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Anti-NMDAR Encephalitis With Serial Negative MRI Findings: An Evaluation Using Autoimmune Psychosis Criteria.

Satoshi Saito, Go Taniguchi, Chihiro Nakata, Hideo Kato, Mao Otake, Masahiro Umeda, Yuichiro Fuji, Eiji Nakagawa

Case reports in neurological medicine January 1, 2025 DOI: 10.1155/crnm/4561447 via PubMed

Summary

AI-generated from the abstract

A 15-year-old boy with sudden seizures and worsening psychiatric symptoms—including reduced reactivity, language deterioration, and catatonia—was initially misdiagnosed with a psychiatric disorder because repeated MRI scans were normal. Using autoimmune psychosis criteria, doctors suspected autoimmune encephalitis, which was confirmed by detecting oligoclonal bands and anti-NMDAR antibodies in blood and spinal fluid. Steroid pulse therapy led to significant improvement. The case shows that anti-NMDAR encephalitis can mimic primary psychiatric conditions and that autoimmune psychosis criteria, which consider features like subacute onset, catatonia, cognitive dysfunction, altered consciousness, and seizures, can aid diagnosis even when standard biomarkers are negative.

Study at a glance

Characteristics Case study Case report Peer reviewed
Sample size 1
Population 15-year-old male with anti-NMDAR encephalitis
Intervention steroid pulse therapy
Topics Altered states of consciousness
Keywords Electroencephalography Levetiracetam Peri-ictal psychosis Diagnostic testing
Key finding Autoimmune psychosis criteria correctly identified anti-NMDAR encephalitis in a patient with negative MRI and CSF findings, leading to effective treatment with steroids.

Abstract

Autoimmune psychosis criteria have been proposed for autoimmune encephalitis with prominent psychiatric symptoms as an alternative to biomarker-based diagnostic approaches such as the Graus criteria. We present a case of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis that was initially misdiagnosed as a psychiatric disorder due to serial negative MRI findings and subsequently re-evaluated correctly using autoimmune psychosis criteria. A 15-year-old male developed sudden-onset generalized convulsive seizures that increased progressively in frequency and fluctuating psychiatric symptoms that gradually worsened to include reduced reactivity, language deterioration, and catatonia. On admission, both brain MRI and cerebral spinal fluid (CSF) findings were unremarkable; however, autoimmune encephalitis was strongly suspected based on autoimmune psychosis criteria and subsequently confirmed by detection of oligoclonal bands (OCBs) and anti-NMDAR antibodies in the serum and CSF. Repeated steroid pulse therapy resulted in significant clinical improvement. The patient met multiple autoimmune psychosis criteria, including subacute onset of psychiatric symptoms, catatonia, disproportionate cognitive dysfunction, decreased level of consciousness, and the emergence of seizures. These features are not typically present in primary psychiatric disorders. Anti-NMDAR encephalitis can present with a variety of symptoms, complicating its differentiation from primary psychiatric conditions. The application of autoimmune psychosis criteria may serve as a valuable diagnostic aid, particularly when MRI findings are repeatedly negative.

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