Department of Internal Medicine and Clinical Immunology, Dijon University Hospital, Dijon, France.
Intern Med J. 2012 Jan;42(1):95-8. doi: 10.1111/j.1445-5994.2011.02591.x.
Systemic lupus erythematosus (SLE) has been described as a cause of thrombotic microangiopathy, especially thrombotic thrombocytopenic purpura (TTP). Haemolytic-uraemic syndrome (HUS) is less frequent in SLE. We report a case of such an association during an episode of severe lupus nephritis in a young woman, who was successfully treated with steroids, cyclophosphamide and especially plasma exchange with plasma replacement. This report highlights the importance of recognising atypical HUS in SLE patients by looking for schistocytes in case of haemolytic anemia with a negative antiglobulin test, in order to begin plasma exchange.
系统性红斑狼疮(SLE)已被描述为血栓性微血管病的病因,尤其是血栓性血小板减少性紫癜(TTP)。溶血尿毒综合征(HUS)在 SLE 中较少见。我们报告了一例年轻女性在严重狼疮性肾炎发作期间出现这种关联的病例,该患者成功接受了类固醇、环磷酰胺治疗,特别是血浆置换联合血浆置换治疗。该报告强调了在出现溶血性贫血且抗球蛋白试验阴性时通过寻找裂体细胞来识别 SLE 患者非典型 HUS 的重要性,以便开始进行血浆置换。