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Scrotal arteriovenous malformation: Case report

Scrotal arteriovenous malformations (AVM) are extremely rare, making them difficult and complex to diagnose, and a therapeutic challenge; few cases of this type have been reported in the literature. This article reports the case of a male patient, 12 years old, with congenital AVM and background of...

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Autores principales: Guerrero Avendaño, Guadalupe Mercedes Lucía, Enríquez García, Rocío, Saldívar Rodea, Carlos Alberto, Sierra Juárez, Miguel Ángel, Sotelo Cuéllar, José Sebastián
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842016/
https://www.ncbi.nlm.nih.gov/pubmed/35198090
http://dx.doi.org/10.1016/j.radcr.2022.01.055
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author Guerrero Avendaño, Guadalupe Mercedes Lucía
Enríquez García, Rocío
Saldívar Rodea, Carlos Alberto
Sierra Juárez, Miguel Ángel
Sotelo Cuéllar, José Sebastián
author_facet Guerrero Avendaño, Guadalupe Mercedes Lucía
Enríquez García, Rocío
Saldívar Rodea, Carlos Alberto
Sierra Juárez, Miguel Ángel
Sotelo Cuéllar, José Sebastián
author_sort Guerrero Avendaño, Guadalupe Mercedes Lucía
collection PubMed
description Scrotal arteriovenous malformations (AVM) are extremely rare, making them difficult and complex to diagnose, and a therapeutic challenge; few cases of this type have been reported in the literature. This article reports the case of a male patient, 12 years old, with congenital AVM and background of treatment with sclerotherapy and embolization: it was decided to perform a surgical resection, which was successful. Angiography is obligatory in arteriolar cases, and it was backed up with surgical AVM treatment, taking into account the great importance of pre-surgical embolization.
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spelling pubmed-88420162022-02-22 Scrotal arteriovenous malformation: Case report Guerrero Avendaño, Guadalupe Mercedes Lucía Enríquez García, Rocío Saldívar Rodea, Carlos Alberto Sierra Juárez, Miguel Ángel Sotelo Cuéllar, José Sebastián Radiol Case Rep Case Report Scrotal arteriovenous malformations (AVM) are extremely rare, making them difficult and complex to diagnose, and a therapeutic challenge; few cases of this type have been reported in the literature. This article reports the case of a male patient, 12 years old, with congenital AVM and background of treatment with sclerotherapy and embolization: it was decided to perform a surgical resection, which was successful. Angiography is obligatory in arteriolar cases, and it was backed up with surgical AVM treatment, taking into account the great importance of pre-surgical embolization. Elsevier 2022-02-09 /pmc/articles/PMC8842016/ /pubmed/35198090 http://dx.doi.org/10.1016/j.radcr.2022.01.055 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Guerrero Avendaño, Guadalupe Mercedes Lucía
Enríquez García, Rocío
Saldívar Rodea, Carlos Alberto
Sierra Juárez, Miguel Ángel
Sotelo Cuéllar, José Sebastián
Scrotal arteriovenous malformation: Case report
title Scrotal arteriovenous malformation: Case report
title_full Scrotal arteriovenous malformation: Case report
title_fullStr Scrotal arteriovenous malformation: Case report
title_full_unstemmed Scrotal arteriovenous malformation: Case report
title_short Scrotal arteriovenous malformation: Case report
title_sort scrotal arteriovenous malformation: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842016/
https://www.ncbi.nlm.nih.gov/pubmed/35198090
http://dx.doi.org/10.1016/j.radcr.2022.01.055
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