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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...

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Autores principales: Yanagida, Kazuki, Kaneko, Tomoyuki, Saito, Koji, Yamamoto, Masayoshi, Yamamoto, Asako, Yamada, Yukio, Nakagawa, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
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.
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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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