TY - JOUR
T1 - Three-dimensional localization of subclinical ictal activity by magnetoencephalography
T2 - Correlation with invasive monitoring
AU - Ishibashi, Hideaki
AU - Morioka, Takato
AU - Shigeto, Hiroshi
AU - Nishio, Shunji
AU - Yamamoto, Tomoya
AU - Fukui, Masashi
N1 - Funding Information:
We thank Koichi Nitta, Kazumi Takahashi, and Yuko Somehara, Bio-Medical Division, Sumitomo Metal Ind., LTD, for their technical assistance. This work was supported by the Magnetic Health Science Foundation.
PY - 1998/8
Y1 - 1998/8
N2 - BACKGROUND Although magnetoencephalography (MEG) provides accurate information on the spatial distribution and temporal patterns of the 'interictal' epileptic activities, it is interictal in nature and therefore also prone to all the problems associated with interictal data. METHODS We investigated the subclinical 'ictal' epileptic activity with a 37-channel, large-array biomagnetometer and mapped the data onto a three-dimensional image in a patient with intractable frontal lobe epilepsy. Dipole source localization was calculated based on magnetic fields for both the interictal and subclinical ictal activities. RESULTS The current dipoles of the interictal MEG spikes (MEG irritative zone) were revealed to be scattered in the left anterior frontal lobe, whereas that of the subclinical ictal onset (MEG subclinical ictal onset zone) was surrounded by the interictal dipole cluster. The dipole source localization of the propagating activities was not calculated with a single dipole model. The MEG subclinical ictal onset zone correlated well with the ictal onset zone subsequently recorded by invasive subdural electrophysiological monitoring. After multiple subpial transection of the deduced epileptogenic area, a dramatic reduction of the seizures occurred. CONCLUSION These results illustrate the potential of MEG for localizing the epileptogenic foci with high spatial and temporal resolution.
AB - BACKGROUND Although magnetoencephalography (MEG) provides accurate information on the spatial distribution and temporal patterns of the 'interictal' epileptic activities, it is interictal in nature and therefore also prone to all the problems associated with interictal data. METHODS We investigated the subclinical 'ictal' epileptic activity with a 37-channel, large-array biomagnetometer and mapped the data onto a three-dimensional image in a patient with intractable frontal lobe epilepsy. Dipole source localization was calculated based on magnetic fields for both the interictal and subclinical ictal activities. RESULTS The current dipoles of the interictal MEG spikes (MEG irritative zone) were revealed to be scattered in the left anterior frontal lobe, whereas that of the subclinical ictal onset (MEG subclinical ictal onset zone) was surrounded by the interictal dipole cluster. The dipole source localization of the propagating activities was not calculated with a single dipole model. The MEG subclinical ictal onset zone correlated well with the ictal onset zone subsequently recorded by invasive subdural electrophysiological monitoring. After multiple subpial transection of the deduced epileptogenic area, a dramatic reduction of the seizures occurred. CONCLUSION These results illustrate the potential of MEG for localizing the epileptogenic foci with high spatial and temporal resolution.
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U2 - 10.1016/S0090-3019(97)00411-4
DO - 10.1016/S0090-3019(97)00411-4
M3 - Article
C2 - 9701121
AN - SCOPUS:0031854443
SN - 0090-3019
VL - 50
SP - 157
EP - 163
JO - Surgical Neurology
JF - Surgical Neurology
IS - 2
ER -