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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...

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Autores principales: Al-Chalabi, Saif, Wu, Henry H.L., Chinnadurai, Rajkumar, Ponnusamy, Arvind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
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.
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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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