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Successful rituximab treatment of refractory hemophagocytic lymphohistiocytosis and autoimmune hemolytic anemia associated with systemic lupus erythematosus

机译:利妥昔单抗成功治疗难治性吞噬性淋巴细胞组织细胞增生和自身免疫性溶血性贫血伴系统性红斑狼疮

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摘要

High-dose steroids, immunosuppressants such as cyclophosphamide and cyclosporine, and high-dose intravenous immunoglobulin have all been used to control hemophagocytic lymphohistiocytosis (HLH) or autoimmune hemolytic anemia (AIHA) associated with systemic lupus erythematosus (SLE); however, some patients are refractory to treatment. Rituximab has successfully resolved many of the refractory manifestations of SLE. Here, we report a case of HLH and AIHA associated with SLE that was refractory or intolerable to conventional therapy, but was successfully treated with rituximab.
机译:大剂量的类固醇,免疫抑制剂(例如环磷酰胺和环孢素)以及大剂量的静脉注射免疫球蛋白已被用于控制与系统性红斑狼疮(SLE)相关的吞噬性淋巴细胞组织细胞增生症(HLH)或自身免疫性溶血性贫血(AIHA);但是,有些患者无法接受治疗。利妥昔单抗已成功解决了SLE的许多难治性表现。在这里,我们报告了与SLE相关的HLH和AIHA病例,对常规治疗是难治性或不能耐受的,但已成功用利妥昔单抗治疗。

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