Adult occipital lobe epilepsy: 12-years on

J Neurol. 2021 Oct;268(10):3926-3934. doi: 10.1007/s00415-021-10557-y. Epub 2021 Apr 26.

Abstract

Objective: Occipital lobe epilepsies (OLE) comprise 5-10% of focal epilepsies in surgical and paediatric series; with little data from adult medical cohorts. This longitudinal study examined OLE patients, to characterise prevalence, semiology, co-morbidity and prognosis in a neurology outpatient setting.

Methods: 24 adult OLE patients identified over 12 months from 1548 patients in a neurologist's service were followed over 12 years.

Results: 92% of these OLE patients had simple visual hallucinations, misdiagnosed in 40% of cases. 75% had co-morbid interictal migraine and 38% had visual field defects. Only 33% achieved long-term remission, and only 2 /10 (20%) of OLE patients with a structural aetiology were seizure-free. The two patients with migralepsy achieved remission.

Conclusion: Adult OLE accounted for 7.7% of focal epilepsies in this cohort, misdiagnosed or misclassified in 40%. Most patients had co-existing migraine. A minority had migralepsy characterised by a longer aura and good prognosis. Remission rates were lower than that of childhood OLE and general adult epilepsy populations, strengthening the argument for considering epilepsy surgery in drug-resistant OLE patients with a structural cause. Precision medicine will potentially refine diagnosis and management in those OLE patients without an identified cause but is predicated on accurate clinical phenotyping.

Keywords: Focal epilepsy; Migraine; Migralepsy; Occipital epilepsy; Occipital seizures; Visual aura; Visual hallucinations.

MeSH terms

  • Adult
  • Child
  • Drug Resistant Epilepsy*
  • Electroencephalography
  • Epilepsies, Partial* / diagnosis
  • Epilepsies, Partial* / epidemiology
  • Epilepsy*
  • Humans
  • Longitudinal Studies
  • Occipital Lobe