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Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child

Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypoxemia. Generally, PAVMs were congenital, most commo...

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Autores principales: Ali Mohamed, Daoud, Waiss, Amarkak, Onka, Behyamet, Mohamed, Walid, Allali, Nazik, Chat, Latifa, El Haddad, Siham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641107/
https://www.ncbi.nlm.nih.gov/pubmed/34869794
http://dx.doi.org/10.1177/2333794X211051186
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author Ali Mohamed, Daoud
Waiss, Amarkak
Onka, Behyamet
Mohamed, Walid
Allali, Nazik
Chat, Latifa
El Haddad, Siham
author_facet Ali Mohamed, Daoud
Waiss, Amarkak
Onka, Behyamet
Mohamed, Walid
Allali, Nazik
Chat, Latifa
El Haddad, Siham
author_sort Ali Mohamed, Daoud
collection PubMed
description Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypoxemia. Generally, PAVMs were congenital, most commonly associated with (Hereditary hemorrhagic teleangiectasia (HHT). The age of diagnosis is very variable, range neonatal to adulthood, mostly diagnosed in the first 3 decades of life and clinical manifestations occur later in life generally. Here, we report PAVMs discovered incidentally in a 10-years-old child without any known risk factor.
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spelling pubmed-86411072021-12-04 Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child Ali Mohamed, Daoud Waiss, Amarkak Onka, Behyamet Mohamed, Walid Allali, Nazik Chat, Latifa El Haddad, Siham Glob Pediatr Health Case Report Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypoxemia. Generally, PAVMs were congenital, most commonly associated with (Hereditary hemorrhagic teleangiectasia (HHT). The age of diagnosis is very variable, range neonatal to adulthood, mostly diagnosed in the first 3 decades of life and clinical manifestations occur later in life generally. Here, we report PAVMs discovered incidentally in a 10-years-old child without any known risk factor. SAGE Publications 2021-11-30 /pmc/articles/PMC8641107/ /pubmed/34869794 http://dx.doi.org/10.1177/2333794X211051186 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Ali Mohamed, Daoud
Waiss, Amarkak
Onka, Behyamet
Mohamed, Walid
Allali, Nazik
Chat, Latifa
El Haddad, Siham
Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title_full Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title_fullStr Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title_full_unstemmed Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title_short Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child
title_sort pulmonary arteriovenous malformations incidentalloma in a 10-years-old child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641107/
https://www.ncbi.nlm.nih.gov/pubmed/34869794
http://dx.doi.org/10.1177/2333794X211051186
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