Enterovirus A71 causing meningoencephalitis and acute flaccid myelitis in a patient receiving rituximab

Ronak K Kapadia1, Christine M Gill2, Christine Baca3

  • 1Neuro-Infectious Diseases Group, Department of Neurology, Division of Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, United States of America; Department of Neurology, University of Colorado, Aurora, CO, United States of America; Division of Neurology, Department of Clinical Neurosciences, University of Calgary, Cummings School of Medicine, Calgary, Alberta, Canada.

Insights

A young woman on rituximab for rheumatoid arthritis developed severe enteroviral meningoencephalitis and acute flaccid myelitis (AFM). Prompt diagnosis and treatment with IVIg and fluoxetine led to remarkable recovery, highlighting EV-A71 risks in immunosuppressed patients.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Immunology

Background:

  • Rituximab is an immunosuppressive therapy used for rheumatoid arthritis.
  • Enteroviral infections can cause severe neurological complications, including meningoencephalitis and acute flaccid myelitis (AFM).
  • Enterovirus A71 (EV-A71) is a known neurotropic pathogen.

Observation:

  • A young woman undergoing rituximab treatment for rheumatoid arthritis presented with severe meningoencephalitis and AFM.
  • Cerebrospinal fluid (CSF) and stool samples confirmed enteroviral infection, identified as EV-A71 by CDC sequencing.
  • The patient received intravenous immunoglobulin (IVIg) and fluoxetine for treatment.

Findings:

  • The patient experienced a significant clinical improvement following IVIg and fluoxetine therapy.
  • This case demonstrates a potential clinical presentation and recovery course for enteroviral meningoencephalitis and AFM in an immunosuppressed individual.
  • Diagnostic confirmation relied on RT-PCR testing of CSF and stool, underscoring the importance of multi-site testing.

Implications:

  • This case underscores the critical need to consider enteroviral infections in patients receiving rituximab therapy.
  • It highlights the potential severity of EV-A71 neurological disease and suggests a possible therapeutic approach.
  • Emphasizes the diagnostic value of testing multiple biological samples (CSF, stool, nasopharyngeal swab, blood) for enterovirus detection.

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