Navigating Rhupus Complexity

    Dilara Bulut Gökten, Rıdvan Mercan
    Studysummary This case report details a 42-year-old woman with Rhupus, a rare overlap syndrome of rheumatoid arthritis and systemic lupus erythematosus, emphasizing diagnostic challenges due to non-specific clinical criteria and documenting symptoms like inflammatory arthritis, malar rash, and hematological abnormalities.
    Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
    Rhupus is a rare syndrome characterized by the overlap of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE), with only about 60 cases documented in the literature. This case study discusses a 42-year-old female patient with Rhupus who exhibited symptoms such as inflammatory arthritis, bilateral wrist swelling, severe malar rash, oral ulcers, alopecia, anemia, and thrombocytopenia. Her laboratory results showed elevated erythrocyte sedimentation rate and decreased hemoglobin and platelet count. The case highlights the diagnostic challenges due to the lack of well-defined clinical criteria and aims to contribute to the understanding of this complex syndrome.
    Discuss this study in the Community →