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Pathological findings underlying focal temporal lobe hypometabolism in partial epilepsy
Author(s) -
Engel Jerome,
Brown W. Jaan,
Kuhl David E.,
Phelps Michael E.,
Mazziotta John C.,
Crandall Paul H.
Publication year - 1982
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410120604
Subject(s) - pathological , lesion , temporal lobe , ictal , medicine , epilepsy , pathology , lobe , radiology , psychiatry
Abstract Histopthogical studies were carried out on temporal lobe tissue from 25 patients with partial complex seizures who were studied by interictal positen computed tomography (PCT) with 18 F‐fluorodeoxyglucose and subsequently underwenty anterior lobe resection. Abnormalities were identified on x‐ray computed tomographic scane in 7 patients, but none indicated the site of a pathologically confirmed structural lesion. Hypometabolic zones were observed on PCT scans of 22 patients and corresponded to focal pathological abnormalities in 19 (15 mesial temporal sclerosis, 2 small neoplasms, 1 angioma, 1 heterotopia). In 1 patient with a foclly abnormal PCT scan and no pathological changes, the lesion may have been located posterior to the resection. In the remaining 2 patients, the hypometabolic zones later disappeared and may have represented a transient response reponse induced by depth electrode implantation. Three patients with normal PCT scans had no pathological abnormalities in their resected tissue. The degree of relative hypometabolism measured by PCT correlated well with the severity of the pathological lesion, byt the size of the hypometabolic zone was generally much larger than the area of pathological involvement. This discrepancy could not be considered an artifact of techique and muist represent either structural abnormalities below the resolution of routine histopathological studies (e.g., loss of synapses) or functional incativation of neuronal elements associated with the epileptogenic lesion.