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Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis

We discuss here an uncommon condition of neurogenic hypotension in the context of immunoglobulin light chain (amyloid light-chain) amyloidosis. The most serious feature was autonomic nervous system impairment, mainly characterized by severe refractory orthostatic hypotension, which became progressiv...

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Detalles Bibliográficos
Autores principales: Pelusi, Serena, Lombardi, Rosa, Airaghi, Lorena, Burdick, Larry, Rango, Mario, Penatti, Alessandra, Fargion, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331769/
https://www.ncbi.nlm.nih.gov/pubmed/28255325
http://dx.doi.org/10.4103/1735-1995.193508
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author Pelusi, Serena
Lombardi, Rosa
Airaghi, Lorena
Burdick, Larry
Rango, Mario
Penatti, Alessandra
Fargion, Silvia
author_facet Pelusi, Serena
Lombardi, Rosa
Airaghi, Lorena
Burdick, Larry
Rango, Mario
Penatti, Alessandra
Fargion, Silvia
author_sort Pelusi, Serena
collection PubMed
description We discuss here an uncommon condition of neurogenic hypotension in the context of immunoglobulin light chain (amyloid light-chain) amyloidosis. The most serious feature was autonomic nervous system impairment, mainly characterized by severe refractory orthostatic hypotension, which became progressively invalidating, forcing the patient to bed. Moreover, since the systemic involvement of the disease, the patient presented also diarrhea, dysphagia, asthenia, peripheral edema because of gastrointestinal, and kidney dysfunction. Eventually, the massive myocardial depression and infiltration led to a fatal outcome.
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spelling pubmed-53317692017-03-02 Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis Pelusi, Serena Lombardi, Rosa Airaghi, Lorena Burdick, Larry Rango, Mario Penatti, Alessandra Fargion, Silvia J Res Med Sci Case Report We discuss here an uncommon condition of neurogenic hypotension in the context of immunoglobulin light chain (amyloid light-chain) amyloidosis. The most serious feature was autonomic nervous system impairment, mainly characterized by severe refractory orthostatic hypotension, which became progressively invalidating, forcing the patient to bed. Moreover, since the systemic involvement of the disease, the patient presented also diarrhea, dysphagia, asthenia, peripheral edema because of gastrointestinal, and kidney dysfunction. Eventually, the massive myocardial depression and infiltration led to a fatal outcome. Medknow Publications & Media Pvt Ltd 2016-11-07 /pmc/articles/PMC5331769/ /pubmed/28255325 http://dx.doi.org/10.4103/1735-1995.193508 Text en Copyright: © 2016 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Pelusi, Serena
Lombardi, Rosa
Airaghi, Lorena
Burdick, Larry
Rango, Mario
Penatti, Alessandra
Fargion, Silvia
Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title_full Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title_fullStr Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title_full_unstemmed Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title_short Progressively invalidating orthostatic hypotension: A common symptom for a challenging diagnosis
title_sort progressively invalidating orthostatic hypotension: a common symptom for a challenging diagnosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331769/
https://www.ncbi.nlm.nih.gov/pubmed/28255325
http://dx.doi.org/10.4103/1735-1995.193508
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