Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26927
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dc.contributor.authorBerlangieri, Salvatore U-
dc.contributor.authorMito, R-
dc.contributor.authorSemmelroch, M-
dc.contributor.authorPedersen, M-
dc.contributor.authorJackson, G-
dc.date2020-12-15-
dc.date.accessioned2021-07-05T06:10:22Z-
dc.date.available2021-07-05T06:10:22Z-
dc.date.issued2020-12-15-
dc.identifier.citationEuropean Journal of Hybrid Imaging 2020; 4(1): 23en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26927-
dc.description.abstractBottom-of-sulcus dysplasia (BOSD) is a type of focal cortical dysplasia and an important cause of intractable epilepsy. While the MRI features of BOSD have been well documented, the contribution of PET to the identification of these small lesions has not been widely explored. The aim of this study was to investigate the role of F-18 fluorodeoxyglucose (18F-FDG) PET in the identification of BOSD. Twenty patients with BOSD underwent both 18F-FDG PET and structural MRI scans as part of preoperative planning for surgery. Visual PET analysis was performed, and patients were classified as positive if they exhibited a focal or regional hypometabolic abnormality, or negative in the absence of a hypometabolic abnormality. MRI data were reviewed to determine if any structural abnormality characteristic of BOSD were observed before and after co-registration with PET findings. PET detected hypometabolic abnormalities consistent with the seizure focus location in 95% (19/20) of cases. Focal abnormalities were detected on 18F-FDG PET in 12/20 (60%) patients, while regional hypometabolism was evident in 7/20 (35%). BOSD lesions were missed in 20% (4/20) of cases upon initial review of MRI scans. Co-registration of 18F-FDG PET with MRI enabled detection of the BOSD in all four cases where the lesion was initially missed. Our findings show that 18F-FDG PET provides additional clinical value in the localisation and detection of BOSD lesions, when used in conjunction with MRI.en
dc.language.isoeng
dc.subject18F-FDG PETen
dc.subjectBottom-of-sulcus dysplasiaen
dc.subjectFocal cortical dysplasiaen
dc.subjectMRIen
dc.titleBottom-of-sulcus dysplasia: the role of 18F-FDG PET in identifying a focal surgically remedial epileptic lesion.en
dc.typeJournal Articleen
dc.identifier.journaltitleEuropean Journal of Hybrid Imagingen
dc.identifier.affiliationDepartment of Psychology and Neuroscience, Auckland University of Technology, Auckland, New Zealanden
dc.identifier.affiliationFlorey Department of Neuroscience and Mental Health, The University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australiaen
dc.identifier.doi10.1186/s41824-020-00092-wen
dc.type.contentTexten
dc.identifier.orcid0000-0003-3945-2293en
dc.identifier.pubmedid34191213
local.name.researcherBerlangieri, Salvatore U
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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