Dysplastic Cerebellar Epilepsy: Complete Seizure Control Following Resection of a Ganglioglioma

Cerebellum. 2016 Aug;15(4):535-41. doi: 10.1007/s12311-015-0705-5.

Abstract

Subcortical epilepsy has been a controversial issue, partially settled by evidence showing seizure generation in hypothalamic hamartomas and also by reports of seizures caused by cerebellar lesions. We report 4-year-old girl with right hemifacial seizures and autonomic phenomena, in whom MRI showed an irregular mass in the right cerebellar peduncle. Despite several unremarkable video-EEG recordings, seizure origin in the lesion was hypothesized. Complete resection was feasible, histopathology showed a ganglioglioma, and she has been seizure free for 3 years. A fine line separates these developmental tumors from focal cortical dysplasia, and the homogeneous presentation of this entity led us to propose the terminology dysplastic cerebellar epilepsy.

Keywords: Cerebellar epilepsy; Epilepsy surgery; Ganglioglioma; Hemifacial spasms; Posterior fossa tumor.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Cerebellar Neoplasms / complications
  • Cerebellar Neoplasms / diagnostic imaging
  • Cerebellar Neoplasms / physiopathology
  • Cerebellar Neoplasms / surgery*
  • Cerebellum / diagnostic imaging
  • Cerebellum / pathology
  • Cerebellum / physiopathology
  • Cerebellum / surgery*
  • Child, Preschool
  • Epilepsy / diagnostic imaging
  • Epilepsy / etiology
  • Epilepsy / physiopathology
  • Epilepsy / surgery*
  • Female
  • Ganglioglioma / complications
  • Ganglioglioma / diagnostic imaging
  • Ganglioglioma / physiopathology
  • Ganglioglioma / surgery*
  • Humans
  • Seizures / diagnostic imaging
  • Seizures / etiology
  • Seizures / physiopathology
  • Seizures / surgery*
  • Treatment Outcome