Rhupus syndrome, a rare coexistence of systemic lupus erythematosus (SLE) and rheumatoid arthritis, is characterized by symmetrical erosive polyarthritis and permanent deformities in addition to the clinical and serological characteristics of SLE. Its prognosis is further complicated by neurological and hematological involvement, which dramatically lowers patients' perceptions of their quality of life in terms of their health. Rhupus individuals have significantly less kidney involvement than SLE patients do. We present a case of a young female who had symmetric, bilateral, erosive polyarthritis for one and a half years preceding the signs and symptoms of SLE, which occurred about six months later.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550206PMC
http://dx.doi.org/10.7759/cureus.29018DOI Listing

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Article Synopsis
  • - Rhupus is a rare syndrome that combines symptoms of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE), characterized by specific autoantibodies and erosive polyarthritis.
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  • - Results indicated a higher prevalence of certain HLA-DR types (HLA-DR1 and DR9) in rhupus patients compared to those with RA or SLE, suggesting potential for early identification of rhupus before an overlap diagnosis is made. *
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Article Synopsis
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  • Treatment with belimumab has shown promise, as evidenced by a case where the patient’s anti-CCP and anti-dsDNA antibody levels significantly decreased following treatment.
  • Measuring these antibody levels can be useful for diagnosing and monitoring treatment effectiveness in patients with Rhupus syndrome.
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