ELECTROCLINICAL SIGNIFICANCE OF ROLANDIC SPIKES AND DIPOLES IN NEURODEVELOPMENTALLY NORMAL-CHILDREN

被引:12
作者
LEGARDA, S [1 ]
JAYAKAR, P [1 ]
机构
[1] MIAMI CHILDRENS HOSP,CTR COMPREHENS EPILEPSY,MIAMI,FL
来源
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY | 1995年 / 95卷 / 04期
关键词
ROLANDIC SPIKES; CENTROTEMPORAL SPIKES; DIPOLES; ROLANDIC EPILEPSY; PEDIATRIC EPILEPSY; IDIOPATHIC EPILEPSY; CHILDREN;
D O I
10.1016/0013-4694(95)00108-B
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
''Centrotemporal'' (rolandic) spikes are elemental to the diagnosis of benign rolandic epilepsy (BRE) and may reveal a characteristic dipole distribution. Yet, not all children with rolandic spikes present with clinical seizures. Using additional scalp coverage according to the 10-10 electrode system, we attempted to correlate 2 specific spike features: (a) dipole fields, and (b) exact location of maximum negativity, with the presence or absence of clinical seizures in 42 neurodevelopmentally normal children with rolandic (central) spikes. Thirty-three (79%) presented with seizures. Seventeen of 21 children revealing dipoles (81%) and 16 of 21 patients without dipoles (74%) had seizures. Children with high central (C3/C4) foci were just as likely to present with seizures (10 of 15, 67%) as were those with low central (C5/C6) foci (23 of 27, 85%) (P > 0.10). The majority of our study subjects (27 of 42, 64%) revealed maximum negativity in the low central region (C5/C6), and the dipole feature was as likely to be associated with high central foci (7 of 15, 47%) as with low central foci (14 of 27, 52%). Although rolandic spikes are a reliable indicator of potential epileptogenicity, neither their exact location nor dipolar distribution help to further define the population with clinical seizures.
引用
收藏
页码:257 / 259
页数:3
相关论文
共 9 条
[1]   LONGITUDINAL-STUDY OF EPILEPTIFORM EEG PATTERNS IN NORMAL-CHILDREN [J].
CAVAZZUTI, GB ;
CAPPELLA, L ;
NALIN, A .
EPILEPSIA, 1980, 21 (01) :43-55
[2]  
GREGORY DL, 1991, EPILEPSIA, V33, P36
[3]   DIPOLE REVERSAL - AN ICTAL FEATURE OF BENIGN PARTIAL EPILEPSY WITH CENTROTEMPORAL SPIKES [J].
GUTIERREZ, AR ;
BRICK, JF ;
BODENSTEINER, J .
EPILEPSIA, 1990, 31 (05) :544-548
[4]   LOCALIZATION OF EPILEPTOGENIC FOCI USING A SIMPLE REFERENCE-SUBTRACTION MONTAGE TO DOCUMENT SMALL INTERCHANNEL TIME DIFFERENCES [J].
JAYAKAR, P ;
DUCHOWNY, MS ;
RESNICK, TJ ;
ALVAREZ, LA .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1991, 8 (02) :212-215
[5]   BENIGN ROLANDIC EPILEPSY - HIGH CENTRAL AND LOW CENTRAL SUBGROUPS [J].
LEGARDA, S ;
JAYAKAR, P ;
DUCHOWNY, M ;
ALVAREZ, L ;
RESNICK, T .
EPILEPSIA, 1994, 35 (06) :1125-1129
[6]  
LEGARDA S, 1994, ELECTROEN CLIN NEURO, V91, pP45
[7]  
LOISEAU P, 1989, CLEVELAND CLIN J S1, V56, P17
[8]   SEQUENTIAL EEG MAPPING MAY DIFFERENTIATE EPILEPTIC FROM NONEPILEPTIC ROLANDIC SPIKES [J].
VANDERMEIJ, W ;
VANHUFFELEN, AC ;
WIENEKE, GH ;
WILLEMSE, J .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1992, 82 (06) :408-414
[9]  
1990, MODIFIED NOMENCLATUR