Abstract
Autoimmune encephalitis (AIE) is a rare, severe, and rapidly progressive encephalopathy, and its diagnosis is challenging, especially in adolescent populations when the presentation is mainly psychiatric. Currently, cerebral 18-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) imaging is not included in the diagnosis algorithm. We describe a 16-year-old patient with probable seronegative encephalitis with catatonia for which several cerebral PET scans were relevant and helpful for diagnosis, treatment decision making, and follow-up monitoring. The patient recovered after 2 years of treatment with etiologic treatment of AIE and treatment of catatonia. This case suggests a more systematic assessment of the clinical relevance of 18F-FDG-PET imaging in probable seronegative AIE.
Original language | English |
---|---|
Article number | 685711 |
Journal | Frontiers in Psychiatry |
Volume | 12 |
DOIs | |
State | Published - 9 Jun 2021 |
Externally published | Yes |
Keywords
- abnormal movement
- adolescence
- catatonia
- cerebral PET/CT
- encephalitis