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Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm
INTRODUCTION: Retroperitoneal tumors account for 0.2% of all neoplasms. Among these tumors, retroperitoneal vascular malformations are particularly rare, with most previously reported cases being venous malformations. CASE PRESENTATION: A 72‐year‐old woman was diagnosed with a retroperitoneal tumor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622200/ https://www.ncbi.nlm.nih.gov/pubmed/37928304 http://dx.doi.org/10.1002/iju5.12632 |
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author | Yanagida, Kazuki Kaneko, Tomoyuki Saito, Koji Yamamoto, Masayoshi Yamamoto, Asako Yamada, Yukio Nakagawa, Tohru |
author_facet | Yanagida, Kazuki Kaneko, Tomoyuki Saito, Koji Yamamoto, Masayoshi Yamamoto, Asako Yamada, Yukio Nakagawa, Tohru |
author_sort | Yanagida, Kazuki |
collection | PubMed |
description | INTRODUCTION: Retroperitoneal tumors account for 0.2% of all neoplasms. Among these tumors, retroperitoneal vascular malformations are particularly rare, with most previously reported cases being venous malformations. CASE PRESENTATION: A 72‐year‐old woman was diagnosed with a retroperitoneal tumor on abdominal computed tomography. The 27‐mm diameter tumor was located away from the right kidney and major vessels in the right perirenal adipose tissue. Contrast‐enhanced computed tomography revealed a heterogeneously enhanced tumor with well‐defined borders. Dynamic contrast‐enhanced magnetic resonance imaging revealed rapid enhancement in the arterial phase and a progressive filling‐in pattern in the delayed phase. Although vascular malformation was suspected, a definitive diagnosis could not be established. The retroperitoneal tumor was excised laparoscopically for therapeutic and diagnostic purposes, and the histopathological diagnosis confirmed it as a capillary arteriovenous malformation. CONCLUSION: Herein, we presented a rare case of retroperitoneal capillary arteriovenous malformation that was difficult to definitively diagnose preoperatively. |
format | Online Article Text |
id | pubmed-10622200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106222002023-11-03 Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm Yanagida, Kazuki Kaneko, Tomoyuki Saito, Koji Yamamoto, Masayoshi Yamamoto, Asako Yamada, Yukio Nakagawa, Tohru IJU Case Rep Case Reports INTRODUCTION: Retroperitoneal tumors account for 0.2% of all neoplasms. Among these tumors, retroperitoneal vascular malformations are particularly rare, with most previously reported cases being venous malformations. CASE PRESENTATION: A 72‐year‐old woman was diagnosed with a retroperitoneal tumor on abdominal computed tomography. The 27‐mm diameter tumor was located away from the right kidney and major vessels in the right perirenal adipose tissue. Contrast‐enhanced computed tomography revealed a heterogeneously enhanced tumor with well‐defined borders. Dynamic contrast‐enhanced magnetic resonance imaging revealed rapid enhancement in the arterial phase and a progressive filling‐in pattern in the delayed phase. Although vascular malformation was suspected, a definitive diagnosis could not be established. The retroperitoneal tumor was excised laparoscopically for therapeutic and diagnostic purposes, and the histopathological diagnosis confirmed it as a capillary arteriovenous malformation. CONCLUSION: Herein, we presented a rare case of retroperitoneal capillary arteriovenous malformation that was difficult to definitively diagnose preoperatively. John Wiley and Sons Inc. 2023-08-28 /pmc/articles/PMC10622200/ /pubmed/37928304 http://dx.doi.org/10.1002/iju5.12632 Text en © 2023 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Yanagida, Kazuki Kaneko, Tomoyuki Saito, Koji Yamamoto, Masayoshi Yamamoto, Asako Yamada, Yukio Nakagawa, Tohru Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title | Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title_full | Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title_fullStr | Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title_full_unstemmed | Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title_short | Retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
title_sort | retroperitoneal capillary arteriovenous malformation mimicking a malignant neoplasm |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622200/ https://www.ncbi.nlm.nih.gov/pubmed/37928304 http://dx.doi.org/10.1002/iju5.12632 |
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