Temporal lobe developmental malformations and hippocampal sclerosis: epilepsy surgical outcome

R Kuzniecky1, S S Ho, R Martin

  • 1University of Alabama at Birmingham Epilepsy Center, Department of Neurology, University of Alabama at Birmingham, 35294-0021, USA.

Neurology
|February 20, 1999
PubMed
Abstract

Insights

Temporal lobe developmental malformations often show bilateral hippocampal or amygdala atrophy. This atrophy, particularly in the amygdala, is linked to worse seizure outcomes after surgery for epilepsy.

Area of Science:

  • Neurology
  • Neurosurgery
  • Radiology

Background:

  • Temporal lobe developmental malformations frequently co-occur with mesial temporal sclerosis.
  • Dual pathology involving bilateral amygdala or hippocampal abnormalities is common.

Purpose of the Study:

  • To correlate and compare MRI findings and surgical outcomes.
  • To evaluate patients with temporal lobe developmental malformations versus isolated mesial temporal sclerosis.

Main Methods:

  • MRI-based normalized volumetry of amygdala and hippocampal formation.
  • Comparison of seizure outcomes post-temporal lobe resection.

Main Results:

  • Higher frequency of bilateral hippocampal/amygdala atrophy in developmental malformations.
  • No significant difference in seizure-free status between groups.
  • Worse surgical outcome in developmental malformations with bilateral amygdala/hippocampal-amygdala atrophy.

Conclusions:

  • Bilateral hippocampal atrophy is common in temporal lobe developmental malformations.
  • Bilateral amygdala or amygdalo-hippocampal atrophy predicts a higher risk of seizure recurrence.