18 F-FDG PET Brain Findings in a Case of Idiopathic Benign Rolandic Epilepsy of Childhood

Kousik Vankadari1, Rajender Kumar2, Bhagwant Rai Mittal2

  • 1Department of Nuclear Medicine, Yashoda Hospital, Secunderabad, Telangana, India.

Insights

Idiopathic benign rolandic epilepsy, or benign childhood epilepsy with centrotemporal spikes (BCECTS), is common in children. This case highlights a rare instance of BCECTS refractory to medication, with brain imaging revealing specific metabolic changes.

Area of Science:

  • Pediatric Neurology
  • Epileptology
  • Neuroimaging

Background:

  • Idiopathic benign rolandic epilepsy, also known as benign childhood epilepsy with centrotemporal spikes (BCECTS), is a common epilepsy syndrome in children.
  • It typically has a favorable prognosis and is characterized by specific EEG findings.

Observation:

  • A 5-year-old female presented with focal seizures involving the right side of her face since 6 months of age.
  • She had normal development, unremarkable neurological examination, and no perinatal insults.
  • Electroencephalogram confirmed rolandic spikes suggestive of BCECTS.

Findings:

  • The patient's seizures were refractory to two antiepileptic drugs.
  • Brain MRI showed no structural lesions.
  • Interictal 18F-FDG PET revealed hypometabolism in the left lower rolandic region.

Implications:

  • This case illustrates a rare presentation of refractory BCECTS.
  • Neuroimaging, particularly 18F-FDG PET, may reveal metabolic changes even in the absence of structural lesions in some epilepsy syndromes.
  • Further research into the neurobiological underpinnings of refractory BCECTS is warranted.