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Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study

A 4 month-old, 14.8 kg, male Newfoundland dog was presented for cardiovascular evaluation following detection of a heart murmur. Echocardiography revealed enlargement of the sinuses of Valsalva and marked, diffuse dilation of the ascending aorta (annuloaortic ectasia, AAE), with mild/equivocal subao...

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Autores principales: Côté, Etienne, Zhang, Rong-Mo, Kaiser, Nicole, Reinhardt, Dieter P., Martin, Chelsea K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526017/
https://www.ncbi.nlm.nih.gov/pubmed/34607531
http://dx.doi.org/10.1080/01652176.2021.1961039
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author Côté, Etienne
Zhang, Rong-Mo
Kaiser, Nicole
Reinhardt, Dieter P.
Martin, Chelsea K.
author_facet Côté, Etienne
Zhang, Rong-Mo
Kaiser, Nicole
Reinhardt, Dieter P.
Martin, Chelsea K.
author_sort Côté, Etienne
collection PubMed
description A 4 month-old, 14.8 kg, male Newfoundland dog was presented for cardiovascular evaluation following detection of a heart murmur. Echocardiography revealed enlargement of the sinuses of Valsalva and marked, diffuse dilation of the ascending aorta (annuloaortic ectasia, AAE), with mild/equivocal subaortic stenosis (SAS). The dog was monitored over the duration of its lifetime, with serial echocardiograms performed at 5, 6, and 8 months and 1, 2, 3, 4, 8, and 10 years demonstrating persistent, diffuse dilation of the ascending aorta. The dog lived until it was 10 years old and died of metastatic carcinoma. Postmortem examination confirmed AAE and mild SAS. Hematoxylin and eosin and Weigert van Gieson stains were used to compare the ascending aorta to the descending aorta and left subclavian artery, and to compare aortic samples to those of three control dogs. Histopathologic evaluation revealed mild medial degeneration in the ascending aorta of all four dogs. Immunofluorescent microscopy was used for determining the deposition of proteins known to play a role in aortic aneurysms in humans: fibrillin-1 (FBN1), latent transforming growth factor beta binding protein 4 (LTBP4) and fibronectin. The ascending aorta of the AAE case demonstrated reduced deposition of FBN1, indicating that its loss may have contributed to aortic dilation. Diffuse, primary ascending aortic dilation is uncommonly reported in dogs; when it is, it carries a poor prognosis. This case provides an important example of marked dilation of the ascending aorta in a dog that lived with no associated adverse effects for 10 years.
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spelling pubmed-85260172021-10-20 Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study Côté, Etienne Zhang, Rong-Mo Kaiser, Nicole Reinhardt, Dieter P. Martin, Chelsea K. Vet Q Case Report A 4 month-old, 14.8 kg, male Newfoundland dog was presented for cardiovascular evaluation following detection of a heart murmur. Echocardiography revealed enlargement of the sinuses of Valsalva and marked, diffuse dilation of the ascending aorta (annuloaortic ectasia, AAE), with mild/equivocal subaortic stenosis (SAS). The dog was monitored over the duration of its lifetime, with serial echocardiograms performed at 5, 6, and 8 months and 1, 2, 3, 4, 8, and 10 years demonstrating persistent, diffuse dilation of the ascending aorta. The dog lived until it was 10 years old and died of metastatic carcinoma. Postmortem examination confirmed AAE and mild SAS. Hematoxylin and eosin and Weigert van Gieson stains were used to compare the ascending aorta to the descending aorta and left subclavian artery, and to compare aortic samples to those of three control dogs. Histopathologic evaluation revealed mild medial degeneration in the ascending aorta of all four dogs. Immunofluorescent microscopy was used for determining the deposition of proteins known to play a role in aortic aneurysms in humans: fibrillin-1 (FBN1), latent transforming growth factor beta binding protein 4 (LTBP4) and fibronectin. The ascending aorta of the AAE case demonstrated reduced deposition of FBN1, indicating that its loss may have contributed to aortic dilation. Diffuse, primary ascending aortic dilation is uncommonly reported in dogs; when it is, it carries a poor prognosis. This case provides an important example of marked dilation of the ascending aorta in a dog that lived with no associated adverse effects for 10 years. Taylor & Francis 2021-10-05 /pmc/articles/PMC8526017/ /pubmed/34607531 http://dx.doi.org/10.1080/01652176.2021.1961039 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Côté, Etienne
Zhang, Rong-Mo
Kaiser, Nicole
Reinhardt, Dieter P.
Martin, Chelsea K.
Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title_full Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title_fullStr Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title_full_unstemmed Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title_short Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
title_sort annuloaortic ectasia in a four-month-old male newfoundland dog: long-term follow-up and immunofluorescent study
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526017/
https://www.ncbi.nlm.nih.gov/pubmed/34607531
http://dx.doi.org/10.1080/01652176.2021.1961039
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