Diffusion-weighted and perfusion MRI demonstrates parenchymal changes in complex partial status epilepticus

Kristina Szabo1, Annkathrin Poepel, Bernd Pohlmann-Eden

  • 1Department of Neurology, Universitätsklinikum Mannheim, University of Heidelberg, Mannheim, Germany.

Insights

Diffusion-weighted MRI (DWI) and perfusion imaging (PI) reveal brain changes during complex partial status epilepticus (CPSE). These advanced MRI techniques visualize temporary tissue and blood flow alterations in epilepsy patients.

Area of Science:

  • Neuroimaging
  • Epileptology
  • Radiology

Background:

  • Diffusion-weighted MRI (DWI) and perfusion imaging (PI) are primarily used for acute stroke but show potential in epilepsy's peri-ictal phase.
  • Previous studies suggest transient reductions in apparent diffusion coefficient (ADC) and hyperperfusion occur in experimental and human epilepsy.

Purpose of the Study:

  • To investigate the utility of serial DWI and PI in patients experiencing complex partial status epilepticus (CPSE).
  • To correlate MRI findings with clinical course, EEG, and SPECT data.

Main Methods:

  • Serial MRI, including DWI and PI, was performed on 10 patients with CPSE.
  • Apparent diffusion coefficient (ADC) values and perfusion changes were analyzed in specific brain regions.
  • SPECT studies were used for confirmation in select cases.

Main Results:

  • All patients exhibited regional hyperintensity on DWI with reduced ADC in the hippocampus, thalamus (pulvinar), and/or cortex.
  • A strong spatial correlation was observed between focal hyperperfusion and areas of ADC/DWI abnormality.
  • Follow-up MRIs demonstrated resolution of diffusion and perfusion abnormalities.

Conclusions:

  • Combined PI and DWI effectively visualize hemodynamic and tissue changes in the hippocampus, thalamus, and cortex following CPSE.
  • MRI findings correlate with prolonged epileptic activity, as supported by clinical, EEG, and SPECT data.
  • DWI and PI offer valuable insights into the peri-ictal phase of epilepsy.