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Diffuse Alveolar Hemorrhage Emerging One Week after Starting High-dose Corticosteroid Therapy for Granulomatosis with Polyangiitis (GPA) with Systemic Lupus Erythematosus (SLE)

机译:大剂量糖皮质激素治疗肉芽肿伴多血管炎(Gpa)伴系统性红斑狼疮(sLE)一周后出现弥漫性肺泡出血

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摘要

A 69-year-old man was diagnosed with granulomatosis with polyangiitis (GPA) based on the presence of skin granuloma, refractory otitis media, renal insufficiency and myeloperoxidase-antineutrophil cytoplasmic antibody positivity and slight lung opacity. He was treated with high-dose corticosteroid therapy. Despite the initial improvement of his renal function and a decrease in his C-reactive protein level, he suffered from an alveolar hemorrhage one week after the start of corticosteroid therapy. An anti-dsDNA antibody test was positive and the patient had hypocomplementemia. Elements of both GPA and systemic lupus erythematosus were thought to have affected his clinical course.
机译:基于皮肤肉芽肿,难治性中耳炎,肾功能不全和髓过氧化物酶-抗中性粒细胞胞浆抗体阳性和轻微的肺部混浊,诊断为一名69岁男子患有肉芽肿性多血管炎(GPA)。他接受了大剂量皮质类固醇激素治疗。尽管肾功能最初有所改善,C反应蛋白水平有所下降,但在开始糖皮质激素治疗后一周,他仍患有肺泡出血。抗dsDNA抗体测试为阳性,患者患有低补体血症。 GPA和系统性红斑狼疮的元素都被认为影响了他的临床过程。

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