Long-term seizure outcome in pediatric patients with focal cortical dysplasia undergoing tailored and standard surgical resections

Seizure. 2018 Nov:62:66-73. doi: 10.1016/j.seizure.2018.09.021. Epub 2018 Sep 26.

Abstract

Purpose: Focal cortical dysplasia (FCD) is the major cause of focal intractable epilepsy in childhood. Here we analyze the factors influencing the success of surgical treatment in a large cohort of children with histologically ascertained FCD.

Method: A retrospective study of the effects of FCD type, surgical intervention, and age at surgery in a pediatric cohort.

Results: A total of 113 patients (71 male; mean age at surgery 10.3 years; range 0-18) were analyzed; 45 had undergone lesionectomy, 42 lobectomy, 18 multi-lobectomy, and eight hemispherotomy. Complete seizure control (Engel Ia) was achieved in 56% after two years, 52% at five years, and 50% at last follow-up (18-204 months). Resections were more extensive in younger patients (40% of the surgeries affecting more than one lobe in patients aged nine years or younger vs. 22% in patients older than nine years). While resections were more limited in older children, their long-term outcome tended to be superior (42% seizure freedom in patients aged nine years or younger vs. 56% in patients older than nine years). The outcome in FCD I was not significantly inferior to that in FCD II.

Conclusions: Our data confirm the long-term efficacy of surgery in children with FCD and epilepsy. An earlier age at surgery within this cohort did not predict a better long-term outcome, but it involved less-tailored surgical approaches. The data suggest that in patients with an unclear extent of the dysplastic area, later resections may offer advantages in terms of the precision of surgical-resection planning.

Keywords: Children; Epilepsy surgery; Focal cortical dysplasia; Long-term outcome.

MeSH terms

  • Adolescent
  • Anticonvulsants / therapeutic use
  • Child
  • Child, Preschool
  • Cohort Studies
  • Electroencephalography
  • Epilepsy / complications
  • Epilepsy / diagnostic imaging
  • Epilepsy / surgery*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Magnetic Resonance Imaging
  • Male
  • Malformations of Cortical Development, Group I / complications
  • Malformations of Cortical Development, Group I / diagnostic imaging
  • Malformations of Cortical Development, Group I / surgery*
  • Neurosurgical Procedures / methods*
  • Recurrence
  • Treatment Outcome*

Substances

  • Anticonvulsants

Supplementary concepts

  • Focal cortical dysplasia of Taylor