Goodpasture’s Syndrome With Ambiguous Serology: A Case Report

J. Szczykowska, S. Brzósko, M. Rakowska, B. Naumnik
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引用次数: 1

Abstract

Pulmonary-renal syndrome is a rare clinical syndrome defined by a combination of diffuse alveolar hemorrhage and rapidly progressive crescentic glomerulonephritis. It is not a single entity, but is caused by a wide variety of diseases including Goodpasture’s syndrome associated with autoantibodies against glomerular and alveolar basement membrane (anti-glomerular basement membrane (anti-GBM)). Anti-GBM disease is an autoimmune disorder, estimated to occur in less than one case per million population. A 59-year-old previously healthy man presented with acute kidney injury (AKI, stage 3, KDIGO) with signs of nephritic syndrome, progressive oliguria, dyspnea with mild hemoptysis, cruses edema and elevated blood pressure. Serologic results were all negative except very low titer of anti-proteinase 3 antibodies. Chest radiograph revealed diffuse pulmonary infiltrations. Renal biopsy demonstrated necrotizing crescentic glomerulonephritis with linear pattern for immunoglobulin G along the entire GBM in immunofluorescent staining. Based on whole clinical picture, the diagnosis of Goodpasture’s syndrome was done and the intensive treatment, including plasmapheresis, cyclophosphamide and prednisone, along with hemodialysis was provided. Improvement of patient’s general condition was achieved. Despite recovery of diuresis, attempt to discontinue hemodialysis was found unsuccessful. The case proves the importance of diagnostic vigilance in patients presenting with AKI. Although supportive, in many cases, serology tests can be negative or ambiguous and should not prevent profound diagnostic process including kidney biopsy. Late diagnosis in the course of anti-GBM disease, in spite of proper treatment, correlates with less favorable kidney outcomes. World J Nephrol Urol. 2017;6(1-2):10-13 doi: https://doi.org/10.14740/wjnu301w
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Goodpaste综合征伴血清学不清1例报告
肺肾综合征是一种罕见的临床综合征,由弥漫性肺泡出血和快速进行性新月体肾小球肾炎合并引起。它不是一个单一的实体,而是由多种疾病引起的,包括与肾小球和肺泡基底膜自身抗体(抗肾小球基底膜(抗GBM))相关的Goodpaste综合征。抗GBM疾病是一种自身免疫性疾病,估计每百万人口中发生的病例不到一例。一名59岁的健康男性出现急性肾损伤(AKI,3期,KDIGO),伴有肾病综合征、进行性少尿、呼吸困难伴轻度咳血、小腿水肿和血压升高。血清学结果除极低滴度的抗蛋白酶3抗体外均为阴性。胸部X线片显示弥漫性肺部浸润。肾活检显示坏死性新月体肾小球肾炎,免疫荧光染色显示免疫球蛋白G沿整个GBM呈线性模式。根据整个临床情况,对Goodpaste综合征进行了诊断,并提供了强化治疗,包括血浆置换、环磷酰胺和泼尼松,以及血液透析。患者的总体状况得到了改善。尽管利尿功能已经恢复,但停止血液透析的尝试没有成功。该病例证明了AKI患者诊断警惕的重要性。尽管有支持性,但在许多情况下,血清学检测可能是阴性或不明确的,不应阻止包括肾活检在内的深刻诊断过程。尽管进行了适当的治疗,但抗GBM疾病过程中的晚期诊断与较差的肾脏预后相关。世界肾脏泌尿学杂志。2017年;6(1-2):10-13 doi:https://doi.org/10.14740/wjnu301w
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