Frontiers in Neurology (Dec 2021)

Case Report: Hemispherotomy in the First Days of Life to Treat Drug-Resistant Lesional Epilepsy

  • Konstantin L. Makridis,
  • Konstantin L. Makridis,
  • Konstantin L. Makridis,
  • Christine Prager,
  • Christine Prager,
  • Anna Tietze,
  • Deniz A. Atalay,
  • Deniz A. Atalay,
  • Sebastian Triller,
  • Sebastian Triller,
  • Christian E. Elger,
  • Christian E. Elger,
  • Christian E. Elger,
  • Ulrich-Wilhelm Thomale,
  • Angela M. Kaindl,
  • Angela M. Kaindl,
  • Angela M. Kaindl

DOI
https://doi.org/10.3389/fneur.2021.818972
Journal volume & issue
Vol. 12

Abstract

Read online

Background: Neonatal drug-resistant epilepsy is often caused by perinatal epileptogenic insults such as stroke, ischemia, hemorrhage, and/or genetic defects. Rapid seizure control is particularly important for cognitive development. Since early surgical intervention and thus a short duration of epilepsy should lead to an optimal developmental outcome, we present our experience with hemispherotomy in an infant at the corrected age of 1 week.Methods: We report successful hemispherotomy for drug-resistant epilepsy in an infant with hemimegalencephaly at a corrected age of 1 week.Results: The infant was diagnosed with drug-resistant lesional epilepsy due to hemimegalencephaly affecting the left hemisphere. Given congruent electroclinical findings, we performed a left vertical parasagittal transventricular hemispherotomy after critical interdisciplinary discussion. No complications occurred during the surgery. Intraoperatively; 118 ml of red blood cells (30 ml/kg) and 80 ml of plasma were transfused. The patient has been seizure-free since discharge without further neurological deficits.Conclusion: We demonstrate that early epilepsy surgery is a safe procedure in very young infants if performed in a specialized center experienced with age-specific surgical conditions and perioperative management. The specific surgical difficulties should be weighed against the risk of life-long developmental drawbacks of ongoing detrimental epilepsy.

Keywords