顽固性局灶性癫痫发作时F18-FDG PET/CT能画出致痫区吗?组织病理学和预后相关性

D. Dl, M. Campos, F. Solari, L. Ríos, G. Kuester, M. Gálvez, F. Otayza
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引用次数: 1

摘要

与间歇期正电子发射断层扫描(PET)不同,间歇期PET不常用于难治性局灶性癫痫的研究,其在术前评估和预后价值方面的作用尚未确定。目的是介绍6例癫痫患者的PET/CT脑扫描显示局灶性高代谢,并分析其与组织病理学和临床结果的相关性。我们回顾了146例难治性局灶性癫痫患者的18F-FDG PET/CT扫描。只选择那些随后手术切除的高代谢灶病例。我们回顾了流行病学和临床资料,以及脑MRI、脑电图(EEG)、视频脑电图监测、术中皮质电图(ECoG)、组织病理学和术后结果。PET的发现与癫痫发作的临床特征、脑电图、脑MRI、ECoG和组织病理学相关。对6例患者进行的7次PET/CT扫描显示明确的高代谢灶(3例颞部,4例颞外)。临床侧化、EEG/ECoG结果与PET定位的高代谢灶之间存在高度相关性。MRI正确识别了5例切除的组织病理病变,2例为阴性。3例患者有局灶性皮质发育不良(FCD), 1例FCD伴多小回区,1例颞叶海绵状瘤伴海马硬化,1例局灶性皮质下异位。术后平均随访29.1个月(16 ~ 24个月),随访期间无癫痫发作。这一小组接受顽固性局灶性癫痫手术的患者显示,F18-FDG PET/CT扫描与电临床和病理表现具有良好的相关性。这些结果表明,PET/CT显示的高代谢灶提供了可靠的癫痫区估计。一个病例的病灶大小低估提示术前需要进行间歇PET检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Ictal F18-FDG PET/CT Drawing Epileptogenic Zone in Refractory Focal Epilepsy? Histopathological and Outcome Correlation
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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