Clinical Features of Children With Anti-N-Methyl-D-Aspartate Receptor Encephalitis Following Viral Encephalitis

Vu Thi Minh Phuong1,2, Phung Thi Bich Thuy1,3, Dao Huu Nam2

  • 1Department of Pediatrics, Hanoi Medical University, Hanoi, Vietnam.

Insights

Anti-N-methyl-D-aspartate receptor encephalitis (anti-NMDARE) can follow viral encephalitis. Children with anti-NMDARE after herpes simplex encephalitis or Japanese encephalitis often develop movement disorders and psychiatric symptoms.

Area of Science:

  • Neurology
  • Pediatrics
  • Immunology

Background:

  • Anti-N-methyl-D-aspartate receptor encephalitis (anti-NMDARE) is a recognized complication following viral encephalitis, including herpes simplex encephalitis (HSE) and Japanese encephalitis (JE).
  • Understanding the distinct clinical presentations and outcomes of anti-NMDARE post-viral encephalitis in children is crucial for timely diagnosis and management.

Purpose of the Study:

  • To delineate the clinical characteristics, laboratory findings, and treatment outcomes of pediatric patients experiencing anti-NMDARE subsequent to viral encephalitis.
  • To compare the clinical and laboratory features between the initial viral encephalitis phase and the subsequent anti-NMDARE phase.

Main Methods:

  • A retrospective case series involving 14 children diagnosed with anti-NMDARE following viral encephalitis (HSE or JE) between January 2021 and December 2022.
  • Exclusion criteria included evidence of viral reactivation or other specific antibodies to ensure focus on anti-NMDARE post-viral encephalitis.

Main Results:

  • The majority of patients (12/14) developed anti-NMDARE after HSE. Common initial symptoms included fever and seizures, with no movement disorders or psychiatric symptoms. Post-anti-NMDARE, movement disorders (92.9%), fever (71.4%), sleep disturbances (64.3%), seizures (50%), and psychiatric symptoms (50%) were prevalent.
  • Cerebrospinal fluid (CSF) analysis showed variations between phases, with a higher protein concentration during the anti-NMDARE phase (0.85 ± 0.63 g/L) compared to the viral encephalitis phase (0.43 ± 0.16 g/L).
  • Brain MRI scans in 10 patients revealed no new lesions in 8 cases, suggesting limited structural changes despite distinct clinical manifestations.

Conclusions:

  • Significant differences exist in clinical symptoms and CSF findings between viral encephalitis and subsequent anti-NMDARE phases in children.
  • Despite the distinct clinical evolution, most pediatric patients in this cohort did not exhibit new brain lesions on MRI, highlighting the importance of clinical and CSF findings for diagnosis.
Abstract