When the Mind Plays Tricks: LGI1 Encephalitis Mimicking Psychiatric Illness
Akshayaa K Aggarawal, Jithun v Varghese, Mansoor Gazi

TL;DR
This paper describes a case where a brain inflammation caused by the immune system mimicked a psychiatric illness and was eventually diagnosed and treated with steroids.
Contribution
The novelty lies in highlighting the diagnostic challenge of LGI1 encephalitis when initial tests are normal and the response to corticosteroid treatment.
Findings
LGI1 antibodies were detected in the patient's blood after initial normal MRI and EEG results.
Corticosteroid treatment led to cognitive improvement and fewer confusion episodes.
The patient's family reported reduced spasms following treatment.
Abstract
Autoimmune encephalitis (AE) is a rare brain inflammation caused by the immune system. Leucine-rich glioma inactivated 1 (LGI1) antibody-associated AE is more common in older men and presents with memory loss, confusion, and brief seizures called faciobrachial dystonic seizures (FBDS). We report a 66-year-old man with hypertension and high cholesterol who presented with sleep-related spasms, confusion, and cognitive decline. Early magnetic resonance imaging (MRI) of the brain and electroencephalogram (EEG) were normal, delaying diagnosis. LGI1 antibodies were later detected in his blood. He received corticosteroid treatment, showing cognitive improvement and a decrease in the number of confusion episodes. The patient's family stated that the spasms were improved after treatment. This case highlights the need for early testing and treatment, even when initial findings are normal.
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Taxonomy
TopicsAutoimmune Neurological Disorders and Treatments · Peripheral Neuropathies and Disorders · Cellular transport and secretion
