Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report

Arteriovenous malformation (AVM) is a common form of vascular malformation, an abnormal direct communication between an artery and a vein without passing through the capillaries. AVM may just present as hematuria without plain or other symptoms. The article presents a case of a 52-year-old male with...

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Autores principales: Qiu, Shixiang, Wei, Xin, Hu, Hong, Zhao, Xiaowei, Wen, Xiaoxia, Zhong, Li-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466900/
https://www.ncbi.nlm.nih.gov/pubmed/32865100
http://dx.doi.org/10.1177/1557988320923913
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author Qiu, Shixiang
Wei, Xin
Hu, Hong
Zhao, Xiaowei
Wen, Xiaoxia
Zhong, Li-Ming
author_facet Qiu, Shixiang
Wei, Xin
Hu, Hong
Zhao, Xiaowei
Wen, Xiaoxia
Zhong, Li-Ming
author_sort Qiu, Shixiang
collection PubMed
description Arteriovenous malformation (AVM) is a common form of vascular malformation, an abnormal direct communication between an artery and a vein without passing through the capillaries. AVM may just present as hematuria without plain or other symptoms. The article presents a case of a 52-year-old male with gross hematuria diagnosed as AVM of internal pudendal artery, which was successfully managed with superselective arterial embolization using temporary embolization materials.
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spelling pubmed-74669002020-09-16 Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report Qiu, Shixiang Wei, Xin Hu, Hong Zhao, Xiaowei Wen, Xiaoxia Zhong, Li-Ming Am J Mens Health Case Report Arteriovenous malformation (AVM) is a common form of vascular malformation, an abnormal direct communication between an artery and a vein without passing through the capillaries. AVM may just present as hematuria without plain or other symptoms. The article presents a case of a 52-year-old male with gross hematuria diagnosed as AVM of internal pudendal artery, which was successfully managed with superselective arterial embolization using temporary embolization materials. SAGE Publications 2020-08-31 /pmc/articles/PMC7466900/ /pubmed/32865100 http://dx.doi.org/10.1177/1557988320923913 Text en © The Author(s) 2020 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Qiu, Shixiang
Wei, Xin
Hu, Hong
Zhao, Xiaowei
Wen, Xiaoxia
Zhong, Li-Ming
Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title_full Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title_fullStr Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title_full_unstemmed Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title_short Superselective Arterial Embolization of Arteriovenous Malformation of Internal Pudendal Artery, a Rare Cause of Hematuria: A Case Report
title_sort superselective arterial embolization of arteriovenous malformation of internal pudendal artery, a rare cause of hematuria: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466900/
https://www.ncbi.nlm.nih.gov/pubmed/32865100
http://dx.doi.org/10.1177/1557988320923913
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