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Case report: successful treatment of posttransplant lymphoproliferative disorder and quiescence of dermatomyositis with rituximab and sirolimus.

Abstract
Posttransplant lymphoproliferative disorder (PTLD) remains one of the most important complications of intensive immunosuppressive therapy. A 65-year-old Caucasian woman received a primary en bloc kidney transplant from a deceased 2-year-old donor. After antithymocyte globulin induction she was treated with a maintenance regimen including cyclosporine and mycophenylate mofetil (MMF). She had a history of recurrent dermatomyositis, suggesting a flawed immune system. After a benign course for 9 months and after an increase in MMF from 2 to 3 g daily, she presented with pneumonia owing to Candida albicans, which was responsive to antibiotics, as was the PTLD. Persistent fever led to a diagnosis of PTLD. The immunosuppressive regimen was converted to sirolimus (SRL) and rituximab, with over 90% necrosis of the neoplasm at 1 month. However, owing to concern at exploration, the allografts were extirpated. This case documented the benefit of the rituximab-SRL combination to treat PTLD while maintaining dermatomyositis in remission.
AuthorsZ Kaposztas, W B Etheridge, B D Kahan
JournalTransplantation proceedings (Transplant Proc) Vol. 40 Issue 5 Pg. 1744-6 (Jun 2008) ISSN: 0041-1345 [Print] United States
PMID18589184 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Immunosuppressive Agents
  • Rituximab
  • Sirolimus
Topics
  • Aged
  • Antibodies, Monoclonal (therapeutic use)
  • Antibodies, Monoclonal, Murine-Derived
  • Appendectomy
  • Child, Preschool
  • Dermatomyositis (drug therapy, surgery)
  • Female
  • Humans
  • Immunosuppressive Agents (adverse effects, therapeutic use)
  • Kidney Function Tests
  • Kidney Transplantation (adverse effects, immunology, physiology)
  • Lymphoproliferative Disorders (drug therapy)
  • Ovariectomy
  • Postoperative Complications (drug therapy)
  • Rituximab
  • Sirolimus (therapeutic use)

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