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Temporal lobe epilepsy due to hippocampal sclerosis in pediatric candidates for epilepsy surgery

A Mohamed1, E Wyllie, P Ruggieri

  • 1Department of Neurology, The Cleveland Clinic Foundation, OH 44195, USA.

Neurology
|June 27, 2001
PubMed

Insights

Pediatric temporal lobe epilepsy (TLE) with hippocampal sclerosis (HS) shows similar features and seizure outcomes to adults. Dual pathology, common in children, does not negatively impact surgical results.

Area of Science:

  • Pediatric Neurology
  • Epileptology
  • Neuroimaging
  • Surgical Neurology

Background:

  • Temporal lobe epilepsy (TLE) with hippocampal sclerosis (HS) is a common cause of intractable seizures in children and adolescents.
  • Understanding the specific clinical, imaging, and histopathological features of pediatric TLE-HS is crucial for surgical planning and predicting outcomes.
  • Previous studies have primarily focused on adult populations, leaving a gap in knowledge regarding pediatric TLE-HS characteristics.

Purpose of the Study:

  • To comprehensively characterize the clinical, electroencephalography (EEG), magnetic resonance imaging (MRI), and histopathologic features of pediatric TLE caused by HS.
  • To explore the seizure outcomes following epilepsy surgery in this specific pediatric population.
  • To compare findings in children and adolescents with TLE-HS.

Main Methods:

  • Retrospective study of 17 children (4-12 years) and 17 adolescents (13-20 years) who underwent anteromesial temporal resection between 1990 and 1998.
  • Analysis included clinical seizure semiology, EEG findings (interictal spikes), MRI (hippocampal sclerosis, temporal neocortical abnormalities), and histopathology.
  • Seizure outcome was assessed at a mean follow-up of 2.6 years.

Main Results:

  • Seizures were characterized by decreased awareness and responsiveness, with varying automatisms between age groups.
  • MRI confirmed HS in all patients; subtle temporal neocortical abnormalities were frequent, especially in children.
  • Dual pathology (HS with cortical dysplasia) was found in 79% of patients, higher than expected, but did not predict poor surgical outcome.
  • Seventy-eight percent of patients achieved seizure freedom post-surgery, comparable to adult series.

Conclusions:

  • Pediatric TLE-HS presents with features similar to adults, occurring in children as young as 4 years.
  • Focal hippocampal atrophy may not always be evident in total hippocampal volumetry on MRI.
  • Children exhibit a high incidence of dual pathology, often predicted by MRI, but this does not adversely affect seizure control.
  • Epilepsy surgery for TLE-HS in pediatric patients yields outcomes comparable to those reported in adult studies.
Abstract

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