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首页> 外文期刊>Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology >Successful treatment of refractory autoimmune hemolytic anemia with monthly rituximab following nonmyeloablative stem cell transplantation for sickle cell disease.
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Successful treatment of refractory autoimmune hemolytic anemia with monthly rituximab following nonmyeloablative stem cell transplantation for sickle cell disease.

机译:非清髓性干细胞移植治疗镰状细胞病后,每月使用利妥昔单抗成功治疗难治性自身免疫性溶血性贫血。

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摘要

Autoimmune hemolytic anemia (AIHA) can occur following hematopoietic stem cell transplantation (HSCT) and may be associated with other cytopenias. It can also occur in the context of chronic red cell transfusion in patients maintained on hypertransfusion regimens. There are an increasing number of reports on the successful treatment of autoimmune cytopenias with the monoclonal anti-CD20 antibody rituximab, including a few patients in a post-HSCT setting. The authors report the successful treatment with rituximab of refractory AIHA following allogeneic nonmyeloablative bone marrow transplantation in a child with sickle cell disease.
机译:自身免疫性溶血性贫血(AIHA)可能在造血干细胞移植(HSCT)之后发生,并可能与其他血细胞减少症相关。维持高输血方案的患者在慢性红细胞输注的情况下也可能发生这种情况。关于使用单克隆抗CD20抗体利妥昔单抗成功治疗自身免疫性血细胞减少症的报道越来越多,包括一些在HSCT后的患者。作者报告了在异基因非清髓性骨髓移植治疗镰状细胞病患儿后,利妥昔单抗治疗难治性AIHA成功。

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