Objectives: To investigate the use of whole brain voxel based morphometry (VBM) and stereological analysis to study brain morphology in patients with medically intractable temporal lobe epilepsy; and to determine the relation between side, duration, and age of onset of temporal lobe epilepsy, history of childhood febrile convulsions, and grey matter structure. Methods: Three dimensional magnetic resonance images were obtained from 58 patients with left sided seizure onset (LSSO) and 58 patients with right sided seizure onset (RSSO), defined using EEG and foramen ovale recordings in the course of presurgical evaluation for temporal lobectomy. Fifty eight normal controls formed a comparison group. VBM was used to characterise whole brain grey matter concentration, while the Cavalieri method of modern design stereology in conjunction with point counting was used to estimate hippocampal and amygdala volume. Age and sex were used as confounding covariates in analyses. Results: LSSO and RSSO patients showed significant reductions in volume (using stereology) and grey matter concentration (using VBM) of the hippocampus, but not of the amygdala, in the presumed epileptogenic zone when compared with controls, but hippocampal (and amygdala) volume and grey matter concentration were not related to duration or age of onset of epilepsy. LSSO and RSSO patients with a history of childhood febrile convulsions had reduced hippocampal volumes in the presumed epileptogenic zone compared with patients without such a history. Left amygdala volume was also reduced in LSSO patients with a history of childhood convulsions. VBM results indicated bilateral thalamic, prefrontal, and cerebellar GMC reduction in patients, which correlated with duration and age of onset of epilepsy. Conclusions: Hippocampal sclerosis is not necessarily the consequence of recurrent temporal lobe seizures. A major cause of hippocampal sclerosis appears to be an early aberrant neurological insult, such as childhood febrile seizures. Secondary brain abnormalities exist in regions outside the presumed epileptogenic zone and may result from recurrent seizures. H ippocampal sclerosis is the most common finding in patients with medically intractable temporal lobe epilepsy.1 However, the relation between the duration of epilepsy and hippocampal sclerosis is not fully understood. Some cross sectional research has found evidence for progressive hippocampal volume loss in patients with temporal lobe epilepsy, [2][3][4][5] suggesting that hippocampal atrophy is a consequence of recurrent temporal lobe seizures. Conversely, others have found no relation between hippocampal volume and duration of epilepsy, 6 7 which suggests that hippocampal abnormalities do not result from repeated seizures. Hippocampal sclerosis has been related to the age of onset of epilepsy and a history of childhood febrile convulsions in some studies.3 7 However, although atrophy of the amygdala, 8 9 entorhinal cortex, 10-12 parahippocampal gyrus, 13 14 lateral temporal lobe, 15 16 and thalamus 17 h...

The aim of our study was to determine when foramen ovale recordings add useful information to scalp EEG recordings and magnetic resonance imaging (MRI) with hippocampal measurements. We evaluated the outcome of 79 patients with non-lesional partial epilepsy with presumed temporal seizure onset. Ictal foramen ovale recordings were performed in 16 patients with normal MRI (‘MRI-negative group’) and 41 patients with lateralizing MRI but non-lateralizing scalp EEG (‘discordant group’). 22 patients with concordant MRI and scalp EEG were not investigated with foramen ovale recordings (‘concordant group’). The seizure-free rate was higher in concordant than discordant patients despite additional investigation with foramen ovale electrodes (71 and 55% seizure free, respectively). No useful localizing information was added with foramen ovale recordings in MRI-negative patients.