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尼达尼布治疗特发性肺纤维化后发生的抗肾小球基底膜肾小球肾炎:一例报告

Anti-glomerular basement membrane glomerulonephritis following nintedanib for idiopathic pulmonary fibrosis: a case report.

作者信息

Ismail Ibrahim, Nigam Sonu, Parnham Alan, Srinivasa Vinay

机构信息

Gold Coast University Hospital, Southport, QLD, Australia.

Gold Coast University Hospital, Department of Pathology, Griffith University School of Medicine, Southport, QLD, Australia.

出版信息

J Med Case Rep. 2017 Aug 6;11(1):214. doi: 10.1186/s13256-017-1384-2.

Abstract

BACKGROUND

We report a previously unrecognized and unreported case of a patient with anti-glomerular basement membrane glomerulonephritis following nintedanib, an orally active small molecule tyrosine kinase inhibitor.

CASE PRESENTATION

A 59-year-old Caucasian woman with a history of idiopathic pulmonary fibrosis presented with severe acute kidney injury (creatinine 285 umol/L) secondary to anti-glomerular basement membrane glomerulonephritis disease 4 months after commencement of nintedanib. She had hematuria with red blood cell casts, nephrotic range proteinuria (3.5g/24 hours) and significantly elevated anti-glomerular basement membrane glomerulonephritis titers at 860 chemiluminescent units. A kidney biopsy confirmed severe crescentic glomerulonephritis with linear immunoglobulin G deposition in glomerular basement membrane. Despite the commencement of treatment with plasma exchange and cyclophosphamide, she remained dialysis dependent. Nintedanib was discontinued.

CONCLUSIONS

Onset of acute anti-glomerular basement membrane glomerulonephritis was found to be associated with recent nintedanib use suggesting that nintedanib may be a potential trigger for anti-glomerular basement membrane glomerulonephritis. This case highlights the importance of close monitoring of patients receiving new targeted therapies. Management of novel targeted agents in patients receiving dialysis is challenging because of the scarcity of specific data.

摘要

背景

我们报告了一例先前未被认识和报道的病例,一名患者在服用口服活性小分子酪氨酸激酶抑制剂尼达尼布后发生抗肾小球基底膜肾小球肾炎。

病例介绍

一名59岁的白种女性,有特发性肺纤维化病史,在开始服用尼达尼布4个月后,因抗肾小球基底膜肾小球肾炎出现严重急性肾损伤(肌酐285 μmol/L)。她有血尿伴红细胞管型、肾病范围蛋白尿(3.5g/24小时),抗肾小球基底膜肾小球肾炎滴度显著升高,达860化学发光单位。肾活检证实为严重新月体性肾小球肾炎,免疫球蛋白G在肾小球基底膜呈线性沉积。尽管开始进行血浆置换和环磷酰胺治疗,但她仍依赖透析。尼达尼布停药。

结论

发现急性抗肾小球基底膜肾小球肾炎的发病与近期使用尼达尼布有关,提示尼达尼布可能是抗肾小球基底膜肾小球肾炎的潜在触发因素。该病例强调了密切监测接受新靶向治疗患者的重要性。由于缺乏具体数据,对接受透析的患者管理新型靶向药物具有挑战性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9044/5545090/6ac61cdf0363/13256_2017_1384_Fig1_HTML.jpg

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