We performed a retrospective database analysis as part of an internal audit to identify patients evaluated between 2003 and 2018 with definite diagnosis of AE according to Graus and colleagues’ Position Paper [3 (link)]. We identified 6 patients in whom potential differential diagnoses were excluded by adequate tests, and who underwent autoantibodies analysis, MRI and electroencephalogram (EEG). Additionally, an early brain FDG-PET study was performed in all cases within the first week from the onset of symptoms. A whole-body –FDG-PET scan was added to the paraneoplastic workup of AE screening for malignancy in three patients (cases 1, 2 and 5). Patients fasted for at least 4 h before the study. Forty minutes after the injection of 336.7 ± 72.7 MBq of 18Fluorine-fluorodeoxyglucose, a 20-min PET/CT scan was acquired. All patients were scanned in a Siemens Biograph mCT TrueV. Acquisition and reconstruction were performed with the standard protocol for brain studies, as previously described [20 (link)]. Informed consent was obtained from all individual participants included in the study. Additional informed consent was obtained from all individual participants from whom identifiable information is included in this article.
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