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AL amyloidosis: advances in diagnosis and management

Light chain (AL) amyloidosis is a disease in which malignant plasma cell clones affect multiple organs including the heart and kidney. The mechanism for organ function deterioration in AL amyloidosis differs from multiple myeloma. Thus, not all agents used to treat multiple myeloma shows similar eff...

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Autor principal: Koh, Youngil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386888/
https://www.ncbi.nlm.nih.gov/pubmed/32719177
http://dx.doi.org/10.5045/br.2020.S009
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author Koh, Youngil
author_facet Koh, Youngil
author_sort Koh, Youngil
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description Light chain (AL) amyloidosis is a disease in which malignant plasma cell clones affect multiple organs including the heart and kidney. The mechanism for organ function deterioration in AL amyloidosis differs from multiple myeloma. Thus, not all agents used to treat multiple myeloma shows similar efficacy in AL amyloidosis. In AL amyloidosis, both hematologic and organ responses after treatment are important to improve the clinical outcome. Especially, improving heart function is one of the key aspects in the treatment of AL amyloidosis. With recent advances in the understanding of the pathophysiologic mechanism of AL amyloidosis, novel treatment methods are under active trial. In this article, I have reviewed the advances in pathophysiology, diagnosis, risk stratification, and treatment of AL amyloidosis.
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spelling pubmed-73868882020-07-30 AL amyloidosis: advances in diagnosis and management Koh, Youngil Blood Res Review Article Light chain (AL) amyloidosis is a disease in which malignant plasma cell clones affect multiple organs including the heart and kidney. The mechanism for organ function deterioration in AL amyloidosis differs from multiple myeloma. Thus, not all agents used to treat multiple myeloma shows similar efficacy in AL amyloidosis. In AL amyloidosis, both hematologic and organ responses after treatment are important to improve the clinical outcome. Especially, improving heart function is one of the key aspects in the treatment of AL amyloidosis. With recent advances in the understanding of the pathophysiologic mechanism of AL amyloidosis, novel treatment methods are under active trial. In this article, I have reviewed the advances in pathophysiology, diagnosis, risk stratification, and treatment of AL amyloidosis. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2020-07-30 2019-07-30 /pmc/articles/PMC7386888/ /pubmed/32719177 http://dx.doi.org/10.5045/br.2020.S009 Text en © 2020 Korean Society of Hematology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Koh, Youngil
AL amyloidosis: advances in diagnosis and management
title AL amyloidosis: advances in diagnosis and management
title_full AL amyloidosis: advances in diagnosis and management
title_fullStr AL amyloidosis: advances in diagnosis and management
title_full_unstemmed AL amyloidosis: advances in diagnosis and management
title_short AL amyloidosis: advances in diagnosis and management
title_sort al amyloidosis: advances in diagnosis and management
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386888/
https://www.ncbi.nlm.nih.gov/pubmed/32719177
http://dx.doi.org/10.5045/br.2020.S009
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