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Can Ictal F18-FDG PET/CT Drawing Epileptogenic Zone in Refractory Focal Epilepsy? Histopathological and Outcome Correlation | OMICS International | Abstract
ISSN: 2472-0895

Epilepsy Journal
Open Access

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Research Article

Can Ictal F18-FDG PET/CT Drawing Epileptogenic Zone in Refractory Focal Epilepsy? Histopathological and Outcome Correlation

David Ladrón de Guevara1-3*, Manuel Campos3,4, Francesca Solari3, Loreto Ríos3, Gisela Kuester2,3, Marcelo Gálvez1,3 and Felipe Otayza3,4

1Department of Radiology, Clínica Las Condes, Santiago, Chile

2Universidad de Chile, Santiago, Chile

3Advanced Epilepsy Center, Clínica Las Condes, Santiago, Chile

4Department of Neurosurgery, Clínica Las Condes, Santiago, Chile

*Corresponding Author:
David Ladrón de Guevara
Advanced Epilepsy Center
Universidad de Chile
Clínica Las Condes Santiago, Chile
Tel: 56 2 22105174
E-mail: [email protected]

Received date: June 06, 2016; Accepted date: July 04, 2016; Published date: July 10, 2016

Citation: de Guevara DL, Campos M, Solari F, Ríos L, Kuester G, et al. (2016) Can Ictal F18-FDG PET/CT Drawing Epileptogenic Zone in Refractory Focal Epilepsy? Histopathological and Outcome Correlation. J Epilepsy 2:109. doi:10.4172/2472-0895.1000109

Copyright: © 2016 de Guevara DL, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Unlike interictal Positron Emission Tomography (PET), ictal PET is not regularly used in the study of refractory focal epilepsy, and its usefulness in presurgical evaluations, and prognosis value have not been established. The aim is to present six patients with epilepsy whose PET/CT brain scans showed focal hypermetabolism, and analyze their correlation with the histopathological findings and clinical results. We reviewed 146 18F-FDG PET/CT scans performed on patients with refractory focal epilepsy. Only those cases with hypermetabolic foci which were subsequently surgically resected were selected. The epidemiological and clinical data were reviewed in addition to the brain MRI, Electroencephalography (EEG), video-EEG monitoring, intraoperative Electrocorticography (ECoG), histopathology, and postsurgical outcome. The PET findings were correlated with the clinical characteristics of the seizures, the EEG, brain MRI, ECoG, and histopathology. Seven PET/CT scans carried out on six patients showed well-defined hypermetabolic foci (three temporal, four extratemporal). There was a high correlation between the clinical lateralization, EEG/ECoG findings, and hypermetabolic foci located by PET. An MRI correctly identified the resected histopathological lesion in five cases and it was negative in two. Three patients had Focal Cortical Dysplasia (FCD), one had FCD with areas of polymicrogyria, one had temporal lobe cavernoma associated with hippocampal sclerosis, and one had a focal subcortical heterotopia. Mean postsurgical follow-up was 29.1 months (range: 16-24 months) and all patients were seizure free during this period. This small series of patients who underwent surgery for intractable focal epilepsy have shown good correlation between the ictal F18-FDG PET/CT scan and the electroclinical and pathological findings. These results suggest that hypermetabolic foci showed in PET/CT provides a reliable estimation of epileptogenic zone. Focus size underestimation in one case suggest the need of doing an interictal PET before surgery.

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