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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-8842016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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