Abstract

Electroencephalography (EEG) has an important role in the diagnosis and classification of epilepsy. It can provide information for predicting the response to antiseizure drugs and to identify the surgically remediable epilepsies. In temporal lobe epilepsy (TLE) seizures could originate in the medial or lateral neocortical temporal region, and many of these patients are refractory to medical treatment. However, majority of patients have had excellent results after surgery and this often relies on the EEG and magnetic resonance imaging (MRI) data in presurgical evaluation. If the scalp EEG data is insufficient or discordant, invasive EEG recording with placement of intracranial electrodes could identify the seizure focus prior to surgery. This paper highlights the general information regarding the use of EEG in epilepsy, EEG patterns resembling epileptiform discharges, and the interictal, ictal and postictal findings in mesial temporal lobe epilepsy using scalp and intracranial recordings prior to surgery. The utility of the automated seizure detection and computerized mathematical models for increasing yield of non-invasive localization is discussed. This paper also describes the sensitivity, specificity, and predictive value of EEG for seizure recurrence after withdrawal of medications following seizure freedom with medical and surgical therapy.

Highlights

  • The previous ILAE classification of epilepsy syndromes classified temporal lobe epilepsy under medial temporal lobe and lateral temporal lobe epilepsy [1]

  • The MEDLINE literature search was performed for the EEG information and pertaining to all the aspects of the mesial temporal lobe epilepsy

  • The interictal changes in medial temporal lobe (mTLE) could be in the form of nonepileptiform abnormalities, epileptiform discharges, or both

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Summary

Introduction

The previous ILAE classification of epilepsy syndromes classified temporal lobe epilepsy under medial temporal lobe (mTLE) and lateral temporal lobe epilepsy (nTLE) [1]. MTLE is under “distinctive constellations/electroclinical syndromes” with the most common pathological substrate being hippocampal sclerosis (HS) [2, 3]. MTLE-HS is the most common form of focal epilepsy. It has a distinct clinical presentation called “limbic seizure” resulting from epileptic activity within the limbic structures; they are not distinguishable from mTLE with other pathologies than HS. MTLE-HS has specific electrographic features, neuroimaging, and pathological findings. The term hippocampal sclerosis denotes a specific pattern of cell loss mostly involving CA1 and hilar neurons and least the CA2 region [4]. Hippocampal sclerosis can be detected by high-resolution MRI in majority of patients [6, 7]

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