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dc.contributor.authorAydos, Uğuray
dc.contributor.authorArhan, Ebru
dc.contributor.authorAkdemir, Ümit Özgür
dc.contributor.authorAkbaş, Yılmaz
dc.contributor.authorAydın, Kürşad
dc.contributor.authorAtay, Lütfiye Özlem
dc.contributor.authorSerdaroğlu, Ayşe
dc.date.accessioned2020-09-11T10:48:42Z
dc.date.available2020-09-11T10:48:42Z
dc.date.issued2020en_US
dc.identifier.citationAydos, U., Arhan, E., Akdemir, Ü. Ö., Akbaş, Y., Aydın, K., Atay, L. Ö. ... Serdaroğlu, A. (2020). Utility of brain fluorodeoxyglucose PET in children with possible autoimmune encephalitis. Nuclear Medicine Communications, 41(8), 800-809. https://dx.doi.org/10.1097/MNM.0000000000001222en_US
dc.identifier.issn0143-3636
dc.identifier.issn1473-5628
dc.identifier.urihttps://dx.doi.org/10.1097/MNM.0000000000001222
dc.identifier.urihttps://hdl.handle.net/20.500.12511/5787
dc.description.abstractPurpose We aimed to explore the utility and additional clinical contribution of brain fluorodeoxyglucose (FDG) PET imaging for the assessment of children with possible autoimmune encephalitis in comparison to brain MRI. Materials and methods We conducted a retrospective analysis of six pediatric patients (all seronegative) between 2014 and 2019 with the initial diagnosis of possible autoimmune encephalitis who had brain FDG PET/CT or PET/MRI and brain MRI during the diagnostic period. Diagnosis of possible autoimmune encephalitis was based on clinical consensus criteria defined by Grauset al. Brain FDG PET images were visually evaluated. Semiquantitative evaluation was also performed by using the statistical parametric mapping (SPM) method. Results Cerebrospinal fluid pleiocytosis and electroencephalography abnormality were present in all patients. Mean duration between the onset of symptoms and brain FDG PET imaging was 33 +/- 16 days (range: 18-62 days). There were a total of eight brain FDG PET scans (six of PET/MRI and two of PET/CT). In two patients, FDG PET imaging was performed at diagnosis and follow-up. Initial FDG PET and SPM analysis findings were abnormal in all patients (100%), with four demonstrating only hypometabolism. Only a hypermetabolic pattern was seen in one patient, and mixed the hypohypermetabolic pattern was seen in one patient. All patients had metabolic abnormalities in temporal lobes. Additionally, visual and semiquantitative FDG PET findings revealed hypometabolism in extratemporal regions. Brain MRI was abnormal in two patients (33.3%) who had also FDG hypermetabolism in mesial temporal lobes. Conclusions Our findings support the usage of fluorine-18-FDG PET/computed tomography (CT)/MRI with quantitative analysis early in the diagnostic work-up of possible autoimmune encephalitis, particularly in those with normal or nonspecific MRI findings. However, it remains a purpose of further studies, if and to what extent FDG PET/CT or integrated FDG PET/MRI with quantitative analysis can improve the diagnostic workup of children with possible autoimmune encephalitis.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectAutoimmune Encephalitisen_US
dc.subjectBrain Fluorodeoxyglucose PETen_US
dc.subjectChildrenen_US
dc.subjectPETen_US
dc.subjectComputed Tomographyen_US
dc.subjectMRIen_US
dc.titleUtility of brain fluorodeoxyglucose PET in children with possible autoimmune encephalitisen_US
dc.typearticleen_US
dc.relation.ispartofNuclear Medicine Communicationsen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0003-1513-6149en_US
dc.identifier.volume41en_US
dc.identifier.issue8en_US
dc.identifier.startpage800en_US
dc.identifier.endpage809en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1097/MNM.0000000000001222en_US
dc.identifier.wosqualityQ4en_US
dc.identifier.scopusqualityQ3en_US


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