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Right atrial pathology in arrhythmogenic right ventricular dysplasia
BACKGROUND: Atrial fibrillation (AF) is the most common atrial arrhythmia in arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Considering the histologic changes known in the right ventricular (RV) in ARVD, the aim of the present study was to examine right atrial (RA) pathology in pa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Via Medica
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083043/ https://www.ncbi.nlm.nih.gov/pubmed/30394508 http://dx.doi.org/10.5603/CJ.a2018.0123 |
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author | Li, Guoliang Fontaine, Guy H. Fan, Shuanliang Yan, Yang Bode, Peter K. Duru, Firat Frank, Robert Saguner, Ardan M. |
author_facet | Li, Guoliang Fontaine, Guy H. Fan, Shuanliang Yan, Yang Bode, Peter K. Duru, Firat Frank, Robert Saguner, Ardan M. |
author_sort | Li, Guoliang |
collection | PubMed |
description | BACKGROUND: Atrial fibrillation (AF) is the most common atrial arrhythmia in arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Considering the histologic changes known in the right ventricular (RV) in ARVD, the aim of the present study was to examine right atrial (RA) pathology in patients with ARVD. METHODS: Histology of RA and RV was assessed from autopsy material in 3 patients with ARVD without persistent atrial arrhythmia. RA histology in 3 patients with permanent AF without ARVD and 5 patients without cardiovascular disease was also studied. Staining with hematoxylin phloxine saffron was performed for the ARVD patients to identify fibrosis, and hematoxylin-eosin for identification of lymphocytes. Masson’s trichrome staining was performed for control groups taken from a collection of standard glass slides. RESULTS: In all 3 ARVD cases, RA anomalies were observed that revealed a reduction of cardiomyocytes, the presence of adipocytes, some of them inside the mediomural atrial layer and interstitial fibrosis. In 2 ARVD cases, interstitial fibrosis was also associated with a focus of replacement fibrosis, which was also observed in patients with permanent AF without ARVD. The histologic specimen of the RA and RV from the control group without cardiovascular disease did not display any evidence of fat or fibrosis with a preserved cardiomyocyte architecture. CONCLUSIONS: A similar histopathological substrate, as can be observed in the RV of patients with ARVD can also be seen in the RA of these patients. This may explain the high prevalence of atrial arrhythmias, particularly AF, in patients with ARVD. |
format | Online Article Text |
id | pubmed-8083043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Via Medica |
record_format | MEDLINE/PubMed |
spelling | pubmed-80830432021-05-10 Right atrial pathology in arrhythmogenic right ventricular dysplasia Li, Guoliang Fontaine, Guy H. Fan, Shuanliang Yan, Yang Bode, Peter K. Duru, Firat Frank, Robert Saguner, Ardan M. Cardiol J Clinical Cardiology BACKGROUND: Atrial fibrillation (AF) is the most common atrial arrhythmia in arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Considering the histologic changes known in the right ventricular (RV) in ARVD, the aim of the present study was to examine right atrial (RA) pathology in patients with ARVD. METHODS: Histology of RA and RV was assessed from autopsy material in 3 patients with ARVD without persistent atrial arrhythmia. RA histology in 3 patients with permanent AF without ARVD and 5 patients without cardiovascular disease was also studied. Staining with hematoxylin phloxine saffron was performed for the ARVD patients to identify fibrosis, and hematoxylin-eosin for identification of lymphocytes. Masson’s trichrome staining was performed for control groups taken from a collection of standard glass slides. RESULTS: In all 3 ARVD cases, RA anomalies were observed that revealed a reduction of cardiomyocytes, the presence of adipocytes, some of them inside the mediomural atrial layer and interstitial fibrosis. In 2 ARVD cases, interstitial fibrosis was also associated with a focus of replacement fibrosis, which was also observed in patients with permanent AF without ARVD. The histologic specimen of the RA and RV from the control group without cardiovascular disease did not display any evidence of fat or fibrosis with a preserved cardiomyocyte architecture. CONCLUSIONS: A similar histopathological substrate, as can be observed in the RV of patients with ARVD can also be seen in the RA of these patients. This may explain the high prevalence of atrial arrhythmias, particularly AF, in patients with ARVD. Via Medica 2020-01-22 /pmc/articles/PMC8083043/ /pubmed/30394508 http://dx.doi.org/10.5603/CJ.a2018.0123 Text en Copyright © 2019 Via Medica https://creativecommons.org/licenses/by-nc-nd/4.0/This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially. |
spellingShingle | Clinical Cardiology Li, Guoliang Fontaine, Guy H. Fan, Shuanliang Yan, Yang Bode, Peter K. Duru, Firat Frank, Robert Saguner, Ardan M. Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title | Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title_full | Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title_fullStr | Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title_full_unstemmed | Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title_short | Right atrial pathology in arrhythmogenic right ventricular dysplasia |
title_sort | right atrial pathology in arrhythmogenic right ventricular dysplasia |
topic | Clinical Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083043/ https://www.ncbi.nlm.nih.gov/pubmed/30394508 http://dx.doi.org/10.5603/CJ.a2018.0123 |
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