Alessandro Vengjer , Matheus Miranda Paiva , Eloi Guilherme Provinciali Moccellin , André Segura da Motta , Raphael Oliveira Emerick Constantino , Ana Luiza Tunes Ortiz , Katia Ramos Moreira Leite
{"title":"Solitary fibrous tumor of the prostate: Case report and literature review","authors":"Alessandro Vengjer , Matheus Miranda Paiva , Eloi Guilherme Provinciali Moccellin , André Segura da Motta , Raphael Oliveira Emerick Constantino , Ana Luiza Tunes Ortiz , Katia Ramos Moreira Leite","doi":"10.1016/j.eucr.2025.103207","DOIUrl":null,"url":null,"abstract":"<div><div>Solitary fibrous tumor (SFT) of the prostate is a rare mesenchymal neoplasm with only a few cases reported. Its clinical presentation often mimics benign prostatic hyperplasia, and imaging findings are nonspecific. Diagnosis relies on histopathology and immunohistochemistry, particularly STAT6 nuclear expression. Most cases follow a benign course, but some may exhibit aggressive behavior. Complete surgical resection with clear margins is the treatment of choice, with no established role for adjuvant therapy. This report discusses a case of prostatic SFT, emphasizing its diagnostic challenges, imaging findings, and surgical management, contributing to the limited literature on this rare entity.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"63 ","pages":"Article 103207"},"PeriodicalIF":0.4000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214442025002785","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Solitary fibrous tumor (SFT) of the prostate is a rare mesenchymal neoplasm with only a few cases reported. Its clinical presentation often mimics benign prostatic hyperplasia, and imaging findings are nonspecific. Diagnosis relies on histopathology and immunohistochemistry, particularly STAT6 nuclear expression. Most cases follow a benign course, but some may exhibit aggressive behavior. Complete surgical resection with clear margins is the treatment of choice, with no established role for adjuvant therapy. This report discusses a case of prostatic SFT, emphasizing its diagnostic challenges, imaging findings, and surgical management, contributing to the limited literature on this rare entity.