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Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab.

Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab. Research Abstract Details 

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  • Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab. Abstract Text:

    shinichi kakoShinichi Kako,yoshinobu kandaYoshinobu Kanda,kumi oshimaKumi Oshima,nahoko nishimotoNahoko Nishimoto,hiroyuki satoHiroyuki Sato,takuro watanabeTakuro Watanabe,noriko hosoyaNoriko Hosoya,toru motokuraToru Motokura,shigesaburo miyakoshiShigesaburo Miyakoshi,shuichi taniguchiShuichi Taniguchi,aki kamijoAki Kamijo,koki takahashiKoki Takahashi,shigeru chibaShigeru Chiba,mineo kurokawaMineo Kurokawa,

    Hemolytic anemia and pure red cell aplasia (PRCA) after allogeneic hematopoietic stem cell transplantation (HSCT) have been reported to be mainly related to ABO-incompatibility between donor and recipient. Autoimmune hemolytic anemia (AIHA) without ABO-incompatibility has been also reported after allogeneic HSCT, especially with T-cell depletion. However, optimal management of AIHA or PRCA remains unclear. A 54-year-old male with myelodysplastic syndrome (MDS) underwent haploidentical human leukocyte antigen-mismatched HSCT using in vivo alemtuzumab and developed AIHA and PRCA simultaneously 15 months after transplantation, following the administration of cidofovir and probenecid for persistent cytomegalovirus (CMV) antigenemia and retinitis. AIHA was successfully treated with rituximab, and subsequently PRCA with cyclosporine without relapse of MDS or recurrence of CMV infection. The clinical course suggested that AIHA was mainly caused by humoral immune response, while PRCA was mainly caused by cell-mediated immune response in this patient, although these immune responses might be related to each other. Am. J. Hematol., 2008. (c) 2007 Wiley-Liss, Inc.

    Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab. Publishing Authors By Initials

    s kakoS Kako,y kandaY Kanda,k oshimaK Oshima,n nishimotoN Nishimoto,h satoH Sato,t watanabeT Watanabe,n hosoyaN Hosoya,t motokuraT Motokura,s miyakoshiS Miyakoshi,s taniguchiS Taniguchi,a kamijoA Kamijo,k takahashiK Takahashi,s chibaS Chiba,m kurokawaM Kurokawa,

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    Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: American journal of hematology

    VOLUME: 83

    Page Numbers: 247-9

    Journal Abbreviation: Am. J. Hematol.

    ISSN: 0361-8609

    DAY: 4

    MONTH: Mar

    YEAR: 2008

    Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab. Information

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    LANGUAGE: eng

    NlmUniqueID: 7610369

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    Grant and Affiliation Information for Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab.

    AFFILIATION: Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Am J Hematol

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