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Disfiguring high-flow cervicofacial arteriovenous malformations

Arteriovenous malformations (AVMs) are congenital vascular anomalies resulting from defects in angiogenesis. Approximately 40% of AVMs go undetected after birth and only experience the delayed clinical onset of symptoms in adulthood. AVMs are rare, representing only 1.5% of all vascular anomalies. T...

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Detalles Bibliográficos
Autores principales: Nabawi, Alaa, Abraham, Nader, Nabawi, Ayman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569479/
https://www.ncbi.nlm.nih.gov/pubmed/33101645
http://dx.doi.org/10.1093/jscr/rjaa435
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author Nabawi, Alaa
Abraham, Nader
Nabawi, Ayman
author_facet Nabawi, Alaa
Abraham, Nader
Nabawi, Ayman
author_sort Nabawi, Alaa
collection PubMed
description Arteriovenous malformations (AVMs) are congenital vascular anomalies resulting from defects in angiogenesis. Approximately 40% of AVMs go undetected after birth and only experience the delayed clinical onset of symptoms in adulthood. AVMs are rare, representing only 1.5% of all vascular anomalies. The most common sites for the aberrant vascular nidus are the oral cavity and maxillofacial region, which represent 50% of the cases. AVMs are the most challenging and life-threatening form of vascular malformation. Exsanguination, thrombus detachment and embolization are the most hazardous operative risks. Small case series revealed a 75% recurrence rate during a 5-year follow-up, which adds another layer of complexity to their management. Large lesions in the head and neck cause deformation to the patient and present a challenge to the surgeon during their excision among vital structures and reconstruction of the 3D complex defects.
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spelling pubmed-75694792020-10-22 Disfiguring high-flow cervicofacial arteriovenous malformations Nabawi, Alaa Abraham, Nader Nabawi, Ayman J Surg Case Rep Case Series Arteriovenous malformations (AVMs) are congenital vascular anomalies resulting from defects in angiogenesis. Approximately 40% of AVMs go undetected after birth and only experience the delayed clinical onset of symptoms in adulthood. AVMs are rare, representing only 1.5% of all vascular anomalies. The most common sites for the aberrant vascular nidus are the oral cavity and maxillofacial region, which represent 50% of the cases. AVMs are the most challenging and life-threatening form of vascular malformation. Exsanguination, thrombus detachment and embolization are the most hazardous operative risks. Small case series revealed a 75% recurrence rate during a 5-year follow-up, which adds another layer of complexity to their management. Large lesions in the head and neck cause deformation to the patient and present a challenge to the surgeon during their excision among vital structures and reconstruction of the 3D complex defects. Oxford University Press 2020-10-19 /pmc/articles/PMC7569479/ /pubmed/33101645 http://dx.doi.org/10.1093/jscr/rjaa435 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2020. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Series
Nabawi, Alaa
Abraham, Nader
Nabawi, Ayman
Disfiguring high-flow cervicofacial arteriovenous malformations
title Disfiguring high-flow cervicofacial arteriovenous malformations
title_full Disfiguring high-flow cervicofacial arteriovenous malformations
title_fullStr Disfiguring high-flow cervicofacial arteriovenous malformations
title_full_unstemmed Disfiguring high-flow cervicofacial arteriovenous malformations
title_short Disfiguring high-flow cervicofacial arteriovenous malformations
title_sort disfiguring high-flow cervicofacial arteriovenous malformations
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569479/
https://www.ncbi.nlm.nih.gov/pubmed/33101645
http://dx.doi.org/10.1093/jscr/rjaa435
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