Anti‐LGI1 encephalitis preceded by psychiatric symptoms: A case report

Abstract

Abstract Background To date, only a few reports of anti‐LGI1 encephalitis with isolated psychiatric symptoms in the initial phase have been reported. We present a relatively rare case of antileucine‐rich glioma‐inactivated 1 (LGI1) encephalitis that developed only psychiatric symptoms at the onset. Case Presentation The patient was a male in his 40s who developed anxiety and panic symptoms and was started on antidepressants after being diagnosed with panic disorder by a psychiatrist. He visited our hospital 2 months later presenting with hallucinations, delusions, mild cognitive decline, and faciobrachial dystonic seizures in the left upper extremity and face. Fluid‐attenuated inversion recovery magnetic resonance imaging revealed swelling and hyperintensities in the right caudate nucleus and putamen. Cerebrospinal fluid analysis did not show increased protein levels or cell counts and revealed positive oligoclonal bands. Subsequently, positive results for anti‐LGI1 antibodies were observed in the cerebrospinal fluid. Therefore, the patient was diagnosed with anti‐LGI1 encephalitis. Conclusion This case highlights the need to consider anti‐LGI1 encephalitis therapy in patients with acute‐onset psychiatric symptoms.

Keywords

• antileucine‐rich glioma‐inactivated 1 encephalitis
• anti‐N‐methyl‐D‐aspartate receptor encephalitis
• autoimmune encephalitis
• psychosis
• seizures