| Literature DB >> 14686491 |
Abstract
A case is reported of idiopathic relapsed autoimmune hemolytic anemia successfully treated with rituximab. A 43-year-old white male patient with past medical history of Evans syndrome was found to have recurrent autoimmune hemolytic anemia. Previous treatments included steroids, splenectomy, intravenous immunoglobulin, plasmapheresis, staphylococcal Protein A immunoadsorption (Prosorba column), and chemotherapeutic agents (cytoxan and vincristine). Rituximab was given weekly at 375 mg/m2 for 4 doses. The drug was well tolerated and the patient remains in remission 9 months after completion of therapy.Entities:
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Year: 2003 PMID: 14686491 DOI: 10.1007/BF02983558
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490