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Severe nephritis as initial sign of Waldenström’s macroglobulinemia

Waldenström’s macroglobulinemia (WM), characterized with monoclonal immunoglobulins of type M and lymphoplasmacytic lymphoma, is a rare clonal Bcell disorder. WM usually present as an indolent lymphoma, and renal involvement is, in contrast to multiple myeloma, very rarely seen. We present a patient...

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Autores principales: Knoop, Thomas, Larsen, Kristin Kampevold, Leh, Friedemann, Hemsing, Anette Lodvir, Teigen, Ingrid Anna, Reikvam, Håkon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945070/
https://www.ncbi.nlm.nih.gov/pubmed/31929868
http://dx.doi.org/10.4081/cp.2019.1184
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author Knoop, Thomas
Larsen, Kristin Kampevold
Leh, Friedemann
Hemsing, Anette Lodvir
Teigen, Ingrid Anna
Reikvam, Håkon
author_facet Knoop, Thomas
Larsen, Kristin Kampevold
Leh, Friedemann
Hemsing, Anette Lodvir
Teigen, Ingrid Anna
Reikvam, Håkon
author_sort Knoop, Thomas
collection PubMed
description Waldenström’s macroglobulinemia (WM), characterized with monoclonal immunoglobulins of type M and lymphoplasmacytic lymphoma, is a rare clonal Bcell disorder. WM usually present as an indolent lymphoma, and renal involvement is, in contrast to multiple myeloma, very rarely seen. We present a patient presenting with severe nephritis and nephrotic range proteinuria of more than 9 g/day as initial manifestations of WM. Furthermore, we discuss diagnostic and therapeutic approaches for this rare manifestation of the disease, in the light of recent research and treatment recommendations.
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spelling pubmed-69450702020-01-10 Severe nephritis as initial sign of Waldenström’s macroglobulinemia Knoop, Thomas Larsen, Kristin Kampevold Leh, Friedemann Hemsing, Anette Lodvir Teigen, Ingrid Anna Reikvam, Håkon Clin Pract Case Report Waldenström’s macroglobulinemia (WM), characterized with monoclonal immunoglobulins of type M and lymphoplasmacytic lymphoma, is a rare clonal Bcell disorder. WM usually present as an indolent lymphoma, and renal involvement is, in contrast to multiple myeloma, very rarely seen. We present a patient presenting with severe nephritis and nephrotic range proteinuria of more than 9 g/day as initial manifestations of WM. Furthermore, we discuss diagnostic and therapeutic approaches for this rare manifestation of the disease, in the light of recent research and treatment recommendations. PAGEPress Publications, Pavia, Italy 2019-12-19 /pmc/articles/PMC6945070/ /pubmed/31929868 http://dx.doi.org/10.4081/cp.2019.1184 Text en ©Copyright: the Author(s), 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Case Report
Knoop, Thomas
Larsen, Kristin Kampevold
Leh, Friedemann
Hemsing, Anette Lodvir
Teigen, Ingrid Anna
Reikvam, Håkon
Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title_full Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title_fullStr Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title_full_unstemmed Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title_short Severe nephritis as initial sign of Waldenström’s macroglobulinemia
title_sort severe nephritis as initial sign of waldenström’s macroglobulinemia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945070/
https://www.ncbi.nlm.nih.gov/pubmed/31929868
http://dx.doi.org/10.4081/cp.2019.1184
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