肉芽肿伴多发性血管炎
医学
嗜酸性
抗中性粒细胞胞浆抗体
病理
显微镜下多血管炎
快速进行性肾小球肾炎
嗜酸性肺炎
弥漫性肺泡出血
血管炎
环磷酰胺
坏死性血管炎
甲基强的松龙
内科学
呼吸道疾病
化疗
肺
疾病
作者
Chandramohan Gundappa,Sujit Surendran,Arun Gandhi,Abraham Kurien,Edwin Fernando
标识
DOI:10.4103/1319-2442.206450
摘要
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.
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