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首页> 外文期刊>Saudi journal of kidney diseases and transplantation : >An overlap of granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis
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An overlap of granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis

机译:肉芽肿病与多苯炎和嗜酸性粒细胞芽孢杆菌与多苯炎重叠

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We present a case report of overlap of granulomatosis with polyangiitis (GPA; formerly known as Wegener’s granulomatosis) and eosinophilic granulomatosis with polyangiitis (EGPA; formerly known as Churg-Strauss syndrome). We report a 45-year-old female who presented with rapidly progressive renal failure associated with fever, polyarthralgia, and respiratory symptoms with cytoplasmic antineutrophilic cytoplasmic antibody (ANCA) and proteinase (PR-3) antigen positivity. Computerized tomography scan of the chest showed diffuse alveolar hemorrhage with renal biopsy revealing pauci-immune necrotizing crescentic glomerulonephritis with intense eosinophilic infiltration suggestive of eosinophilic GPA (EGPA). Our patient had ANCA-associated vasculitis (AAV) with features suggestive of both GPA and EGPA. She was treated with methylprednisolone and cyclophosphamide and attained remission after 2 weeks of therapy. This is a rare report of a patient with AAV having features of both EGPA and GPA.
机译:我们展示了肉芽肿病的重叠案例报告,肉芽炎(GPA;以前称为Wegener的肉芽肿病)和嗜酸性粒细胞粒细胞瘤,具有多苯炎(EGPA;以前称为Churg-Strauss综合征)。我们报告了一名45岁的女性,伴随着与发烧,多次曲线和呼吸症状有关的迅速进行的肾功能衰竭,具有细胞质抗癌性细胞质抗体(ANCA)和蛋白酶(PR-3)抗原阳性。胸部的电脑断层扫描显示弥漫性肺泡出血与肾脏活检揭示了嗜酸性嗜酸性GPA(EGPA)的强烈嗜酸性渗透性的益生菌性肺炎肾小球肾炎。我们的患者具有ANCA相关的血管炎(AAV),具有暗示GPA和EGPA的特征。她用甲基己酮龙和环磷酰胺治疗,治疗2周后达到缓解。这是具有AAV具有EGPA和GPA的特征的患者的罕见报告。

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