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Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis

Light-chain (AL) amyloidosis is the most common type of amyloidosis; cardiac involvement is rare but has a poor prognosis. Biventricular hypertrophic cardiomyopathy is an exceptional finding in amyloidosis and its association with obstructive right ventricular gradient is even rarer. We report the c...

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Autores principales: Sanoussi, Hamza, Kourireche, Najla, Oukerraj, Latifa, Cherti, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346850/
https://www.ncbi.nlm.nih.gov/pubmed/30755971
http://dx.doi.org/10.12890/2017_000733
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author Sanoussi, Hamza
Kourireche, Najla
Oukerraj, Latifa
Cherti, Mohammed
author_facet Sanoussi, Hamza
Kourireche, Najla
Oukerraj, Latifa
Cherti, Mohammed
author_sort Sanoussi, Hamza
collection PubMed
description Light-chain (AL) amyloidosis is the most common type of amyloidosis; cardiac involvement is rare but has a poor prognosis. Biventricular hypertrophic cardiomyopathy is an exceptional finding in amyloidosis and its association with obstructive right ventricular gradient is even rarer. We report the case of a male patient with biventricular hypertrophy suggesting amyloidosis, with an obstructive gradient in the right ventricle. LEARNING POINTS: Consider amyloidosis in a patient presenting with signs of congestive heart failure and low or microvoltage on ECG. It is important to examine right ventricle myocardium thickness, as hypertrophy not only occurs in the left ventricle, and look for a right ventricle outflow tract gradient. Analysis of speckle tracking of the myocardium will show deterioration of the basal and medium segments with normal apical segment motion.
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spelling pubmed-63468502019-02-12 Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis Sanoussi, Hamza Kourireche, Najla Oukerraj, Latifa Cherti, Mohammed Eur J Case Rep Intern Med Articles Light-chain (AL) amyloidosis is the most common type of amyloidosis; cardiac involvement is rare but has a poor prognosis. Biventricular hypertrophic cardiomyopathy is an exceptional finding in amyloidosis and its association with obstructive right ventricular gradient is even rarer. We report the case of a male patient with biventricular hypertrophy suggesting amyloidosis, with an obstructive gradient in the right ventricle. LEARNING POINTS: Consider amyloidosis in a patient presenting with signs of congestive heart failure and low or microvoltage on ECG. It is important to examine right ventricle myocardium thickness, as hypertrophy not only occurs in the left ventricle, and look for a right ventricle outflow tract gradient. Analysis of speckle tracking of the myocardium will show deterioration of the basal and medium segments with normal apical segment motion. SMC Media Srl 2017-10-02 /pmc/articles/PMC6346850/ /pubmed/30755971 http://dx.doi.org/10.12890/2017_000733 Text en © EFIM 2017 This article is licensed under a Commons Attribution Non-Commercial 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Articles
Sanoussi, Hamza
Kourireche, Najla
Oukerraj, Latifa
Cherti, Mohammed
Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title_full Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title_fullStr Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title_full_unstemmed Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title_short Right Ventricle Outflow Obstruction in Biventricular Hypertrophic Cardiomyopathy in Amyloidosis
title_sort right ventricle outflow obstruction in biventricular hypertrophic cardiomyopathy in amyloidosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346850/
https://www.ncbi.nlm.nih.gov/pubmed/30755971
http://dx.doi.org/10.12890/2017_000733
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