic entity of frontotemporal lobar degeneration. The criteria are presented in lists, and operational definitions for features are provided in the text. Conclusions: The criteria ought to provide the foundation for research work into the neuropsychology, neuropathology, genetics, molecular biology, and epidemiology of these important clinical disorders that account for a substantial proportion of cases of primary degenerative dementia occurring before the age of 65 years.
引用
收藏
页码:1546 / 1554
页数:9
相关论文
共 48 条
[1]  
ASSAL G, 1985, REV NEUROL, V141, P245
[2]   PROGRESSIVE LANGUAGE IMPAIRMENT WITHOUT DEMENTIA - A CASE WITH ISOLATED CATEGORY SPECIFIC SEMANTIC DEFECT [J].
BASSO, A ;
CAPITANI, E ;
LAIACONA, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1988, 51 (09) :1201-1207
[3]  
BRION S, 1980, Encephale, V6, P259
[4]   FAMILIAL NONSPECIFIC DEMENTIA MAPS TO CHROMOSOME-3 [J].
BROWN, J ;
ASHWORTH, A ;
GYDESEN, S ;
SORENSEN, A ;
ROSSOR, M ;
HARDY, J ;
COLLINGE, J .
HUMAN MOLECULAR GENETICS, 1995, 4 (09) :1625-1628
[5]  
BRUN A, 1994, J NEUROL NEUROSUR PS, V57, P416
[7]   FRONTAL-LOBE DEGENERATION OF NON-ALZHEIMER TYPE REVISITED [J].
BRUN, A .
DEMENTIA, 1993, 4 (3-4) :126-131
[8]   RAPIDLY PROGRESSIVE APHASIC DEMENTIA AND MOTOR-NEURON DISEASE [J].
CASELLI, RJ ;
WINDEBANK, AJ ;
PETERSEN, RC ;
KOMORI, T ;
PARISI, JE ;
OKAZAKI, H ;
KOKMEN, E ;
IVERSON, R ;
DINAPOLI, RP ;
GRAFFRADFORD, NR ;
STEIN, SD .
ANNALS OF NEUROLOGY, 1993, 33 (02) :200-207
[9]   SLOWLY PROGRESSIVE APHASIA WITHOUT GENERALIZED DEMENTIA - STUDIES WITH POSITRON EMISSION TOMOGRAPHY [J].
CHAWLUK, JB ;
MESULAM, MM ;
HURTIG, H ;
KUSHNER, M ;
WEINTRAUB, S ;
SAYKIN, A ;
RUBIN, N ;
ALAVI, A ;
REIVICH, M .
ANNALS OF NEUROLOGY, 1986, 19 (01) :68-74
[10]  
CONSTANTINIDIS J, 1987, Encephale, V13, P285