首页> 外文期刊>Case Reports in Rheumatology >Systemic Lupus Erythematosus (SLE) and Antineutrophil Cytoplasmic Antibody-Associated Vasculitis (AAV) Overlap Syndrome: Case Report and Review of the Literature
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Systemic Lupus Erythematosus (SLE) and Antineutrophil Cytoplasmic Antibody-Associated Vasculitis (AAV) Overlap Syndrome: Case Report and Review of the Literature

机译:全身狼疮红斑(SLE)和抗嗜酸性能细胞质抗体相关的血管炎(AAV)重叠综合征:病例报告和文献审查

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摘要

We report here the first case of systemic lupus erythematosus (SLE) and antineutrophil cytoplasmic antibody-associated vasculitis overlap syndrome (SLE/AAV) who had granulomatous polyangiitis (GPA) as the initial presentation. SLE/AAV overlap syndrome is an uncommon entity recently described in the literature. Prior reported patients with SLE/AAV overlap syndrome presented with SLE and microscopic polyangiitis (MPA). Our patient initially presented with granulomatous gastric ulcer and later developed respiratory failure. She was diagnosed with GPA. While on maintenance treatment with azathioprine 150?mg/day, she developed hematuria and proteinuria which turned out to be from class V lupus nephritis instead of relapse of vasculitis. Currently, the patient is doing well after treatment with rituximab. Although rare, this entity should be recognized and need to be treated appropriately.
机译:我们在此报告系统性狼疮性红斑(SLE)和抗替托利耳菌细胞质抗体相关血管炎重叠综合征(SLE / AAV)作为初始介绍。 SLE / AAV重叠综合征是最近在文献中描述的罕见实体。先前报道的SLE / AAV重叠综合征患者呈现为SLE和微观多阳炎(MPA)。我们的患者最初呈现肉芽肿胃溃疡,后来发育呼吸衰竭。她被诊断出患有GPA。虽然用杜鹃花素维持治疗150?mg /天,她开发出血尿和蛋白尿,结果来自V级狼疮肾炎而不是血管炎复发。目前,患者在用Rituximab治疗后表现良好。虽然罕见,但应识别这个实体,并需要适当对待。

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