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Lupus Nephritis with Coexistent Antiphospholipid Antibodies Associated Nephropathy: A Case Report and Literature Review

机译:狼疮性肾炎合并抗磷脂抗体相关性肾病:一例报道并文献复习

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Antiphospholipid syndrome (APS) associated nephropathy is a distinct clinical entity and can occur in patients with systemic lupus erythematosus (SLE) independent of or associated with lupus nephritis. Associated APS nephropathy in a patient with lupus predicts poor renal outcome, especially if left untreated. Recognizing a coexistent APS nephropathy in a patient with lupus nephritis is of utmost importance. Here, we present a patient with severe lupus nephritis with antiphospholipid antibodies (aPLs) who had no thrombotic manifestations of APS clinically. On renal biopsy, she was found to have APS nephropathy. Remission was achieved after 3 months of anticoagulation and immunosuppression. This case illustrates the importance of renal biopsy in a patient of SLE with aPLs. Renal biopsy often alerts a treating rheumatologist of the presence of thrombotic involvement in such patients, thereby altering the treatment of such patients.
机译:抗磷脂综合征(APS)相关性肾病是一种独特的临床实体,可发生于系统性红斑狼疮(SLE)患者,独立于或伴发狼疮性肾炎。狼疮患者的相关性APS肾病预示肾预后不良,尤其是如果不及时治疗。识别狼疮性肾炎患者并存的APS肾病至关重要。在这里,我们介绍了一名患有抗磷脂抗体(aPLs)的重度狼疮肾炎患者,临床上没有APS的血栓形成表现。进行肾脏活检时,发现她患有APS肾病。 3个月的抗凝和免疫抑制后缓解。该病例说明了在患有aPL的SLE患者中进行肾活检的重要性。肾脏活检通常会提醒风湿病治疗专家此类患者存在血栓形成,从而改变此类患者的治疗方法。

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