Archives of Epilepsy (Aug 2018)

Band Heterotopia and Lennox-Gastaut Syndrome: A Case Report

  • Mehmet Fatih GÖL,
  • Füsun Ferda ERDOĞAN

DOI
https://doi.org/10.14744/epilepsi.2018.36349
Journal volume & issue
Vol. 24, no. 2
pp. 83 – 86

Abstract

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Heterotopia, referred to as a limited or common neuronal migration disorder, may manifest clinically with mild mental retardation, epileptic seizures, psychiatric symptoms, or systemic disorders. Approximately 90% of cases have drug-resistant epileptic seizures. Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy with cognitive impairment; it is treatment-resistant and has a poor prognosis, with multiple patterns of seizures and specific electroencephalographic (EEG) patterns. In this case, the brain imaging showed band heterotopy, an EEG 2–2.5 Hz spike wave, and multiple spike and fast rhythms. This case of a 17-year-old male patient with drug-resistant tonic, atonic, myoclonic, atypical absence seizures, and behavioral abnormalities who was diagnosed with LGS was presented to highlight the difficulty in treatment management.

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