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Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report
BACKGROUND: Monoclonal immunoglobulin deposition disease (MIDD) is a rare condition accounting for < 1% of histopathological diagnoses made on kidney biopsy(1). The best outcomes are seen in those diagnosed and treated promptly, but delay to diagnosis is common with the largest series reporting a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216388/ https://www.ncbi.nlm.nih.gov/pubmed/32398029 http://dx.doi.org/10.1186/s12882-020-01837-2 |
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author | Turner, Michael Crawford, Anna Winterbottom, Claire Flossmann, Oliver Alchi, Bassam Soares, Maria Bhandary, Umanath |
author_facet | Turner, Michael Crawford, Anna Winterbottom, Claire Flossmann, Oliver Alchi, Bassam Soares, Maria Bhandary, Umanath |
author_sort | Turner, Michael |
collection | PubMed |
description | BACKGROUND: Monoclonal immunoglobulin deposition disease (MIDD) is a rare condition accounting for < 1% of histopathological diagnoses made on kidney biopsy(1). The best outcomes are seen in those diagnosed and treated promptly, but delay to diagnosis is common with the largest series reporting a median time from onset of renal impairment to diagnosis of 12 months(2). Here, we report a case of the heavy chain subset of MIDD presenting with positive anti-glomerular basement membrane (anti-GBM) antibodies obscuring the true diagnosis. CASE PRESENTATION: Here, we present a challenging case presenting with oedema, haematoproteiuria, and new renal impairment. Anti-GBM antibodies were positive and prompted treatment as atypical anti-GBM disease. However, they were ultimately proven to be monoclonal and secondary to myeloma. The final diagnosis facilitated effective myeloma treatment which led to complete remission and independence from renal replacement therapy. CONCLUSIONS: This case reinforces the importance of comprehensive histopathological and haematological assessment in making the correct diagnosis. Here it facilitated effective treatment and recovery of renal function. |
format | Online Article Text |
id | pubmed-7216388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72163882020-05-18 Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report Turner, Michael Crawford, Anna Winterbottom, Claire Flossmann, Oliver Alchi, Bassam Soares, Maria Bhandary, Umanath BMC Nephrol Case Report BACKGROUND: Monoclonal immunoglobulin deposition disease (MIDD) is a rare condition accounting for < 1% of histopathological diagnoses made on kidney biopsy(1). The best outcomes are seen in those diagnosed and treated promptly, but delay to diagnosis is common with the largest series reporting a median time from onset of renal impairment to diagnosis of 12 months(2). Here, we report a case of the heavy chain subset of MIDD presenting with positive anti-glomerular basement membrane (anti-GBM) antibodies obscuring the true diagnosis. CASE PRESENTATION: Here, we present a challenging case presenting with oedema, haematoproteiuria, and new renal impairment. Anti-GBM antibodies were positive and prompted treatment as atypical anti-GBM disease. However, they were ultimately proven to be monoclonal and secondary to myeloma. The final diagnosis facilitated effective myeloma treatment which led to complete remission and independence from renal replacement therapy. CONCLUSIONS: This case reinforces the importance of comprehensive histopathological and haematological assessment in making the correct diagnosis. Here it facilitated effective treatment and recovery of renal function. BioMed Central 2020-05-12 /pmc/articles/PMC7216388/ /pubmed/32398029 http://dx.doi.org/10.1186/s12882-020-01837-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Turner, Michael Crawford, Anna Winterbottom, Claire Flossmann, Oliver Alchi, Bassam Soares, Maria Bhandary, Umanath Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title | Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title_full | Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title_fullStr | Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title_full_unstemmed | Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title_short | Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report |
title_sort | heavy chain deposition disease presenting with raised anti-gbm antibody levels; a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216388/ https://www.ncbi.nlm.nih.gov/pubmed/32398029 http://dx.doi.org/10.1186/s12882-020-01837-2 |
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