{"title":"后肾腺纤维瘤伪装成威尔姆斯瘤","authors":"Prince Raj, A. Khanolkar, Y. Sarin","doi":"10.21699/ajcr.v7i5.463","DOIUrl":null,"url":null,"abstract":"Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms’ tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms’ tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metanephric adenofibroma. No postoperative chemotherapy was given","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"7 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Metanephric Adenofibroma Masquerading as Wilms’ Tumor\",\"authors\":\"Prince Raj, A. Khanolkar, Y. Sarin\",\"doi\":\"10.21699/ajcr.v7i5.463\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms’ tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms’ tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metanephric adenofibroma. No postoperative chemotherapy was given\",\"PeriodicalId\":89657,\"journal\":{\"name\":\"APSP journal of case reports\",\"volume\":\"7 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"APSP journal of case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21699/ajcr.v7i5.463\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"APSP journal of case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21699/ajcr.v7i5.463","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Metanephric Adenofibroma Masquerading as Wilms’ Tumor
Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms’ tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms’ tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metanephric adenofibroma. No postoperative chemotherapy was given