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Rituximab as a Treatment Option after Autologous Hematopoietic Stem Cell Transplantation in a Patient with Systemic Sclerosis. | LitMetric

AI Article Synopsis

  • Systemic sclerosis (SSc) is a tough autoimmune disease that leads to blood vessel problems and organ scarring, and autologous hematopoietic stem cell transplantation (AHSCT) can help high-risk patients.
  • A 43-year-old man with severe SSc underwent AHSCT but continued to experience heart issues, prompting the use of the drug rituximab (RTX) eight months later.
  • After starting RTX, the patient's symptoms and organ functions significantly improved, showcasing that RTX may be a beneficial treatment for SSc patients who do not respond to AHSCT.

Article Abstract

Systemic sclerosis (SSc) is an intractable autoimmune disease characterized by vasculopathy and organ fibrosis. Autologous hematopoietic stem cell transplantation (AHSCT) should be considered for the treatment of selected patients with rapid progressive SSc at high risk of organ failure. It, however, remains elusive whether immunosuppressive therapies such as rituximab (RTX) are still necessary for such patients after AHSCT, especially in those with bad outcomes. In the present report, a 43-year-old man with diffuse cutaneous SSc received AHSCT. Despite AHSCT, SSc further progressed with progressive symptomatic heart failure with newly developed concomitant mitral and tricuspid valve insufficiency, thus the patient started on RTX 8 months after AHSCT. Shortly after initiation of RTX, clinical symptoms and organ functions ameliorated subsequently. Heart valve regurgitations were reversible after initiation of RTX treatment. Currently, the patient remains in a stable condition with significant improvement of clinical symptoms and organ functions. Reporting about therapies after AHSCT in SSc is a very important issue, as randomized controlled trials are lacking, and therefore this report adds to evidence that RTX can be considered as a treatment option in patients with SSc that do not respond to AHSCT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305780PMC
http://dx.doi.org/10.3390/jpm11070600DOI Listing

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