DIFFUSE CORTICAL DYSPLASIA, OR THE DOUBLE CORTEX SYNDROME - THE CLINICAL AND EPILEPTIC SPECTRUM IN 10 PATIENTS

被引:181
作者
PALMINI, A
ANDERMANN, F
AICARDI, J
DULAC, O
CHAVES, F
PONSOT, G
PINARD, JM
GOUTIERES, F
LIVINGSTON, J
TAMPIERI, D
ANDERMANN, E
ROBITAILLE, Y
机构
[1] MONTREAL NEUROL HOSP & INST,3801 UNIV ST,MONTREAL H3A 2B4,QUEBEC,CANADA
[2] MCGILL UNIV,DEPT NEUROL & NEUROSURG,MONTREAL H3A 2T5,QUEBEC,CANADA
[3] HOP ST VINCENT DE PAUL,SERV NEUROL INFANTILE,F-75674 PARIS 14,FRANCE
[4] HOP ENFANTS MALAD,DEPT PEDIAT,PARIS,FRANCE
关键词
D O I
10.1212/WNL.41.10.1656
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Diffuse neuronal migration disorders associated with epilepsy can now be recognized by modem neuroimaging techniques, particularly high-resolution MRI. We report 10 patients with a recently described MRI picture of continuous or generalized band heterotopia underlying the cortical mantle, giving the appearance of a "double cortex." They have epilepsy, and almost all have mental retardation. The epileptic disorder varies in nature and degree of severity. Patients may present with infantile spasms, a Lennox-Gastaut syndrome, or other forms of secondary generalized or multifocal epilepsy. Response to medical treatment is variable. Callosotomy may lead to considerable reduction of drop attacks, present in 60%. Mental retardation is usually mild or moderate, and only rarely severe. It correlates with the type of epileptic syndrome, and is greater in patients with more disorganized cortex overlying the heterotopia. Recognition of this entity by MRI is important for appropriate diagnosis of the epileptic disorder, planning of therapeutic strategy, and prognosis.
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页码:1656 / 1662
页数:7
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