In carefully selected children, as well as adults, intractable seizure
s may be eliminated or greatly reduced by cortical resection or hemisp
herectomy. Critical features of surgical candidacy include intractable
disabling epilepsy, a localized epileptogenic zone, and a low risk of
new postoperative deficits; however, the analysis may be complicated
in children. Compared with adults, pediatric patients are especially l
ikely to present with poorly localizing electroencephalographic featur
es because of their high incidence of extratemporal localization and d
evelopmental pathology. Maturation factors may result in unusual epile
psy manifestations, for example, infantile spasms and hypsarrhythmia c
aused by a focal cortical lesion. The cognitive and psychosocial costs
of continued frequent seizures during infancy and childhood must be a
ssessed differently from those in adults and may include stagnation of
developmental progression. The risk for new postoperative deficits ma
y be modified if surgery is performed during stages of active brain ma
turation with developmental plasticity. For each individual child, the
potential risk/benefit ratio for surgery must be carefully weighed on
the basis of results of an extensive preoperative evaluation. Results
from pediatric epilepsy surgery series are encouraging, with percenta
ges of seizure-Tree patients similar to those in adult series. In some
series, delaying surgery for childhood-onset epilepsy into adulthood
was associated with greater permanent psychosocial, behavioral, and ed
ucational problems. The available data suggest that children should be
considered for surgical evaluation at whatever age they present with
severe intractable localization-related epilepsy. Complicated cases wa
rrant referral to specialized centers with extensive pediatric epileps
y surgery experience. (C) 1998 by Elsevier Science Inc. All rights res
erved.