To determine seizure propagation patterns, we analyzed ictal positron
emission tomography (PET) studies of regional cerebral glucose utiliza
tion in 18 children (11 male and 7 female aged 2 weeks to 16 years) wi
th epilepsy (excluding infantile spasms IS). Three major metabolic pat
terns were determined based on degree and type of subcortical involvem
ent: Nine children had type I; asymmetric glucose metabolism of striat
um and thalamus. Of these, the 7 oldest children showed unilateral cor
tical hypermetabolism (always including frontal cortex) and crossed ce
rebellar hypermetabolism. Two infants (aged <1 year) had a similar ict
al PET pattern but no cerebellar asymmetry, presumably owing to immatu
rity of corticopontocerebellar projections. Five children had type II,
symmetric metabolic abnormalities of striatum and thalamus; this patt
ern was accompanied by hippocampal or insular cortex hypermetabolism,
diffuse neocortical hypometabolism and absence of any cerebellar abnor
mality. Four children had type III, hypermetabolism restricted to cere
bral cortex. This classification can accommodate ictal PET and single
photon emission computed tomography (SPECT) patterns described by othe
r investigators. Future studies should be directed at the clinical rel
evance of this classification, particularly with regard to epilepsy su
rgery.