Source localization and possible causes of interictal epileptic activity in tumor-associated epilepsy

被引:44
作者
Patt, S [1 ]
Steenbeck, J
Hochstetter, A
Kraft, R
Huonker, R
Haueisen, J
Haberland, N
Ebmeier, T
Hliscs, R
Fiehler, J
Nowak, H
Kalff, R
机构
[1] Univ Jena, Inst Pathol Neuropathol, D-07740 Jena, Germany
[2] Univ Jena, Clin Neurosurg, D-07740 Jena, Germany
[3] Univ Jena, Neurol Clin, D-07740 Jena, Germany
[4] Univ Jena, Biomagnet Ctr, D-07740 Jena, Germany
关键词
brain tumors; dipole source localization; epilepsy; MEG; patch-clamp; voltage-gated sodium channels;
D O I
10.1006/nbdi.2000.0288
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Electrophysiological studies in gliomas have demonstrated action potentials in neoplastic cells. These "spiking tumor cells" are, however, an enigma. In attempt to find evidences for spikes within tumoral borders, 21 patients with different intracerebral tumors were preoperatively screened for the occurrence of epileptogenic discharges using multichannel MEG and EEG. A correlation between histopathology and the distance between dipole and tumor border could be found. Glioma patients showed epileptic activities closer to the border than those with mixed glioneuronal neoplasms and metastases. Four glioma patients demonstrated epileptic activity within the tumor boundary, however, not in the deep center of the tumor. Patch-clamping of cells from acute glioma slices did not yield a correlation between the presence of voltage-gated sodium channels in tumor cells and the MEG/EEG data. Our results demonstrate that the zone with the highest epileptogenic potential is different in gliomas and other brain tumors. However, our data do not strongly suggest that glioma cells are directly involved in the generation of tumor-associated epilepsy in vivo via their capability to generate action potentials. (C) 2000 Academic Press.
引用
收藏
页码:260 / 269
页数:10
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