Twenty-three infants and children underwent cortical resection (n = 15
) or hemispherectomy (n = 8) for intractable infantile spasms. Infanti
le spasms were present at the time of surgery in 17 of the 23 patients
; in six, spasms had evolved to other seizure types during surgical ev
aluation. Children with a remote history of infantile spasms were excl
uded from this study. Focal or hemispheric lesions were identified by
magnetic resonance imaging in seven children; an additional two showed
focal atrophy without a discrete lesion. Positron emission tomography
(PET) showed lateralized or localized abnormalities of cerebral gluco
se utilization in all patients; in 14, PET was the only neuroimaging m
odality to identify the epileptogenic cortex. When this occurred, neur
opathological examination of resected brain tissue typically showed ma
lformative and dysplastic cortical lesions. Focal interictal and/or ic
tal electrographic abnormalities were present in all patients, and cor
responded well with localization from neuroimaging. None of the patien
ts were subjected to chronic invasive electrographic monitoring with i
ntracranial electrodes. At follow-up (range 4-67 months; mean 28.3 mon
ths), 15 children were seizure-free, three had 90% seizure control, on
e had 75% seizure control, and four failed to benefit from surgery wit
h respect to seizure frequency.