{<sup>18</sup>F}fluorodeoxyglucose positron emission tomography in refractory complex partial seizures

William H. Theodore(National Institutes of Health), Michael Newmark(National Institutes of Health), Susumu Satô(National Institutes of Health), Rodney A. Brooks(National Institutes of Health), Nicholas J. Patronas(National Institutes of Health), Robert De La Paz(National Institutes of Health), Giovanni DiChiro(National Institutes of Health), Robert Kessler(National Institutes of Health Clinical Center), Richard Margolin(National Institutes of Health Clinical Center), Ronald G. Manning(National Institutes of Health Clinical Center), Michael A. Channing(National Institutes of Health Clinical Center), Roger J. Porter(National Institutes of Health)
Annals of Neurology
October 1, 1983
Cited by 251

Abstract

Positron emission tomography with simultaneous electroencephalographic monitoring was performed with [18F]fluorodeoxyglucose in 20 patients with complex partial seizures who had normal computed tomographic scans. Seven patients had only unilateral epileptiform discharges on the electroencephalogram, 3 had predominantly unilateral discharges, and 10 had nonlocalized epileptiform abnormalities. Positron emission tomography showed a hypometabolic lesion in 16 of the 20 patients. Pathological changes in the hypometabolic region were found in postoperative specimens in 4 of 5 patients studied. Positron emission tomography was unaffected by the seizure frequency, state of alertness, or number of spike discharges during the scan. There was a tendency for patients to have higher overall metabolic rates when taking less medication. Seizures occurring during [18F]fluorodeoxyglucose uptake in 3 patients produced a hypermetabolic area at the interictal hypometabolic focus. Positron emission tomography sometimes showed more widespread hypometabolism than suspected on the basis of the scalp-recorded electroencephalogram. The frontal lobe showed a greater degree of hypometabolism than the temporal lobe in 3 patients. Focal lesions may be identified by positron emission tomography even if the electroencephalographic abnormality is not well localized.


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