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Idiopathic lung fibrosis and anti myeloperoxidase glomerulonephritis: the tree that hides the forest

机译:特发性肺纤维化和抗髓过氧化物酶肾小球肾炎:掩盖森林的树

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Although anti-neutrophil cytoplasmic antibodies [ANCA] are frequently found in patients diagnosed with idiopathic pulmonary fibrosis [IPF], current guidance does not recommend serologic testing for vasculitis. A 71-year old Caucasian male, diagnosed with IPF three years earlier, presented with rapidly progressive glomerulonephritis. ANCA were found both in current and historical sera. A kidney biopsy sample was taken, which revealed a pauci-immune glomerulonephritis, but also areas of glomerular fibrosis, hence strongly suggesting unrecognized flares of an indolent vasculitis in his past. This made the diagnosis of “idiopathic” pulmonary fibrosis very unlikely. As nephrologists, we argue that testing for ANCA should be performed on a systematic basis, at least in elderly patients, even in the absence of extra-pulmonary signs of vasculitis at presentation.
机译:尽管在诊断为特发性肺纤维化[IPF]的患者中经常发现抗中性粒细胞胞浆抗体[ANCA],但当前指南不建议对血管炎进行血清学检测。一名71岁的白人男性,三年前被诊断出IPF,表现为快速进行性肾小球肾炎。在当前和历史血清中都发现了ANCA。取肾活检标本,显示出免疫球蛋白免疫性的肾小球肾炎,以及肾小球纤维化的区域,因此强烈暗示了过去未曾发现的惰性血管炎的发作。这使得诊断“特发性”肺纤维化的可能性非常小。作为肾病学家,我们认为应至少在老年患者中系统地进行ANCA测试,即使在没有肺外血管炎迹象的情况下也是如此。

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