A rare systemic etiology of heart failure and liver dysfunction

Systemic amyloidosis is a rare condition that can manifest with cardiomyopathy, hepatic dysfunction, and renal disease. Diagnosis is often missed and/or delayed due to chronic multi‐system involvement and indeterminate signs and symptoms. Treatment generally involves systemic therapy and autologous...

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Detalles Bibliográficos
Autores principales: Lee, Christopher, Chau, Edward, Patel, Sumit, Zhao, Diana, Yang, Alexander H., Lee, Brian T., Alexander, Jacob, Ostrzega, Enrique, Sarte, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637331/
https://www.ncbi.nlm.nih.gov/pubmed/31360486
http://dx.doi.org/10.1002/ccr3.2229
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author Lee, Christopher
Chau, Edward
Patel, Sumit
Zhao, Diana
Yang, Alexander H.
Lee, Brian T.
Alexander, Jacob
Ostrzega, Enrique
Sarte, Patrick
author_facet Lee, Christopher
Chau, Edward
Patel, Sumit
Zhao, Diana
Yang, Alexander H.
Lee, Brian T.
Alexander, Jacob
Ostrzega, Enrique
Sarte, Patrick
author_sort Lee, Christopher
collection PubMed
description Systemic amyloidosis is a rare condition that can manifest with cardiomyopathy, hepatic dysfunction, and renal disease. Diagnosis is often missed and/or delayed due to chronic multi‐system involvement and indeterminate signs and symptoms. Treatment generally involves systemic therapy and autologous stem‐cell transplantation.
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spelling pubmed-66373312019-07-29 A rare systemic etiology of heart failure and liver dysfunction Lee, Christopher Chau, Edward Patel, Sumit Zhao, Diana Yang, Alexander H. Lee, Brian T. Alexander, Jacob Ostrzega, Enrique Sarte, Patrick Clin Case Rep Case Reports Systemic amyloidosis is a rare condition that can manifest with cardiomyopathy, hepatic dysfunction, and renal disease. Diagnosis is often missed and/or delayed due to chronic multi‐system involvement and indeterminate signs and symptoms. Treatment generally involves systemic therapy and autologous stem‐cell transplantation. John Wiley and Sons Inc. 2019-06-03 /pmc/articles/PMC6637331/ /pubmed/31360486 http://dx.doi.org/10.1002/ccr3.2229 Text en © 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Lee, Christopher
Chau, Edward
Patel, Sumit
Zhao, Diana
Yang, Alexander H.
Lee, Brian T.
Alexander, Jacob
Ostrzega, Enrique
Sarte, Patrick
A rare systemic etiology of heart failure and liver dysfunction
title A rare systemic etiology of heart failure and liver dysfunction
title_full A rare systemic etiology of heart failure and liver dysfunction
title_fullStr A rare systemic etiology of heart failure and liver dysfunction
title_full_unstemmed A rare systemic etiology of heart failure and liver dysfunction
title_short A rare systemic etiology of heart failure and liver dysfunction
title_sort rare systemic etiology of heart failure and liver dysfunction
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637331/
https://www.ncbi.nlm.nih.gov/pubmed/31360486
http://dx.doi.org/10.1002/ccr3.2229
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