Related Experiment Video
Updated: Apr 2, 2026

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
Alternative diagnoses in patients referred to neuroimmunology for autoimmune encephalitis evaluation
Sophia F Damman1, Samhitha M Rai1, Rajeet Shrestha1,2
1Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Objective:
To evaluate alternative diagnoses in patients referred to neuroimmunology for evaluation of autoimmune encephalitis (AE) and/or positive neural antibodies.
Background:
With increased awareness of AE, AE misdiagnosis has increased-often from improper suspicion of AE or misinterpretation of clinically irrelevant neural antibodies.
Methods:
We retrospectively evaluated all cases referred to our center for AE evaluation and/or a positive neural antibody. We evaluated the frequency and characteristics of patients eventually diagnosed with an alternative diagnosis.
Results:
A total of 119 patients were referred between 2017 and 2024. Twenty-two were referred for a positive neural antibody, and seven for possible antibody-negative AE after testing negative before referral. Eighty-one patients1 were tested by our center after inpatient admission or outpatient referral. Our center deemed antibody testing unnecessary in 9 patients. Overall, 74 patients were antibody-positive (62%). An alternative diagnosis was found in 60 patients (50.4%), including 32 with positive neural antibodies, and 28 antibody-negative patients. Of patients with alternative diagnoses, 22 had low-clinical-relevance antibodies: low-titer GAD65 (12), AchG (6), VGCC (5), and double-seronegative VGKC (4). Conversely, 10 had antibodies classically considered highly clinically relevant: high-titer GAD65 (4), GABA-BR (2), NMDAR (1), LGI-1 (1), CASPR2 (1), and GFAP (1). Of these, two had concurrent low-titer GAD65. The most common alternative diagnoses included other immune-mediated disorders (28.3%), somatic symptom disorder (23.3%), primary psychiatric disorders (11.7%), metabolic encephalopathy/myoclonus (5%), neurodegenerative disorders (5%), and at 3.3% each, Down syndrome regression disorder, genetic disorders, neuromuscular disorders, and posterior reversible encephalopathy syndrome.
Conclusion:
Alternative diagnoses are common in patients referred for AE evaluation and include mostly psychiatric and other autoimmune conditions. Alternative diagnoses are not restricted to patients with low-clinical-relevance neural antibodies-they are also seen in patients with high-clinical-relevance antibodies and antibody-negative patients.
More Related Videos
08:20Hippocampal Neuronal Cultures to Detect and Study New Pathogenic Antibodies Involved in Autoimmune Encephalitis
Published on: June 2, 2022
07:20A Simple Cell-based Immunofluorescence Assay to Detect Autoantibody Against the N-Methyl-D-Aspartate NMDA Receptor in Blood
Published on: January 9, 2018