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Etanercept-Induced Anti-Glomerular Basement Membrane Disease
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 a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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S. Karger AG
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543357/ https://www.ncbi.nlm.nih.gov/pubmed/34722648 http://dx.doi.org/10.1159/000518984 |
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author | Al-Chalabi, Saif Wu, Henry H.L. Chinnadurai, Rajkumar Ponnusamy, Arvind |
author_facet | Al-Chalabi, Saif Wu, Henry H.L. Chinnadurai, Rajkumar Ponnusamy, Arvind |
author_sort | Al-Chalabi, Saif |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8543357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-85433572021-10-29 Etanercept-Induced Anti-Glomerular Basement Membrane Disease Al-Chalabi, Saif Wu, Henry H.L. Chinnadurai, Rajkumar Ponnusamy, Arvind Case Rep Nephrol Dial Case and Review 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. S. Karger AG 2021-09-21 /pmc/articles/PMC8543357/ /pubmed/34722648 http://dx.doi.org/10.1159/000518984 Text en Copyright © 2021 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case and Review Al-Chalabi, Saif Wu, Henry H.L. Chinnadurai, Rajkumar Ponnusamy, Arvind Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title | Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title_full | Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title_fullStr | Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title_full_unstemmed | Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title_short | Etanercept-Induced Anti-Glomerular Basement Membrane Disease |
title_sort | etanercept-induced anti-glomerular basement membrane disease |
topic | Case and Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543357/ https://www.ncbi.nlm.nih.gov/pubmed/34722648 http://dx.doi.org/10.1159/000518984 |
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