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.
Abstract:
Idiopathic benign rolandic epilepsy, also known as benign childhood epilepsy with centrotemporal spikes (BCECTS), is one of the commonly seen electroclinical epilepsy syndromes of childhood with a generally favorable long-term prognosis. We describe a 5-year-old female child who presented with recurrent focal seizures involving right side of face since the age of 6 months. She had no perinatal or postnatal insults, had normal development, and her neurological examination was unremarkable. Electroencephalogram showed rolandic spikes, suggesting BCETCS. Her seizures remained refractory to two appropriately dosed antiepileptic drugs. Magnetic resonance imaging of the brain did not reveal any structural lesion. Interictal fluorodeoxyglucose 18 F-positron emission tomography brain showed hypometabolism in the left lower rolandic region.
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