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Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report

Pelvic arteriovenous malformation is a rare vascular abnormality, espescially in male patients, and is difficult to treat because of its nature supplied by multiple arterial feeders. We report a 70-year-old male patient admitted due to symptoms of benign prostatic hyperplasia. Ultrasound was perform...

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Detalles Bibliográficos
Autores principales: Nguyen, Luan D., Tran, Hien M., Le, Huy A., Nguyen, Tai T., Bui, Kinh T., Hoang, Loi M., Nguyen, Tung S., Nguyen, Hai H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427981/
https://www.ncbi.nlm.nih.gov/pubmed/37593360
http://dx.doi.org/10.1016/j.eucr.2023.102519
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author Nguyen, Luan D.
Tran, Hien M.
Le, Huy A.
Nguyen, Tai T.
Bui, Kinh T.
Hoang, Loi M.
Nguyen, Tung S.
Nguyen, Hai H.
author_facet Nguyen, Luan D.
Tran, Hien M.
Le, Huy A.
Nguyen, Tai T.
Bui, Kinh T.
Hoang, Loi M.
Nguyen, Tung S.
Nguyen, Hai H.
author_sort Nguyen, Luan D.
collection PubMed
description Pelvic arteriovenous malformation is a rare vascular abnormality, espescially in male patients, and is difficult to treat because of its nature supplied by multiple arterial feeders. We report a 70-year-old male patient admitted due to symptoms of benign prostatic hyperplasia. Ultrasound was performed initially, and no other abnormalities were found other than an enlarged prostate. CT scan later demonstrated a pelvic arteriovenous malformation adjacent to the prostate, with multiple arterial feeders from the right internal iliac artery. Angiography confirmed the diagnosis, and transaterial embolization was successfully done. The symptoms disappeared several days later, and the patient remained asymptompmatic during follow-up.
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spelling pubmed-104279812023-08-17 Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report Nguyen, Luan D. Tran, Hien M. Le, Huy A. Nguyen, Tai T. Bui, Kinh T. Hoang, Loi M. Nguyen, Tung S. Nguyen, Hai H. Urol Case Rep Functional Urology Pelvic arteriovenous malformation is a rare vascular abnormality, espescially in male patients, and is difficult to treat because of its nature supplied by multiple arterial feeders. We report a 70-year-old male patient admitted due to symptoms of benign prostatic hyperplasia. Ultrasound was performed initially, and no other abnormalities were found other than an enlarged prostate. CT scan later demonstrated a pelvic arteriovenous malformation adjacent to the prostate, with multiple arterial feeders from the right internal iliac artery. Angiography confirmed the diagnosis, and transaterial embolization was successfully done. The symptoms disappeared several days later, and the patient remained asymptompmatic during follow-up. Elsevier 2023-08-02 /pmc/articles/PMC10427981/ /pubmed/37593360 http://dx.doi.org/10.1016/j.eucr.2023.102519 Text en © 2023 The Authors 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 Functional Urology
Nguyen, Luan D.
Tran, Hien M.
Le, Huy A.
Nguyen, Tai T.
Bui, Kinh T.
Hoang, Loi M.
Nguyen, Tung S.
Nguyen, Hai H.
Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title_full Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title_fullStr Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title_full_unstemmed Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title_short Pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: A case report
title_sort pelvic arteriovenous malformation mimicking benign prostatic hyperplasia: a case report
topic Functional Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427981/
https://www.ncbi.nlm.nih.gov/pubmed/37593360
http://dx.doi.org/10.1016/j.eucr.2023.102519
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