Renandha Septaryan Yustira , Sean Peter Haruman , Renaningtyas Tambun , Gerhard Reinaldi Situmorang
{"title":"囊性肾母细胞瘤,囊性部分分化肾母细胞瘤,还是囊性肾瘤?病例报告及文献回顾","authors":"Renandha Septaryan Yustira , Sean Peter Haruman , Renaningtyas Tambun , Gerhard Reinaldi Situmorang","doi":"10.1016/j.eucr.2025.103186","DOIUrl":null,"url":null,"abstract":"<div><div>Wilms tumor, typically a solid pediatric kidney cancer, can rarely appear cystic, mimicking cystic nephroma or cystic partially differentiated nephroblastoma. We report a 20-month-old boy presented with a right abdominal mass, hypertension, and poor appetite. MRI showed a cystic renal tumor, requiring primary nephrectomy without chemotherapy. Postoperative histology revealed a cystic Wilms tumor, necessitating further treatment. This case highlights the diagnostic challenge of cystic renal tumors and emphasizes the importance of histopathology in guiding management. Surgical and chemotherapeutic strategies must be carefully individualized based on clinical and imaging findings.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"63 ","pages":"Article 103186"},"PeriodicalIF":0.4000,"publicationDate":"2025-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cystic wilms tumor, cystic partially differentiated nephroblastoma, or cystic nephroma? A case report and review of the literature\",\"authors\":\"Renandha Septaryan Yustira , Sean Peter Haruman , Renaningtyas Tambun , Gerhard Reinaldi Situmorang\",\"doi\":\"10.1016/j.eucr.2025.103186\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Wilms tumor, typically a solid pediatric kidney cancer, can rarely appear cystic, mimicking cystic nephroma or cystic partially differentiated nephroblastoma. We report a 20-month-old boy presented with a right abdominal mass, hypertension, and poor appetite. MRI showed a cystic renal tumor, requiring primary nephrectomy without chemotherapy. Postoperative histology revealed a cystic Wilms tumor, necessitating further treatment. This case highlights the diagnostic challenge of cystic renal tumors and emphasizes the importance of histopathology in guiding management. Surgical and chemotherapeutic strategies must be carefully individualized based on clinical and imaging findings.</div></div>\",\"PeriodicalId\":38188,\"journal\":{\"name\":\"Urology Case Reports\",\"volume\":\"63 \",\"pages\":\"Article 103186\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2025-08-31\",\"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/S2214442025002578\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214442025002578","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Cystic wilms tumor, cystic partially differentiated nephroblastoma, or cystic nephroma? A case report and review of the literature
Wilms tumor, typically a solid pediatric kidney cancer, can rarely appear cystic, mimicking cystic nephroma or cystic partially differentiated nephroblastoma. We report a 20-month-old boy presented with a right abdominal mass, hypertension, and poor appetite. MRI showed a cystic renal tumor, requiring primary nephrectomy without chemotherapy. Postoperative histology revealed a cystic Wilms tumor, necessitating further treatment. This case highlights the diagnostic challenge of cystic renal tumors and emphasizes the importance of histopathology in guiding management. Surgical and chemotherapeutic strategies must be carefully individualized based on clinical and imaging findings.