Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Guoliang, Fontaine, Guy H., Fan, Shuanliang, Yan, Yang, Bode, Peter K., Duru, Firat, Frank, Robert, Saguner, Ardan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Via Medica 2020
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
_version_ 1783685954735702016
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
work_keys_str_mv AT liguoliang rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT fontaineguyh rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT fanshuanliang rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT yanyang rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT bodepeterk rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT durufirat rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT frankrobert rightatrialpathologyinarrhythmogenicrightventriculardysplasia
AT sagunerardanm rightatrialpathologyinarrhythmogenicrightventriculardysplasia