Local and remote epileptogenicity in focal cortical dysplasias and neurodevelopmental tumours

被引:131
作者
Aubert, Sandrine [1 ,2 ]
Wendling, Fabrice [3 ,4 ]
Regis, Jean [5 ]
McGonigal, Aileen [1 ,2 ]
Figarella-Branger, Dominique [6 ]
Peragut, Jean-Claude [5 ]
Girard, Nadine [7 ]
Chauvel, Patrick [1 ,2 ,8 ]
Bartolomei, Fabrice [1 ,2 ,8 ]
机构
[1] CHU Timone, Serv Neurophysiol Clin, F-13000 Marseille, France
[2] Univ Mediterranee, LNN, F-13000 Marseille, France
[3] INSERM, U642, F-35000 Rennes, France
[4] Univ Rennes 1, LTSI, F-35000 Rennes, France
[5] CHU Timone, Serv Neurochirurg Fonct, F-13000 Marseille, France
[6] CHU Timone, Serv Anatomopathol, F-13000 Marseille, France
[7] CHU Timone, Serv Neuroradiol, F-13000 Marseille, France
[8] INSERM, U751, F-13000 Marseille, France
关键词
partial epilepsy; rapid discharge; focal cortical dysplasia; intracerebral recordings; prognosis; DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMORS; TEMPORAL-LOBE EPILEPSY; NEURONAL MIGRATION DISORDERS; INTRACTABLE PARTIAL EPILEPSY; HIGH-FREQUENCY OSCILLATIONS; RESISTANT PARTIAL EPILEPSY; LONG-TERM SEIZURE; INTRINSIC EPILEPTOGENICITY; SURGICAL-TREATMENT; CLINICAL CORRELATIONS;
D O I
10.1093/brain/awp242
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
During the pre-surgical evaluation of drug-resistant epilepsy, the assessment of the extent of the epileptogenic zone and its organization is a crucial objective. Indeed, the epileptogenic zone may be organized as a simple focal lesional site or as a more complex network (often referred to as the 'epileptogenic network') extending beyond the lesion. This distinction is particularly relevant in developmental lesions such as focal cortical dysplasias or dysembryoplastic neuroepithelial tumours and may determine both the surgical strategy and the prognosis. In this study, we have quantified the epileptogenic characteristic of brain structures explored by depth electrodes in 36 patients investigated by stereoelectroencephalography and suffering from focal drug-resistant epilepsy associated with focal cortical dysplasias or dysembryoplastic neuroepithelial tumours. This quantification was performed using the 'Epileptogenicity Index' method that accounts for both the propensity of a brain area to generate rapid discharges and the time for this area to get involved in the seizure. Epileptogenicity Index values range from 0 (no epileptogenicity) to 1 (maximal epileptogenicity). We determined Epileptogenicity Index from signals recorded in distinct brain structures including the lesional site. We studied the type of epileptogenic zone organization (focal versus network) and looked for a correlation with clinical data and post-surgical outcome. Mean Epileptogenicity Index in lesional regions was 0.87 (+/- 0.25), and 0.29 (+/- 0.30) in 'non-lesional' structures. The number of highly epileptogenic structures (defined by Epileptogenicity Index value >= 0.4) was 3.14 (+/- 1.87) in the whole population. We found that 31% of patients had only one epileptogenic structure (N-EI >= 0.4 = 1), therefore disclosing a strictly focal epileptogenic zone organization while 25 patients had more than one epileptogenic region, disclosing a network (61%) or bilateral (8%) epileptogenic zone organization. We observed a trend for a difference in seizure outcome according to the type of epileptogenic zone organization. Indeed, 57% of patients with network organization and 87% with focal organization were seizure-free while none of those with bilateral organization became seizure-free. The determination of Epileptogenicity Index computed from electrophysiological signals recorded according to the stereoelectroencephalography technique is a novel tool. Results suggest that it can help in the delineation of the epileptogenic zone associated with brain lesions and that it could be used in the definition of the subsequent surgical resection.
引用
收藏
页码:3072 / 3086
页数:15
相关论文
共 101 条
[1]   POWER SPECTRUM AND INTRACRANIAL EEG PATTERNS AT SEIZURE ONSET IN PARTIAL EPILEPSY [J].
ALARCON, G ;
BINNIE, CD ;
ELWES, RDC ;
POLKEY, CE .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1995, 94 (05) :326-337
[2]   Is it worth pursuing surgery for epilepsy in patients with normal neuroimaging? [J].
Alarcón, G ;
Valentín, A ;
Watt, C ;
Selway, RP ;
Lacruz, ME ;
Elwes, RDC ;
Jarosz, JM ;
Honavar, M ;
Brunhuber, F ;
Mullatti, N ;
Bodi, I ;
Salinas, M ;
Binnie, CD ;
Polkey, CE .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2006, 77 (04) :474-480
[3]   VERY HIGH-FREQUENCY RHYTHMIC ACTIVITY DURING SEEG SUPPRESSION IN FRONTAL-LOBE EPILEPSY [J].
ALLEN, PJ ;
FISH, DR ;
SMITH, SJM .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1992, 82 (02) :155-159
[4]   Inhibitory networks in epilepsy-associated gangliogliomas and in the perilesional epileptic cortex [J].
Aronica, E. ;
Redeker, S. ;
Boer, K. ;
Spliet, W. G. M. ;
van Rijen, P. C. ;
Gorter, J. A. ;
Troost, D. .
EPILEPSY RESEARCH, 2007, 74 (01) :33-44
[5]   Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after surgery [J].
Aronica, E ;
Leenstra, S ;
van Veelen, CWM ;
van Rijen, PC ;
Hulsebos, TJ ;
Tersmette, AC ;
Yankaya, B ;
Troost, D .
EPILEPSY RESEARCH, 2001, 43 (03) :179-191
[6]  
BANCAUD J, 1970, ELECTROEN CLIN NEURO, V28, P85
[7]  
Bancaud J., 1965, la stereoencephalographic dans l-epilepsie
[8]   MR OF NEURONAL MIGRATION ANOMALIES [J].
BARKOVICH, AJ ;
CHUANG, SH ;
NORMAN, D .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1988, 150 (01) :179-187
[9]   Cortical stimulation study of the role of rhinal cortex in deja vu and reminiscence of memories [J].
Bartolomei, F ;
Barbeau, E ;
Gavaret, M ;
Guye, M ;
McGonigal, A ;
Régis, J ;
Chauvel, P .
NEUROLOGY, 2004, 63 (05) :858-864
[10]  
Bartolomei F., 2002, REV NEUROL PARIS, V158, P4555