Malformations of cortical development and epilepsy: A cohort of 150 patients in western China

被引:7
作者
Liu, Wenyu [1 ]
An, Dongmei [1 ]
Xiao, Jiahe [2 ]
Li, Jinmei [1 ]
Hao, Nanya [1 ]
Zhou, Dong [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Neurol, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Radiol, Chengdu 610041, Peoples R China
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2015年 / 32卷
关键词
Epilepsy; Malformations of cortical development; MRI; PERIVENTRICULAR NODULAR HETEROTOPIA; GENETIC CLASSIFICATION; CLINICAL-FEATURES; CORPUS-CALLOSUM; DYSPLASIA; CHILDREN; SPECTRUM; OUTCOMES; SURGERY; MEG;
D O I
10.1016/j.seizure.2015.09.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Malformations of cortical development (MCDs) are abnormalities of the cerebral cortex that arise from abnormal formation of the cortical plate, and have become increasingly identified as an important etiology for refractory epilepsy. Little is known about the spectrum, distribution and clinical features of MCDs, especially in resource-limited regions. This study investigates the distribution of MCDs and compares the clinical features and long-term prognosis between the two forms of MCDs: Simple and Multiple. Method: One hundred and fifty epilepsy patients (138 adults, 12 pediatric patients) with radiologically diagnosed MCDs were identified at a tertiary epilepsy center in western China. Patients were divided into three subtypes according to the Barkovich classification. They were further divided into either Simple or Multiple MCD forms based on whether they had a single type of MCDs or other co-existing developmental brain abnormalities. Results: The most common type of MCD is focal cortical dysplasia. We found perinatal insults more common in group III patients. Multiple MCD was identified in 36 of 150 patients, and was associated with higher rates of delayed milestones (p = 0.005), cognitive impairment (p = 0.023) and neurological deficits (p = 0.002) compared to Simple MCD. Extra-temporal epilepsy was more commonly seen among individuals with Multiple MCD (p = 0.017). Participants with Multiple MCD were younger at time of seizure onset (p = 0.003) and at assessment (p = 0.002), had a lower seizure-free rate (p = 0.033) and had worse outcomes overall. Patients with heterotopias were more commonly associated with other abnormalities. Conclusion: MCDs are a critical cause of epilepsy and pose a big challenge for resource-limited countries. Imaging techniques are crucial in diagnosing and classifying cortical deformities. Multiple malformations lead to more severe clinical features and worse prognosis. Identifying and classifying MCDs can help physicians to better estimate patient prognosis and seek the best, individualized therapeutic options. (C) 2015 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:92 / 99
页数:8
相关论文
共 36 条
[1]   Clinical, EEG, MRI, MEG, and surgical outcomes of pediatric epilepsy with astrocytic inclusions versus focal cortical dysplasia [J].
Alshafai, Laila ;
Ochi, Ayako ;
Go, Cristina ;
McCoy, Blathnaid ;
Hawkins, Cynthia ;
Otsubo, Hiroshi ;
Snead, Orlando C. ;
Rutka, James ;
Widjaja, Elysa .
EPILEPSIA, 2014, 55 (10) :1568-1575
[2]   PROPOSAL FOR REVISED CLASSIFICATION OF EPILEPSIES AND EPILEPTIC SYNDROMES [J].
不详 .
EPILEPSIA, 1989, 30 (04) :389-399
[3]   A developmental and genetic classification for malformations of cortical development: update 2012 [J].
Barkovich, A. James ;
Guerrini, Renzo ;
Kuzniecky, Ruben I. ;
Jackson, Graeme D. ;
Dobyns, William B. .
BRAIN, 2012, 135 :1348-1369
[4]   A developmental and genetic classification for malformations of cortical development [J].
Barkovich, AJ ;
Kuzniecky, RI ;
Jackson, GD ;
Guerrini, R ;
Dobyns, WB .
NEUROLOGY, 2005, 65 (12) :1873-1887
[5]   Combined EEG and MEG analysis of early somatosensory evoked activity in children and adolescents with focal epilepsies [J].
Bast, T. ;
Wright, T. ;
Boor, R. ;
Harting, I. ;
Feneberg, R. ;
Rupp, A. ;
Hoechstetter, K. ;
Rating, D. ;
Baumgaertner, U. .
CLINICAL NEUROPHYSIOLOGY, 2007, 118 (08) :1721-1735
[6]   Small focal cortical dysplasia lesions are located at the bottom of a deep sulcus [J].
Besson, Pierre ;
Andermann, Frederick ;
Dubeau, Francois ;
Bernasconi, Andrea .
BRAIN, 2008, 131 :3246-3255
[7]   The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission [J].
Bluemcke, Ingmar ;
Thom, Maria ;
Aronica, Eleonora ;
Armstrong, Dawna D. ;
Vinters, Harry V. ;
Palmini, Andre ;
Jacques, Thomas S. ;
Avanzini, Giuliano ;
Barkovich, A. James ;
Battaglia, Giorgio ;
Becker, Albert ;
Cepeda, Carlos ;
Cendes, Fernando ;
Colombo, Nadia ;
Crino, Peter ;
Cross, J. Helen ;
Delalande, Olivier ;
Dubeau, Francois ;
Duncan, John ;
Guerrini, Renzo ;
Kahane, Philippe ;
Mathern, Gary ;
Najm, Imad ;
Ozkara, Cigdem ;
Raybaud, Charles ;
Represa, Alfonso ;
Roper, Steven N. ;
Salamon, Noriko ;
Schulze-Bonhage, Andreas ;
Tassi, Laura ;
Vezzani, Annamaria ;
Spreafico, Roberto .
EPILEPSIA, 2011, 52 (01) :158-174
[8]   Type II focal cortical dysplasia: Electroclinical phenotype and surgical outcome related to imaging [J].
Chassoux, Francine ;
Landre, Elisabeth ;
Mellerio, Charles ;
Turak, Baris ;
Mann, Michael W. ;
Daumas-Duport, Catherine ;
Chiron, Catherine ;
Devaux, Bertrand .
EPILEPSIA, 2012, 53 (02) :349-358
[9]  
Colombo N, 2003, AM J NEURORADIOL, V24, P724
[10]  
Consalvo DE, 2006, MEDICINA-BUENOS AIRE, V66, P101