Cerebral (18)FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-D-aspartate receptor encephalitis: A case series

authors

• Lagarde Stanislas
• Lepine Anne
• Caietta Emilie
• Pelletier Florence
• Boucraut José
• Chabrol Brigitte
• Milh Mathieu
• Guedj Eric

keywords

• Adolescent
• Anti-NMDAR
• Anti-N-Methyl-D-Aspartate Receptor Encephalitis
• Autoantibodies
• Autoimmune
• Brain FDG-PET
• Cerebral FDG-PET
• Child
• Preschool
• Children
• Electroencephalography
• Encephalitis
• Female
• Fluorodeoxyglucose F18
• FluoroDeoxy-Glucose Positron Emission Tomography
• Glucose
• Humans
• Magnetic Resonance Imaging
• Male
• N-methyl-d-aspartate
• Positron-Emission Tomography
• Radiopharmaceuticals
• Retrospective Studies
• Rituximab

abstract

BACKGROUND: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a frequent and severe cause of encephalitis in children with potential efficient treatment (immunotherapy). Suggestive clinical features are behavioural troubles, seizures and movement disorders. Prompt diagnosis and treatment initiation are needed to guarantee favourable outcome. Nevertheless, diagnosis may be challenging because of the classical ancillary test (magnetic resonance imaging (MRI), electroencephalogram, standard cerebro-spinal fluid analysis) have limited sensitivity. Currently, immunological analyses are needed for the diagnostic confirmation. In adult patients, some studies suggested a potential role of cerebral (18)FluoroDeoxy-Glucose Positron Emission Tomography (FDG-PET) in the evaluation of anti-NMDAR encephalitis. Nevertheless, almost no data exist in paediatric population.ăMETHOD: We report retrospectively clinical, ancillary tests and cerebral FDG-PET data in 6 young patients (median age=10.5 years, 4 girls) with immunologically confirmed anti-NMDAR encephalitis.ăRESULTS: Our patients presented classical clinical features of anti-NMDAR encephalitis with severe course (notably four patients had normal MRI). Our series shows the feasibility and the good sensitivity of cerebral FDG-PET (6/6 patients with brain metabolism alteration) in paediatric population. We report some particular features in this population: extensive, symmetric cortical hypometabolism especially in posterior areas; asymmetric anterior focus of hypermetabolism; and basal ganglia hypermetabolism. We found also a good correlation between the clinical severity and the cerebral metabolism changes. Moreover, serial cerebral FDG-PET showed parallel brain metabolism and clinical improvement.ăCONCLUSION: Our study reveals the existence of specific patterns of brain metabolism alteration in anti-NMDAR encephalitis in paediatric population.

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