{"title":"Incidental finding of polyorchidism during elective orchidopexy in a child: a case report","authors":"Eiman Yassir Musa Hussain , Khadidja Amedjoudj","doi":"10.1016/j.eucr.2025.103197","DOIUrl":null,"url":null,"abstract":"<div><div>Polyorchidism is a rare congenital anomaly characterized by the presence of more than two testes. It is commonly discovered incidentally during surgical exploration. We report a case of a 7-year-old male with Polyorchidism diagnosed during elective surgery for undescended left testis. An intra-scrotal supernumerary testis was found with a cryptorchidic testis located at the inguinal canal. We opted for Orchidectomy of the intrascrotal atrophic testis, and orchidopexy of the healthy testis. Histopathology confirmed the diagnosis. Postoperative recovery and follow-up were uneventful. This case highlights the importance of polyorchidism management based on anatomical and functional findings intraoperatively.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"63 ","pages":"Article 103197"},"PeriodicalIF":0.4000,"publicationDate":"2025-09-02","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/S2214442025002682","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
Polyorchidism is a rare congenital anomaly characterized by the presence of more than two testes. It is commonly discovered incidentally during surgical exploration. We report a case of a 7-year-old male with Polyorchidism diagnosed during elective surgery for undescended left testis. An intra-scrotal supernumerary testis was found with a cryptorchidic testis located at the inguinal canal. We opted for Orchidectomy of the intrascrotal atrophic testis, and orchidopexy of the healthy testis. Histopathology confirmed the diagnosis. Postoperative recovery and follow-up were uneventful. This case highlights the importance of polyorchidism management based on anatomical and functional findings intraoperatively.