VALUE OF MAGNETIC-RESONANCE-IMAGING - BASED MEASUREMENTS OF HIPPOCAMPAL FORMATIONS IN PATIENTS WITH PARTIAL EPILEPSY

Citation
C. Adam et al., VALUE OF MAGNETIC-RESONANCE-IMAGING - BASED MEASUREMENTS OF HIPPOCAMPAL FORMATIONS IN PATIENTS WITH PARTIAL EPILEPSY, Archives of neurology, 51(2), 1994, pp. 130-138
Citations number
53
Categorie Soggetti
Clinical Neurology
Journal title
ISSN journal
00039942
Volume
51
Issue
2
Year of publication
1994
Pages
130 - 138
Database
ISI
SICI code
0003-9942(1994)51:2<130:VOM-BM>2.0.ZU;2-Q
Abstract
Objective: To determine the occurrence of magnetic resonance imaging-d etected hippocampal atrophy (HA) in patients with partial epilepsy (te mporal and extratemporal, cryptogenic, or symptomatic). Magnetic reson ance imaging-detected HA has been demonstrated to be both sensitive an d specific for hippocampal sclerosis in cryptogenic temporal lobe epil epsy. Design: Patients' hippocampal formations were measured on a comp uterized system using Tl-weighted, 5-mm contiguous magnetic resonance coronal images made perpendicular to the hippocampus long axis. Hippoc ampal atrophy was defined on the basis of a normative asymmetry index and correlated with the epileptogenic focus defined by clinical, elect roencephalographic, and magnetic resonance imaging (apart from HA) loc alizing data. Patients and Control Subjects: Seventy patients with int ractable complex partial seizures of temporal, extratemporal,or undefi ned origin and 21 healthy control subjects. Results: Hippocampal atrop hy was present in 70% of patients with cryptogenic temporal lobe epile psy (TLE) (n=40), 44% of patients with symptomatic TLE (n=9), 29% of p atients with extratemporal epilepsy (n=14), and 6% of unclassified pat ients (n=16). In the cryptogenic TLE category, HA was marked and usual ly concordant (93%) with electroencephalographic lateralization. Hippo campal atrophy was often mild in the extratemporal epilepsy category. With the use of a wider confidence interval (+/- 3.1 SD instead of +/- 2.2 SD), HA specificity for TLE increased to 93%, HA specificity for lateralizing cryptogenic TLE reached 96%, and HA sensitivity for crypt ogenic TLE stood almost unchanged (68%). We found a link between early convulsions and HA occurrence. Conclusions: Hippocampal atrophy is a marker for TLE. Dual pathologic findings are detected in 44% of sympto matic TLE cases. Mild HA is rarely associated with extratemporal epile psy. Magnetic resonance imaging-based hippocampal volumetric analysis is a useful method to localize the origin of partial complex seizures.