Giant visually-evoked potentials without myoclonus in the Heidenhain type of Creutzfeld-Jakob disease

被引:12
作者
Finsterer, J
Bancher, C
Mamoli, B
机构
[1] NKH Rosenhugel, Ludwig Boltzmann Inst Res Epilepsy & Neuromuscula, Vienna, Austria
[2] Municipal Hosp Lainz, Dept Neurol, Vienna, Austria
关键词
spongiform encephalopathy; prion disease; visually-evoked potentials; impaired visual acuity;
D O I
10.1016/S0022-510X(99)00145-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In a 64-year old woman with progressive visual impairment for 4 weeks, probable Creutzfeld-Jakob disease without myoclonus was diagnosed after rapidly progressive mental deterioration had also developed, and CSF and EEG showed characteristic findings. Pattern-reversal and flash visually-evoked potentials, recorded 5, 6, 7 and 8 weeks after onset, showed a maximum P100 latency of 210 ms, 8 weeks after onset, and a maximum N75/P100 amplitude of 33.1 mu V, 5 weeks after onset. While the P100 latency progressively increased, the N75/P100 amplitude continuously decreased after reaching its maximum. In the Heidenhain type of Creutzfeld-Jakob disease giant visually-evoked potentials may be recorded during the early stages of the disease, even in the absence of myoclonus. Visually-evoked potentials may prove useful in diagnosing Creutzfeld-Jakob disease with atypical initial presentation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 75
页数:3
相关论文
共 13 条
[1]   SENSORY EVOKED-POTENTIALS IN CREUTZFELDT-JAKOB DISEASE [J].
AGUGLIA, U ;
FARNARIER, G ;
REGIS, H ;
OLIVERI, RL ;
QUATTRONE, A .
EUROPEAN NEUROLOGY, 1990, 30 (03) :157-161
[2]   HUMAN SPONGIFORM ENCEPHALOPATHY - THE NATIONAL-INSTITUTES-OF-HEALTH SERIES OF 300 CASES OF EXPERIMENTALLY TRANSMITTED DISEASE [J].
BROWN, P ;
GIBBS, CJ ;
RODGERSJOHNSON, P ;
ASHER, DM ;
SULIMA, MP ;
BACOTE, A ;
GOLDFARB, LG ;
GAJDUSEK, DC .
ANNALS OF NEUROLOGY, 1994, 35 (05) :513-529
[3]  
Budka H, 1998, WIEN KLIN WOCHENSCHR, V110, P451
[4]   Creutzfeldt-Jakob disease -: Neurophysiologic visual impairments [J].
de Seze, J ;
Hache, JC ;
Vermersch, P ;
Arndt, CF ;
Maurage, CA ;
Pasquier, F ;
Laplanche, JL ;
Ruchoux, MM ;
Leys, D ;
Destée, A ;
Petit, H .
NEUROLOGY, 1998, 51 (04) :962-967
[5]   PERIODIC SYNCHRONOUS DISCHARGES AND VISUAL-EVOKED POTENTIALS IN CREUTZFELDT-JAKOB-DISEASE - PSD-TRIGGERED FLASH VEPS [J].
FUKUI, R ;
TOBIMATSU, S ;
KATO, M .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1994, 90 (06) :433-437
[6]   Diagnostic criteria for sporadic Creutzfeldt-Jakob disease [J].
Kretzschmar, HA ;
Ironside, JW ;
DeArmond, SJ ;
Tateishi, J .
ARCHIVES OF NEUROLOGY, 1996, 53 (09) :913-920
[7]   CREUTZFELDT-JAKOB DISEASE AND OPTIC ATROPHY [J].
LESSER, RL ;
ALBERT, DM ;
BOBOWICK, AR ;
OBRIEN, FH .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1979, 87 (03) :317-321
[8]   Neuro-ophthalmological aspects of prion diseases [J].
Neetens, A ;
Martin, JJ .
NEURO-OPHTHALMOLOGY, 1998, 19 (03) :137-144
[9]   Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease [J].
Otto, M ;
Wiltfang, J ;
Tumani, H ;
Zerr, I ;
Lantsch, M ;
Kornhuber, J ;
Weber, T ;
Kretzschmar, HA ;
Poser, S .
NEUROSCIENCE LETTERS, 1997, 225 (03) :210-212
[10]  
Radbauer C, 1998, WIEN KLIN WOCHENSCHR, V110, P496