Autoimmune Encephalitis With Positive Anti-Leucine-Rich Glioma-Inactivated 1 (Anti-LGI1) Antibody Mimicking Psychogenic Non-epileptic Seizures

Autoimmune encephalitis (AIE) represents a significant cause of neurological and psychiatric disorders, often initially misdiagnosed due to a diverse clinical presentation. This case describes a middle-aged woman initially diagnosed with psychogenic non-epileptic seizures (PNES) following emotional stress and depressive symptoms after a family bereavement. Progressive involuntary jerky movements, cognitive dysfunction, and a generalized tonic-clonic seizure raised suspicion for AIE. Diagnostic imaging showed medial temporal lobe hyperintensities, and serological testing confirmed high titers of anti-leucine-rich glioma-inactivated 1 (LGI1) antibodies. The patient showed significant improvement after receiving pulse steroid therapy and intravenous immunoglobulin (IVIG). This case highlights the importance of recognizing psychiatric and neurological overlap in anti-LGI1 encephalitis, emphasizing the need for prompt diagnostic evaluation and early immunomodulatory treatment to optimize patient outcomes.

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Journal
Cureus
Published
2025-10-08
DOI
https://doi.org/10.7759/cureus.94129
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
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article

Autoimmune Encephalitis With Positive Anti-Leucine-Rich Glioma-Inactivated 1 (Anti-LGI1) Antibody Mimicking Psychogenic Non-epileptic Seizures

Pushparaja Shetty, Sidra Akram, Ahmer A Longi, Misbah Fazlani et al.
Cureus
Autoimmune Neurological Disorders and Treatments
article

Autoimmune Encephalitis With Positive Anti-Leucine-Rich Glioma-Inactivated 1 (Anti-LGI1) Antibody Mimicking Psychogenic Non-epileptic Seizures

Pushparaja Shetty, Sidra Akram, Ahmer A Longi, Misbah Fazlani, Kasid Nouri
article en

Abstract

Autoimmune encephalitis (AIE) represents a significant cause of neurological and psychiatric disorders, often initially misdiagnosed due to a diverse clinical presentation. This case describes a middle-aged woman initially diagnosed with psychogenic non-epileptic seizures (PNES) following emotional stress and depressive symptoms after a family bereavement. Progressive involuntary jerky movements, cognitive dysfunction, and a generalized tonic-clonic seizure raised suspicion for AIE. Diagnostic imaging showed medial temporal lobe hyperintensities, and serological testing confirmed high titers of anti-leucine-rich glioma-inactivated 1 (LGI1) antibodies. The patient showed significant improvement after receiving pulse steroid therapy and intravenous immunoglobulin (IVIG). This case highlights the importance of recognizing psychiatric and neurological overlap in anti-LGI1 encephalitis, emphasizing the need for prompt diagnostic evaluation and early immunomodulatory treatment to optimize patient outcomes.

CureusVol. 17(10)
Mediclinic City Hospital (AE)
Openalex Percentile: Top 60%
Autoimmune Neurological Disorders and Treatments
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Autoimmune Encephalitis With Positive Anti-Leucine-Rich Glioma-Inactivated 1 (Anti-LGI1) Antibody Mimicking Psychogenic Non-epileptic Seizures — Pushparaja Shetty, Sidra Akram, et al. · Cureus (2025) | TGRS Research Map | TGRS