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A Simple Cell-based Immunofluorescence Assay to Detect Autoantibody Against the N-Methyl-D-Aspartate (NMDA) Receptor in Blood
Published on: January 9, 2018
Anti-NMDA receptor encephalitis: a video case report
Angelo Labate1, Sarosh R Irani, Angela Vincent
1Institute of Neurology, University Magna Graecia, Catanzaro, Italy. a.labate@isn.cnr.it
Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis can present with unusual movement disorders. This case highlights lower limb stereotypical movements mimicking psychogenic seizures in anti-NMDAR encephalitis.
Area of Science:
- Neurology
- Immunology
- Oncology
Background:
- Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is an autoimmune disorder often associated with tumors.
- Paraneoplastic encephalitis frequently manifests with neuropsychiatric symptoms and hyperkinetic movements.
Observation:
- A 26-year-old Italian woman was diagnosed with anti-NMDAR encephalitis following incidental discovery of an ovarian tumor.
- The patient exhibited stereotypical movements primarily affecting the lower limbs, resembling psychogenic seizures.
Findings:
- The observed lower limb movements are atypical for anti-NMDAR encephalitis, which commonly presents with more generalized hyperkinetic or dyskinetic movements.
- This presentation expands the known clinical spectrum of movement disorders associated with anti-NMDAR encephalitis.
Implications:
- Recognizing atypical movement patterns is crucial for timely diagnosis of anti-NMDAR encephalitis.
- This case underscores the importance of considering autoimmune encephalitis in patients with unexplained neurological and psychiatric symptoms, even with unusual presentations.
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