Neuroimaging and spectroscopy in children with epileptic encephalopathies
- Alasdair P J Parkera,
- Colin D Ferrieb,
- Steven Keevila,
- Marcus Newbolda,
- Timothy Coxa,
- Michael Maiseya,
- Richard O Robinsona
- aUnited Medical and Dental Schools, Guy’s Campus, London, UK, bDepartment of Paediatric Neurology, Leeds General Infirmary, Leeds, UK
- Dr A P J Parker, Newcomen Centre, Guy’s Hospital, London SE1 9RT, UK.
- Accepted 9 March 1998
Abstract
AIMS To investigate the nature of the unifocal cortical abnormalities on FDG positron emission tomography (PET) in children with an epileptic encephalopathy but no focal abnormality on electroencephalogram or standard magnetic resonance imaging (MRI).
METHODS Repeat FDG PET, surface rendered high resolution MRI, and single voxel magnetic resonance proton spectroscopy of the areas of abnormal metabolism compared to the contralateral side in 11 children aged 2 to 12 years. Imaging was repeated after a median of 13 months.
RESULTS Visual analysis of repeat FDG PET revealed similar abnormalities in 10 of 11 children. Semiquantitative analysis revealed similar sited abnormalities in eight children. One child with ictal hypermetabolism initially had an inconsistent second scan. Magnetic resonance spectra in three children showed the N-acetylaspartate/choline ratio was lower in the hypometabolic focus than in the reciprocal area on the opposite side, in two children it was higher, and in one child it was equal. Surface rendered MRI was normal in seven of eight children, and showed temporal lobe asymmetry in one.
CONCLUSION In children with established epileptic encephalopathies most hypometabolic areas on FDG PET are stable over time. While focal neuronal loss is likely in these areas in some children, microdysplasias or other focal cortical dysplasias are probable in others.
