Table 2.
Pat. no. | Sex/age | Age at debut | Semiology | Surface EEG ictal epileptiform discharges | Surface EEG interictal epileptiform discharges | ECOG | MEG | FDG PET | SPECT | 1.5 T MRI | 3 T MRI | 7 T MRI | Surgery | Histopathology (ILEA type) | Outcome (Engel Score) |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | ♀/44 | 26 | Focal impaired awareness seizures; hyperkinetic seizures | R frontal parasagittal | R frontal parasagittal | Continuous spiking, R frontal parasagittal | Not performed | No abnormalities | Not performed | Not performed | No abnormalities | Subtle blurring, hyperintensity on DIR R frontal parasagittal | R Partial lobectomy frontal parasagittal | FCD IIb | 1A+ 5 years |
2 | ♂/7 | 4 | Focal impaired awareness seizures, R hand automatisms | R frontal | R frontal parasagittal | Continuous spiking R frontal parasagittal | Not performed | No abnormalities | Not performed | Not performed | No abnormalities | R frontal small area with subtle blurring of G/W boundary, subtle white matter hyperintensity (T2) | R frontal lesionectomy | FCD IIa | 1A+ ½ year |
3 | ♀/40 | 24 | Focal impaired awareness seizures, dysphasia and alexia; focal to bilateral tonic‐clonic seizures | L temporal | L temporal | Interictal diffuse L temporal, ictal neocortical L mid‐temporal | Spikes neocortex L medial temporal gyrus | No abnormalities | Not performed | No abnormalities a | No abnormalities | Subcortical hyperintensities (FLAIR + T2), blurring of GW‐junction L anterior superior temporal gyrus | Lesionectomy L medial temporal gyrus | mMCD with oligodendroglial hyperplasia | 1A+ 1 year |
4 | ♀/22 | 8 | Focal impaired awareness seizures; visual aura; focal to bilateral tonic‐clonic seizures | Onset mid‐frontal | Mid‐frontal | Not performed | Multifocal, at distance from visual cortex | L Occipital hypermetabolism | Not performed | No abnormalities | No abnormalities | Subtle white matter signal changes, transmantle sign‐like configuration L inferior occipital gyrus. | Under evaluation | n/a | n/a |
5 | ♂/21 | 15 | Focal impaired awareness seizures, stops activity, staring, L‐sided version, automatisms | L frontal | L frontal | Continuous spiking L medial frontal gyrus | L frontal epileptic activity | L temporal hypometabolism | L frontal (consistent with 7 T MRI) and less pronounced L parietal | Not performed | No abnormalities a | L frontal operculum/inferior frontal sulcus abnormal gyration and subtle transmantle hyperintensity (WMS), enhanced venous vasculature in sulcus (T2*) | Corticectomy L medial frontal gyrus | mMCD type 2, sample error likely, no examination of center of MRI lesion | 1A+ 4 months |
6 | ♂/14 | 4 | Focal impaired awareness seizures, hyperkinetic | L frontal | Ictal onset L frontal | Continuous spiking depth of L superior frontal sulcus (depth electrode) | L frontal spikes | No seizure focus | Not performed | No abnormalities a | No abnormalities | L frontal abnormally deep sulcus with blurring GM‐junction, cortical thickening and subtle transmantle sign | Lesionectomy L middle frontal gyrus | FCD IIb | 1A+ 1½ months |
7 | ♂/14 | 10 | Focal impaired awareness seizures, nocturnal seizures with automatisms; bilateral tonic‐clonic seizures | Not performed | L centro‐parietal | Not performed | L parietal epileptic activity | L parietal hypometabolism | Not performed | Not performed | No abnormalities | L parietal radial band of poorly demarcated white matter signal changes | Lesionectomy with ACOG planned | n/a | n/a |
8 | ♀/28 | 15 | Focal impaired awareness seizures, arrest of activity; focal to bilateral tonic‐clonic seizures | L temporal | Bilateral fronto‐centro‐temporal | Planned | Not performed | L temporo‐parietal, angular gyrus hypometabolism | Not performed | No abnormalities a | No abnormalities a | Abnormal intraparenchymal venous pattern posterior L medial temporal gyrus. | Grid planned | n/a | n/a |
9 | ♂/15 | 11 | Focal impaired awareness seizures, L‐sided head version, irresponsiveness, dysphasia, amnesia; focal to bilateral tonic‐clonic seizures | Non‐lateralizing | Multifocal | Diffuse L temporo‐parietal | L baso‐temporal, up to posterior temporal | No abnormalities | Not performed | MTS L + dubious blurring GWM‐junction and decreased volume L temporal | MTS L + dubious blurring GWM‐junction and decreased volume L temporal a | MTS L + abnormal gyration L anterior temporal and enhanced venous vasculature (T2*) | NVS after initial grid registration. Ultimately selective L anterior lobectomy + hippocampectomy | mMCD type 2, no MTS | 4B+ ½ year |
10 | ♀/28 | 0 | Focal impaired awareness seizures, automatisms, expressive dysphasia | L mid‐temporal sharp waves | L mid‐temporal spikes | L anterior temporal neocortical + hippocampus | Not performed | L temporal hypometabolism | Not performed | Possible MTS L | MTS L + unclear demarcation of GWM‐junction temporal lobe | MTS L + unclear demarcation of GWM‐junction temporal lobe. No indication of dual pathology | L anterior temporal lobectomy + amygdalahi pocampectomy | MTS ILAE class 2 + FCD IIIa | 1A− 1 year |
11 | ♀/15 | 9 | Focal aware seizures, R‐sided version eyes/head; bilateral tonic‐clonic seizures | L fronto‐central | No distinct epileptiform activity | Ictal onset L fronto‐central | L fronto‐central spikes | No abnormalities | Not performed | No abnormalities | No abnormalities | No abnormalities | Lesionectomy L pre‐central, pre‐central sulcus | Normal tissue (suspect for sample error, FCD in bottom of sulcus) | 1A− 2 years |
12 | ♂/14 | 7 | Focal impaired awareness seizures, left tonic; focal to bilateral tonic‐clonic seizures | R fronto‐central | R posterior temporal | Continuous spiking R baso‐ temporo‐occipital | R temporal spikes | R baso‐temporo‐occipital hypo‐metabolism | Not performed | No abnormalities a | No abnormalities | No abnormalities (severe signal loss in temporal lobes) | R baso‐temporo‐occipital lesionectomy | FCD IIa | 1A− 1 year |
13 | ♂/18 | 14 | Focal impaired awareness seizures hyperkinetic; focal to bilateral tonic‐clonic seizures | No distinct epileptiform activity | No distinct epileptiform activity | No interictal activity, ictal medial frontal gyrus | No abnormalities | R frontal hypometabolism | Not performed | No abnormalities a | Not performed | No abnormalities | Corticectomy R medial frontal gyrus | mMCD type 2 | 1D+ 5 year |
14 | ♀/22 | 11 | Focal impaired awareness seizures, sensory dysphasia, derealization, sensations in left foot; focal to bilateral tonic‐clonic seizures | R posterior baso‐temporal | R posterior temporal | Bursts R posterior temporal, sporadic spikes R hippocampus | R hemisphere, no clear localization | Dubious hypometabolism R operculum | Not performed | Not performed | No abnormalities | No abnormalities | Resection posterior baso‐temporal, fusiform gyrus | Normal, but suboptimal assessment due to fragmentation | 1A+ 1/2 year |
15 | ♂/33 | 20 | Focal impaired awareness seizures, auditory phenomena, R‐sided head version, confusion; focal to bilateral tonic‐clonic seizures | L posterior temporal | Aspecific irregularities bilateral fronto‐temporal | Sporadic spikes L lateral temporal | Not conclusive | L baso‐temporal‐parietal, hypometabolism in large area | Not performed | Not performed | No abnormalitiesa | No abnormalities | Corticectomy L superior and middle temporal gyrus | No abnormalities | 1A+ 1 month |
16 | ♂/16 | 12 | Focal impaired awareness seizures, myoclonia all extremities, L‐sided version of eyes followed by diminished vision; bilateral tonic‐clonic seizures | R temporo‐occipital | R temporo‐occipital | Continuous spikes R lateral temporal, sporadic spikes R parietal and lateral and medial temporal | Baso‐temporal/lateral and R posterior insula | R temporo‐occipital hypometabolism | Not performed | No abnormalitiesa | No abnormalities | No abnormalities | R temporal lobectomy | mMCD type 2 | Follows |
DIR, double inversion recovery sequence; ECOG, electrocorticography; EEG, electroencephalogram; Engel score: 1A, completely seizure free; 1D, only seizures after discontinuation of antiepileptic drugs; +, on antiepileptic drugs; −, antiepileptic drugs discontinued; FDG‐PET, fluorodeoxyglucose (18F) positron emission tomography; FLAIR, fluid‐attenuated inversion recovery sequence; GW‐junction, gray and white matter junction L, left‐sided; MEG, magnetoencephalogram; MTS, mesiotemporal sclerosis; R, right‐sided.
MRI scan performed outside University Medical Center Utrecht.