Surgical resection of focal cortical dysplasias in the central region

被引:17
作者
Marnet, D. [1 ]
Devaux, B. [1 ]
Chassoux, F. [1 ]
Landre, E. [1 ]
Mann, M. [1 ]
Turak, B. [1 ]
Rodrigo, S. [2 ]
Varlet, P. [3 ]
Daumas-Duport, C. [3 ]
机构
[1] Univ Paris 05, Ctr Hosp St Anne, Serv Neurochirurg, F-75674 Paris 14, France
[2] Univ Paris 05, Ctr Hosp St Anne, Serv Imagerie Morphol & Fonct, F-75674 Paris, France
[3] Univ Paris 05, Ctr Hosp St Anne, Serv Anat Pathol, F-75674 Paris, France
关键词
epilepsy; sensorimotor region; cortical dysplasias; epilepsy surgery;
D O I
10.1016/j.neuchi.2008.02.054
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose. - Taylor-type focal cortical dysplasias (TTFCD) represent a particular pathological entity responsible for severe drug-resistant epilepsy of extratemporal location. Epilepsy can be surgically cured if complete removal of the lesion can be performed. However, identification on imaging may be difficult and negative standard MRIs are not rare. The frequent location of TTFCD in the central region restrains the possibilities of complete resection. We report a series of patients operated on for intractable epilepsy associated with TTFCD in the central area. Patients and methods. - Between 2000 and 2006, of 34 consecutive patients with TTFCD, 17 had a lesion located in the central area. MRI was considered normal in eight, although in five a subtle gyral abnormality was disclosed on further analysis. A (18)FDG PET scan performed in 16 cases demonstrated focal hypometabolism in 15 that correlated with abnormalities on MRI when visible. SEEG performed in 13 cases revealed typical abnormalities for TTFCD in 10 cases. At resection, cortical and subcortical stimulations of the dysplastic cortex did not elicit a motor response. Results. - Postoperative motor or sensory deficit was observed in 13 patients - severe in four - which subsequently resolved completely in seven. Six patients had a minor permanent, motor or sensory deficit. Four patients were reoperated for seizure recurrence and residual dysplastic tissue was found at reoperation in three cases. Average postoperative follow-up was 3.7 years. Sixteen patients (94%) were in Engel Class I (65% in Class IA). Conclusion. - This study suggests that surgical resection of central region TTFCD may be associated with favorable seizure outcome and no or minor functional permanent disability. In cases of seizure relapse, reoperation can be performed without further permanent deficit and lead to seizure-free outcome. Future techniques for intraoperative detection of these lesions could optimize their complete resection in functional areas. (c) 2008 Publie par Elsevier Masson SAS.
引用
收藏
页码:399 / 408
页数:10
相关论文
共 57 条
[1]   Complex central cortex in pediatric patients with malformations of cortical development [J].
Akai, T ;
Otsubo, H ;
Pang, EW ;
Rutka, JT ;
Chitoku, S ;
Weiss, SK ;
Snead, OC .
JOURNAL OF CHILD NEUROLOGY, 2002, 17 (05) :347-352
[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]  
Avoli M, 1999, ANN NEUROL, V46, P816, DOI 10.1002/1531-8249(199912)46:6<816::AID-ANA3>3.0.CO
[4]  
2-O
[5]  
Bach-Y-Rita Paul, 2005, Journal of Integrative Neuroscience, V4, P183, DOI 10.1142/S0219635205000768
[6]   Neuroimaging of focal malformations of cortical development [J].
Barkovich, AJ ;
Kuzniecky, RI .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1996, 13 (06) :481-494
[7]   Classification system for malformations of cortical development - Update 2001 [J].
Barkovich, AJ ;
Kuzniecky, RI ;
Jackson, GD ;
Guerrini, R ;
Dobyns, WB .
NEUROLOGY, 2001, 57 (12) :2168-2178
[8]   Focal cortical dysplasia: prevalence, clinical presentation and epilepsy in children and adults [J].
Bast, T ;
Ramantani, G ;
Seitz, A ;
Rating, D .
ACTA NEUROLOGICA SCANDINAVICA, 2006, 113 (02) :72-81
[9]  
Bastos AC, 1999, ANN NEUROL, V46, P88, DOI 10.1002/1531-8249(199907)46:1<88::AID-ANA13>3.0.CO
[10]  
2-4