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依那西普诱发的抗肾小球基底膜病。

Etanercept-Induced Anti-Glomerular Basement Membrane Disease.

作者信息

Al-Chalabi Saif, Wu Henry H L, Chinnadurai Rajkumar, Ponnusamy Arvind

机构信息

Department of Renal Medicine, Royal Preston Hospital, Lancashire Teaching Hospitals NHS Foundation Trust, Fulwood, United Kingdom.

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.

出版信息

Case Rep Nephrol Dial. 2021 Sep 21;11(3):292-300. doi: 10.1159/000518984. eCollection 2021 Sep-Dec.

DOI:10.1159/000518984
PMID:34722648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8543357/
Abstract

Anti-glomerular basement membrane (anti-GBM) disease is a rare form of small-vessel vasculitis that typically causes rapidly progressive glomerulonephritis with or without alveolar haemorrhage. Previously, there has only been one reported case of tumour necrosis factor-α (TNF-α) antagonist-induced anti-GBM disease. Here, we describe the first reported case of etanercept-induced anti-GBM disease. A 55-year-old Caucasian man was referred to our tertiary specialist renal centre with a history of painless macroscopic haematuria. The patient has been receiving weekly etanercept injections over the past 12 months for psoriatic arthropathy. The serum immunology panel results highlighted a significantly raised anti-GBM titre (370.1 U). Etanercept was stopped, and the patient was empirically commenced on pulsed methylprednisolone, cyclophosphamide, and plasma exchange. A renal biopsy showed crescentic glomerulonephritis. Few days after admission, he tested positive for coronavirus disease 2019 (COVID-19), and a decision was made to withhold cyclophosphamide. There was further decline in renal function with hyperkalaemia for which he received 2 sessions of haemodialysis. He was restarted on cyclophosphamide upon discharge. The patient was switched to rituximab treatment afterwards as he developed leucopenia 2 weeks following the commencement of cyclophosphamide. The serum creatinine level continued to improve and remained dialysis-independent. In conclusion, with the increased use of etanercept and other TNF-α antagonists, the prescribing clinician must be aware of the rare but life-threatening drug-induced vasculitis. We recommend careful monitoring of renal indices with the use of this class of medications.

摘要

抗肾小球基底膜(anti-GBM)病是一种罕见的小血管炎,通常导致快速进展性肾小球肾炎,可伴有或不伴有肺泡出血。此前,仅有一例肿瘤坏死因子-α(TNF-α)拮抗剂诱发抗GBM病的报道。在此,我们描述首例依那西普诱发抗GBM病的报道病例。一名55岁的白人男性因无痛性肉眼血尿病史被转诊至我们的三级专科肾脏中心。该患者在过去12个月中每周接受依那西普注射治疗银屑病关节炎。血清免疫学检查结果显示抗GBM抗体滴度显著升高(370.1 U)。停用依那西普,并经验性地给予患者甲泼尼龙冲击治疗、环磷酰胺及血浆置换。肾活检显示新月体性肾小球肾炎。入院几天后,他新型冠状病毒肺炎(COVID-19)检测呈阳性,因此决定停用环磷酰胺。患者肾功能进一步下降并出现高钾血症,为此接受了2次血液透析治疗。出院后重新开始使用环磷酰胺。患者在开始使用环磷酰胺2周后出现白细胞减少,随后改用利妥昔单抗治疗。血清肌酐水平持续改善,患者不再依赖透析。总之,随着依那西普和其他TNF-α拮抗剂使用的增加,处方医生必须意识到这种罕见但危及生命的药物性血管炎。我们建议在使用这类药物时仔细监测肾脏指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/8543357/3801a59f5243/cnd-0011-0292-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/8543357/bcad0a29c418/cnd-0011-0292-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/8543357/3801a59f5243/cnd-0011-0292-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/8543357/bcad0a29c418/cnd-0011-0292-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/8543357/3801a59f5243/cnd-0011-0292-g02.jpg

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本文引用的文献

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J Am Soc Nephrol. 2020 Sep;31(9):1959-1968. doi: 10.1681/ASN.2020060802. Epub 2020 Jul 17.
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Etanercept-associated Nephropathy.依那西普相关肾病
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Spatial and Temporal Clustering of Anti-Glomerular Basement Membrane Disease.抗肾小球基底膜病的时空聚集性
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