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      Successful treatment of thrombotic microangiopathy after haematopoietic stem cell transplantation with rituximab.

      British Journal of Haematology
      ADAM Proteins, immunology, Adult, Antibodies, Monoclonal, therapeutic use, Antibodies, Monoclonal, Murine-Derived, Autoantigens, blood, Biological Markers, Female, Glucocorticoids, Hematopoietic Stem Cell Transplantation, adverse effects, Humans, Immunologic Factors, Infant, Male, Microcirculation, Middle Aged, Plasma Exchange, Prednisolone, Remission Induction, Retrospective Studies, Thrombosis, drug therapy, etiology, therapy, Treatment Outcome

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          Abstract

          Thrombotic microangiopathy (TMA) is a grave complication after haematopoietic stem cell transplantation (HSCT) and effective treatment is undefined. Five patients with postHSCT TMA, which was refractory to at least 1 week of plasma exchange and prednisolone, were treated with rituximab (375 mg/m(2)/week x 4). Remission was achieved in four patients, of whom three remained in remission and one had died of sepsis at a median follow-up of 10 months. ADAMTS13 levels were low in all evaluable patients, and only one patient showed significant anti-ADAMTS13 antibody. The levels of ADAMTS13 and anti-ADAMTS13 antibody did not change significantly with rituximab-induced remission.

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