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Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report
RATIONALE: Alemtuzumab is a monoclonal antibody approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). Many autoimmune-mediated adverse events have been associated with alemtuzumab, including renal-limited anti-glomerular basement membrane (GBM) disease. PRESENTING CONCERN: A 5...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573726/ https://www.ncbi.nlm.nih.gov/pubmed/33117548 http://dx.doi.org/10.1177/2054358120962680 |
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author | Harrigan, Amye M. West, Michael L. Geldenhuys, Laurette Poyah, Penelope |
author_facet | Harrigan, Amye M. West, Michael L. Geldenhuys, Laurette Poyah, Penelope |
author_sort | Harrigan, Amye M. |
collection | PubMed |
description | RATIONALE: Alemtuzumab is a monoclonal antibody approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). Many autoimmune-mediated adverse events have been associated with alemtuzumab, including renal-limited anti-glomerular basement membrane (GBM) disease. PRESENTING CONCERN: A 52-year-old female with RRMS presented with acute kidney injury 39 months after receiving 1 cycle of alemtuzumab. She had a history of alemtuzumab-associated hypothyroidism and thrombocytopenia, urinary tract infections, and chronically abnormal urinalyses. DIAGNOSIS: A diagnosis of renal-limited anti-GBM disease was made based on renal biopsy and positive anti-GBM serology. Alemtuzumab was thought to be the trigger of the anti-GBM disease as there were no other exposures or serologic findings suggesting other causes. INTERVENTIONS: She was treated with corticosteroids, cyclophosphamide, and plasmapheresis. She required hemodialysis for acute renal failure. OUTCOMES: Despite treatment, the patient’s renal function did not recover. She remained dialysis-dependent and anti-GBM antibody titers remained elevated 6 months after presentation. TEACHING POINTS: Anti-GBM disease is a life-altering adverse event that can be associated with alemtuzumab. Our case highlights the limitations of monitoring urinalyses as a trigger for anti-GBM antibody testing in patients who have received alemtuzumab and have baseline abnormal urinalyses; such patients may require further protocolized anti-GBM antibody testing, although the optimal frequency of such antibody screening remains unclear. |
format | Online Article Text |
id | pubmed-7573726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75737262020-10-27 Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report Harrigan, Amye M. West, Michael L. Geldenhuys, Laurette Poyah, Penelope Can J Kidney Health Dis Educational Case Report RATIONALE: Alemtuzumab is a monoclonal antibody approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). Many autoimmune-mediated adverse events have been associated with alemtuzumab, including renal-limited anti-glomerular basement membrane (GBM) disease. PRESENTING CONCERN: A 52-year-old female with RRMS presented with acute kidney injury 39 months after receiving 1 cycle of alemtuzumab. She had a history of alemtuzumab-associated hypothyroidism and thrombocytopenia, urinary tract infections, and chronically abnormal urinalyses. DIAGNOSIS: A diagnosis of renal-limited anti-GBM disease was made based on renal biopsy and positive anti-GBM serology. Alemtuzumab was thought to be the trigger of the anti-GBM disease as there were no other exposures or serologic findings suggesting other causes. INTERVENTIONS: She was treated with corticosteroids, cyclophosphamide, and plasmapheresis. She required hemodialysis for acute renal failure. OUTCOMES: Despite treatment, the patient’s renal function did not recover. She remained dialysis-dependent and anti-GBM antibody titers remained elevated 6 months after presentation. TEACHING POINTS: Anti-GBM disease is a life-altering adverse event that can be associated with alemtuzumab. Our case highlights the limitations of monitoring urinalyses as a trigger for anti-GBM antibody testing in patients who have received alemtuzumab and have baseline abnormal urinalyses; such patients may require further protocolized anti-GBM antibody testing, although the optimal frequency of such antibody screening remains unclear. SAGE Publications 2020-10-15 /pmc/articles/PMC7573726/ /pubmed/33117548 http://dx.doi.org/10.1177/2054358120962680 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Educational Case Report Harrigan, Amye M. West, Michael L. Geldenhuys, Laurette Poyah, Penelope Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title | Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title_full | Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title_fullStr | Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title_full_unstemmed | Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title_short | Renal-Limited Antiglomerular Basement Membrane Disease Related To Alemtuzumab: A Case Report |
title_sort | renal-limited antiglomerular basement membrane disease related to alemtuzumab: a case report |
topic | Educational Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573726/ https://www.ncbi.nlm.nih.gov/pubmed/33117548 http://dx.doi.org/10.1177/2054358120962680 |
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