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纯红细胞再生障碍和免疫性血小板减少症合并系统性红斑狼疮病例:利妥昔单抗和环磷酰胺的疗效。

A case of pure red cell aplasia and immune thrombocytopenia complicating systemic lupus erythematosus: response to rituximab and cyclophosphamide.

机构信息

Department of Rheumatology, University College Hospital, London, UK.

出版信息

Lupus. 2011 Dec;20(14):1547-50. doi: 10.1177/0961203311411349. Epub 2011 Oct 12.

Abstract

Pure red cell aplasia (PRCA) is a recognized but rare complication of systemic lupus erythematosus (SLE) and is characterized by the near absence of red blood cell precursors in the bone marrow but with normal megakaryocyte and granulocytes. We report a novel case of acquired PRCA occurring simultaneously with immune thrombocytopenia in the context of active SLE. Both syndromes were refractory to conventional treatment but responded to rituximab and cyclophosphamide.

摘要

纯红细胞再生障碍性贫血 (PRCA) 是系统性红斑狼疮 (SLE) 的一种公认但罕见的并发症,其特征是骨髓中几乎不存在红细胞前体,但巨核细胞和粒细胞正常。我们报告了一例新的获得性 PRCA 病例,该病例同时发生在活动期 SLE 合并免疫性血小板减少症的情况下。两种综合征均对常规治疗无效,但对利妥昔单抗和环磷酰胺有反应。

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