{"title":"A rare giant renal angiomyolipoma in a 17-year-old male: A case report","authors":"Fred Laizer , Hanson Nkini , Heri Babu , Erasto Medard , Amon Bamanyis , Teodros Veronesi","doi":"10.1016/j.eucr.2024.102887","DOIUrl":null,"url":null,"abstract":"<div><div>Renal angiomyolipoma is an uncommon benign tumor that mostly affects adults and is highly associated with tuberous sclerosis. It's very uncommon for it to affect adolescents. In this case, a 17-year-old male with abdominal pain and distension was diagnosed with sporadic giant renal angiomyolipoma. Histopathology confirmed the diagnosis after a successful nephrectomy. Though rare in teenagers, giant renal angiomyolipoma can be managed with surgery. Histopathology is a mainstay of confirming the diagnosis.</div></div><div><h3>Conclusion</h3><div>This case highlights the difficulties in managing big retroperitoneal tumors in teenagers and the necessity of taking sporadic angiomyolipoma into account when making a differential diagnosis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102887"},"PeriodicalIF":0.5000,"publicationDate":"2024-11-22","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/S2214442024002419","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
Renal angiomyolipoma is an uncommon benign tumor that mostly affects adults and is highly associated with tuberous sclerosis. It's very uncommon for it to affect adolescents. In this case, a 17-year-old male with abdominal pain and distension was diagnosed with sporadic giant renal angiomyolipoma. Histopathology confirmed the diagnosis after a successful nephrectomy. Though rare in teenagers, giant renal angiomyolipoma can be managed with surgery. Histopathology is a mainstay of confirming the diagnosis.
Conclusion
This case highlights the difficulties in managing big retroperitoneal tumors in teenagers and the necessity of taking sporadic angiomyolipoma into account when making a differential diagnosis.