Think

When to Suspect Autoimmune Encephalitis

Clinical Presentation

Onset

Acute to subacute progressive neuropsychiatric presentation. It is important to note that some types of AIE can present with a chronic course including AIE associated with: Anti-LGI1 Ab, Anti-CASPR2 Ab, Anti-DPPX Ab or Anti-IgLON5 Ab.  

Prodromal symptoms

Infectious​​​ prodrome days to weeks preceding neuropsychiatric​​​ presentation. Other non-specific symptoms including headache, fatigue, sleep, weight loss & early psychiatric manifestations

Risk Factors

Personal or family history of autoimmune diseases, infectious encephalitis and immune checkpoint inhibitors treatment


Once AIE diagnosis is suspected, physicians should

Obtain evidence supporting the diagnosis

By completing the recommended investigations in the link below

Click here

Exclude mimics

Review a broad spectrum of conditions that can mimic autoimmune encephalitis by visiting the link below to read the following article: "Autoimmune Encephalitis Misdiagnosis in Adults" *

* This is intended as a general overview and does not cover all possible mimics.

Click here