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Spontaneous innominate artery rupture in a patient with systemic sclerosis

We present the case of a 57-year-old female with systemic sclerosis who presented in extremis to our hospital with an acute onset of right upper chest and neck pain with swelling. She deteriorated rapidly due to haemodynamic compromise from suspected bleeding and suffered a cardiac arrest with prolo...

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Detalles Bibliográficos
Autores principales: Ali, Sabreen, DeVile, Michael, Hughes, Rodney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389566/
https://www.ncbi.nlm.nih.gov/pubmed/35991499
http://dx.doi.org/10.1093/omcr/omac084
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author Ali, Sabreen
DeVile, Michael
Hughes, Rodney
author_facet Ali, Sabreen
DeVile, Michael
Hughes, Rodney
author_sort Ali, Sabreen
collection PubMed
description We present the case of a 57-year-old female with systemic sclerosis who presented in extremis to our hospital with an acute onset of right upper chest and neck pain with swelling. She deteriorated rapidly due to haemodynamic compromise from suspected bleeding and suffered a cardiac arrest with prolonged resuscitation. Emergency thoracotomy demonstrated an acute longitudinal tear of the innominate artery/brachiocephalic trunk at the junction of the subclavian and common carotid arteries. This is the first reported case of spontaneous arterial rupture in a patient with systemic sclerosis, and while direct causation is difficult to prove, her history of previous vascular complications with potential ongoing microvascular damage makes a contributory role likely.
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spelling pubmed-93895662022-08-19 Spontaneous innominate artery rupture in a patient with systemic sclerosis Ali, Sabreen DeVile, Michael Hughes, Rodney Oxf Med Case Reports Case Report We present the case of a 57-year-old female with systemic sclerosis who presented in extremis to our hospital with an acute onset of right upper chest and neck pain with swelling. She deteriorated rapidly due to haemodynamic compromise from suspected bleeding and suffered a cardiac arrest with prolonged resuscitation. Emergency thoracotomy demonstrated an acute longitudinal tear of the innominate artery/brachiocephalic trunk at the junction of the subclavian and common carotid arteries. This is the first reported case of spontaneous arterial rupture in a patient with systemic sclerosis, and while direct causation is difficult to prove, her history of previous vascular complications with potential ongoing microvascular damage makes a contributory role likely. Oxford University Press 2022-08-18 /pmc/articles/PMC9389566/ /pubmed/35991499 http://dx.doi.org/10.1093/omcr/omac084 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Ali, Sabreen
DeVile, Michael
Hughes, Rodney
Spontaneous innominate artery rupture in a patient with systemic sclerosis
title Spontaneous innominate artery rupture in a patient with systemic sclerosis
title_full Spontaneous innominate artery rupture in a patient with systemic sclerosis
title_fullStr Spontaneous innominate artery rupture in a patient with systemic sclerosis
title_full_unstemmed Spontaneous innominate artery rupture in a patient with systemic sclerosis
title_short Spontaneous innominate artery rupture in a patient with systemic sclerosis
title_sort spontaneous innominate artery rupture in a patient with systemic sclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389566/
https://www.ncbi.nlm.nih.gov/pubmed/35991499
http://dx.doi.org/10.1093/omcr/omac084
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