Microdysgenesis with abnormal cortical myelinated fibres in temporal lobe epilepsy: a histopathological study with calbindin D-28-K immunohistochemistry

被引:38
作者
Thom, M
Holton, JL
D'Arrigo, C
Griffin, B
Beckett, A
Sisodiya, S
Alexiou, D
Sander, JW
机构
[1] UCL, Inst Neurol, Dept Neuropathol, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Dept Neuropathol, London WC1N 3BG, England
[3] Natl Hosp Neurol & Neurosurg, Dept Neurol, London WC1N 3BG, England
关键词
calbindin; epilepsy; microdysgenesis; myelinated fibres;
D O I
10.1046/j.1365-2990.2000.00229.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Microdysgenesis is a microscopic cortical malformation reported to occur with varying incidence in surgical lobectomies from patients with temporal lobe epilepsy (TLE). It may act as a substrate for the seizures. Four patients are reported with TLE, hippocampal sclerosis and cortical microdysgenesis which was also characterized by the presence of abnormal myelinated fibres running tangentially in the superficial cortical laminae and closely associated with abnormal clusters of neurones. Similar abnormal cortical fibres have been described in other malformations of cortical development including polymicrogyria and focal cortical dysplasia and it is therefore likely that these fibres represent part of the microdysgenetic malformation not hitherto reported. The possibility is discussed that they may also be of functional significance in terms of influencing local seizure propagation and the secondary cortical neuronal loss observed, predominantly affecting layer II. Studies of calbindin interneuronal populations showed preservation of these cells in the microdysgenetic cortex, when compared with non-malformed temporal lobes, despite an overall reduction in cortical neuronal density. In addition, prominent numbers of neurogliaform calbindin-positive nerve cells were observed in the microdysgenesis cases and the nature of these cells is speculated upon.
引用
收藏
页码:251 / 257
页数:7
相关论文
共 20 条
[1]  
ARMSTRONG D, 1993, J NEUROPATHOL EXP NE, V52, P443
[2]  
Cavanagh JB, 1956, BRIT MED J, P1403
[3]   LOCAL CIRCUIT NEURONS IMMUNOREACTIVE FOR CALRETININ, CALBINDIN D-28K OR PARVALBUMIN IN MONKEY PREFRONTAL CORTEX - DISTRIBUTION AND MORPHOLOGY [J].
CONDE, F ;
LUND, JS ;
JACOBOWITZ, DM ;
BAIMBRIDGE, KG ;
LEWIS, DA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 341 (01) :95-116
[4]   CALBINDIN IMMUNOREACTIVITY IN NORMAL HUMAN TEMPORAL NEOCORTEX [J].
FERRER, I ;
TUNON, T ;
SORIANO, E ;
DELRIO, A ;
IRAIZOZ, I ;
FONSECA, M ;
GUIONNET, N .
BRAIN RESEARCH, 1992, 572 (1-2) :33-41
[5]   ABNORMAL LOCAL-CIRCUIT NEURONS IN EPILEPSIA PARTIALIS CONTINUA ASSOCIATED WITH FOCAL CORTICAL DYSPLASIA [J].
FERRER, I ;
PINEDA, M ;
TALLADA, M ;
OLIVER, B ;
RUSSI, A ;
OLLER, L ;
NOBOA, R ;
ZUJAR, MJ ;
ALCANTARA, S .
ACTA NEUROPATHOLOGICA, 1992, 83 (06) :647-652
[6]   PARVALBUMIN AND CALBINDIN-D28K IMMUNOCYTOCHEMISTRY IN HUMAN NEOCORTICAL EPILEPTIC FOCI [J].
FERRER, I ;
OLIVER, A ;
RUSSI, R ;
CASAS, R ;
RIVERA, R .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 123 (1-2) :18-25
[7]  
FRIEDE RL, 1989, DEV NEUROPATHOLOGY, P331
[8]  
HARDIN B, 1997, GREENFIELDS NEUROPAT, V1, P397
[9]  
Janota I, 1992, RECENT ADV EPILEPSY, P37
[10]   Temporal lobe microdysgenesis in epilepsy versus control brains [J].
Kasper, BS ;
Stefan, H ;
Buchfelder, M ;
Paulus, W .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1999, 58 (01) :22-28