Korean J Pathol.
1999 Dec;33(12):1175-1181.
Comparison of Pathologic Findings of Cortical Lobectomy for Intractable Seizures between Children and Adults: An Analysis of 164 Cases
- Affiliations
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- 1Department of Diagnostic Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
Abstract
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Many pathological surveys of brain tissue in patients with intractable epilepsy have been
reported. There have been, however, few studies focused on the differences between
childhood and adults in pathological alterations of brain. We retrospectively analyzed
histopathology of 164 lobectomy specimens for intractable epilepsy in view of the
differences between children and adults. Among 164 cases, 28 cases were children (less
than 15 years) and 136 cases adults. We compared frequency of histopathologic features,
distribution of involved cortex (temporal or extratemporal lobe), previous injury histories,
such as brain trauma, encephalitis or febrile seizure, and coexistence of other lesions
(dual pathology) between two groups. Pathologic alterations were encountered in 92% of
164 patients. In children focal cortical dysplasia (n=16, 57.1%), neoplasm (n=8, 28.6%),
hippocampal sclerosis (n=6, 21.4%), cortical tuber (n=1, 3.6%), leukomalacia (n=1, 3.6%),
and Rasmussen's encephalitis (n=1, 3.6%) were observed, whereas focal cortical
dysplasia (n=81, 59.6%), hippocampal sclerosis (n=80, 58.8%), neoplasm (n=19, 14%), and
cerebral cysticercosis (n=3, 2.2%) were found in adults. Pediatric patients had a higher
proportion of severe focal cortical dysplasia (17.9% in children, 0.7% in adults). Neoplasia
and extratemporal lobe involvement were more commonly found in children (28.6%, 50%)
than in adults (14.0%, 24.3%), whereas hippocampal sclerosis and dual pathology were
more common in adults (58.8%, 44.9%) than in children (21.4%, 17.9%). Previous injury
history was statistically significant in patients with hippocampal sclerosis, and lent
support to the hypothesis that hippocampal sclerosis is related with acquired lesions.
Incidence of focal cortical dysplasia was nearly similar in both adult (59.6%) and
pediatric groups (57.1%), and supported the hypothesis that focal cortical dysplasia is
developmental abnormality occurring during a prenatal period.