Division of Rheumatology, Hospital for Special Surgery, Weill Medical College of Cornell University, NY 10021, USA.
Curr Rheumatol Rep. 2011 Aug;13(4):291-9. doi: 10.1007/s11926-011-0179-5.
Anemia, leukopenia, and/or thrombocytopenia can occur as a result of non-immune- and immune-mediated mechanisms in patients with systemic lupus erythematosus. Although the differential diagnosis of these cytopenias is broad and warrants a thorough evaluation, lupus disease activity and medications are common etiologic factors. Corticosteroids are the mainstay of initial treatment for immune-mediated hemolytic anemia and severe thrombocytopenia; immunosuppressive agents such as mycophenolate mofetil or azathioprine are often added for their steroid-sparing effects. Rituximab and intravenous immunoglobulin can be considered for refractory cytopenias based on a large body of anecdotal evidence and case series. Newer biologic agents such as belimumab or epratuzumab have yet to be studied specifically in systemic lupus erythematosus-mediated hematologic disorders.
贫血、白细胞减少和/或血小板减少可由于系统性红斑狼疮患者的非免疫和免疫介导机制引起。虽然这些血细胞减少症的鉴别诊断广泛,需要进行彻底评估,但狼疮疾病活动和药物是常见的病因因素。皮质类固醇是治疗免疫介导性溶血性贫血和严重血小板减少症的主要药物;为了节省类固醇的作用,通常会添加免疫抑制剂,如霉酚酸酯或硫唑嘌呤。根据大量的传闻证据和病例系列,利妥昔单抗和静脉注射免疫球蛋白可用于治疗难治性血细胞减少症。新型生物制剂,如贝利尤单抗或依鲁替尼,尚未专门针对系统性红斑狼疮引起的血液系统疾病进行研究。