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Published on: July 4, 2007
[Progressive multifocal leukoencephalopathy in a patient with rheumatoid arthritis under salazosulfapyridine
Tomoko Okazaki1, Daichi Kodama1, Misaki Yamadera2
1Department of Neurology, Osaka Police Hospital.
Abstract:
Progressive multifocal leukoencephalopathy (PML) is a rare opportunistic infection caused by JC virus (JCV) activation. We report an 85-years old man who had been diagnosed to have rheumatoid arthritis (RA) 1.5 years prior to diagnosis of PML, and had been treated with salazosulfapyridine (SASP). He developed weakness of the left upper limb, which progressed gradually for two months. A neurological examination on admission revealed severe palsy of the left upper limb without sensory disturbance, cognitive decline or gait disturbance. Brain MRI revealed white matter lesions in the right frontal lobe around the precentral gyrus. Cerebrospinal fluid (CSF) examination and peripheral lymphocyte counts were normal. HIV was ruled out serologically. There were no findings suggestive of malignancy. We suspected PML and stopped SASP. JCV-DNA was detected in CSF. There were enlarged nuclei positive with VP-1 immunostaining in the brain biopsy materials. Thus, the diagnosis of PML was definitive. Paralysis of the left upper limb began to improve one week after discontinuing SASP. Treatment with mefloquine and mirtazapine was initiated, but he developed severe interstitial pneumonia, which might be caused by mefloquine. Therefore, he underwent rehabilitation without medication. JCV-DNA became undetectable and white matter lesions decreased 6 months later. Paralysis improved and he had no problem with activities of daily living a year later. The risk factor for PML has changed over the last decade, and drugs such as biologics became significant risk factors for patients with autoimmune diseases. There are reports suggesting that systemic lupus erythematosus (SLE) and RA themselves might be independent risk factors for PML. Although there is no previous report of SASP inducing PML, SASP might be the culprit in our case. However, there is another possibility that SAPS and RA worked synergistically for the onset of PML.
Insights
This case study highlights a rare instance of progressive multifocal leukoencephalopathy (PML) in an 85-year-old man treated for rheumatoid arthritis (RA). The patient recovered significantly after discontinuing salazosulfapyridine (SASP), suggesting a potential link between the drug, RA, and PML.
Area of Science:
- Neurology
- Immunology
- Infectious Diseases
Background:
- Progressive multifocal leukoencephalopathy (PML) is a rare, often fatal, opportunistic infection caused by the JC virus (JCV).
- Risk factors for PML have evolved, with immunosuppressive therapies for autoimmune diseases like rheumatoid arthritis (RA) becoming increasingly significant.
- The role of specific medications, such as salazosulfapyridine (SASP), in inducing PML remains under investigation.
Observation:
- An 85-year-old male with a history of RA treated with SASP presented with progressive left upper limb weakness.
- Neurological examination revealed severe left upper limb palsy; MRI showed white matter lesions in the right frontal lobe.
- Cerebrospinal fluid (CSF) and peripheral lymphocyte counts were normal, and HIV was ruled out.
Findings:
- JC virus DNA (JCV-DNA) was detected in the CSF, and brain biopsy confirmed PML.
- Discontinuation of SASP led to improvement in limb paralysis within a week.
- While mefloquine and mirtazapine were initiated, severe interstitial pneumonia possibly related to mefloquine necessitated their cessation.
Implications:
- This case suggests a potential association between SASP use and PML development, possibly in synergy with RA.
- The findings underscore the importance of considering PML in patients with autoimmune diseases on immunosuppressive therapy, even with atypical drug associations.
- Successful management through drug withdrawal and rehabilitation highlights the potential for recovery in PML, emphasizing early diagnosis and intervention.
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