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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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Detalles Bibliográficos
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
Descripción
Sumario: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.