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Published on: July 4, 2007
Progressive multifocal leukoencephalopathy following rituximab treatment in a patient with rheumatoid arthritis
1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX 75231, USA. rfleischmann@arthdocs.com
Abstract:
Progressive multifocal leukoencephalopathy (PML) is a rare brain disease caused by reactivation of the JC virus. Herein, a case of PML in association with rituximab treatment in a patient with chronic rheumatoid arthritis (RA) and Sjögren's syndrome is described. The patient received 4 courses of rituximab (2 1,000-mg infusions administered 2 weeks apart) over a period of approximately 40 months, during a phase III trial and safety extension study. PML was diagnosed approximately 18 months after the last rituximab course, and the patient died 1 month later. Determination of the cause of PML was confounded by the fact that the patient had developed oropharyngeal cancer, which was treated with chemoradiotherapy, 9 months prior to the development of PML. Although there was no direct evidence that linked rituximab to the development of PML, this case highlights the need to consider a diagnosis of PML in patients with RA who have been treated with rituximab and who subsequently develop new neurologic symptoms.
Insights
Progressive multifocal leukoencephalopathy (PML), a rare brain disease, was observed in a rheumatoid arthritis patient after rituximab treatment. This case underscores the importance of considering PML in patients with new neurological symptoms post-treatment.
Area of Science:
- Neuroimmunology
- Rheumatology
- Oncology
Background:
- Progressive multifocal leukoencephalopathy (PML) is a rare, fatal demyelinating disease of the central nervous system.
- JC virus (JCV) reactivation is the causative agent of PML.
- Rituximab, a monoclonal antibody, is used to treat autoimmune diseases like rheumatoid arthritis (RA) and Sjögren's syndrome.
Observation:
- A case of PML is described in a patient with chronic rheumatoid arthritis and Sjögren's syndrome.
- The patient received multiple courses of rituximab over approximately 40 months.
- PML diagnosis occurred 18 months after the last rituximab course, with subsequent mortality.
Findings:
- The patient developed oropharyngeal cancer and received chemoradiotherapy 9 months prior to PML diagnosis, complicating etiological determination.
- No direct evidence linked rituximab to PML development in this specific case.
- Neurological symptoms arose approximately 18 months post-rituximab therapy.
Implications:
- This case highlights the potential need to consider PML in rheumatoid arthritis patients treated with rituximab who develop new neurological symptoms.
- Further research is warranted to elucidate the precise relationship between rituximab, underlying autoimmune conditions, and PML risk.
- Early recognition and diagnosis of PML are critical for patient management, despite treatment complexities.
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