Demyelinating disease (multiple sclerosis) in a patient with psoriatic arthritis treated with adalimumab: a case-based review.

Rheumatol Int

Division of Clinical Immunology and Rheumatology, Department of Internal Medicine, School of Medicine, University Hospital Center Zagreb, University of Zagreb, Zagreb, Croatia.

Published: December 2021

AI Article Synopsis

  • TNF-α inhibitors, like adalimumab, have become essential for treating psoriatic arthritis, but they can have unwanted side effects in some patients.
  • A patient with psoriasis, psoriatic arthritis, and uveitis developed symptoms of multiple sclerosis after 4 months of adalimumab treatment, despite having no prior neurological issues.
  • The case raises questions about whether the drug induced demyelination or simply revealed an underlying condition, highlighting the importance of monitoring side effects in clinical practice.

Article Abstract

Over the past two decades, tumor necrosis factor-α (TNF-α) inhibitors became one of the most important drugs in the treatment of patients with psoriatic arthritis. Unfortunately, some of the patients exhibit unwanted side effects of the treatment. We describe a patient with psoriasis, psoriatic arthritis and uveitis who was treated with adalimumab and after 4 months of the treatment developed clinical and neuroradiological signs of demyelinating disease of the central nervous system. She experienced no signs and symptoms of neurological disease prior to adalimumab administration. After a detailed neurological work-up she was diagnosed with relapsing-remitting type of multiple sclerosis and treated with oral and pulse glucocorticoids and later with dimethyl fumarate. Adalimumab was discontinued. The question remains was the demyelination induced by the TNF-α blockade or was it unmasked by the introduction of the cytokine blocking agent. In patients suffering from inflammatory arthritis, treating disease to target as well as a close follow-up and knowledge of potential side effects of treatment remains crucial in good clinical practice.

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Source
http://dx.doi.org/10.1007/s00296-021-04995-0DOI Listing

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