Aidan S. Weitzner , Victoria Maxon , Jordan S. Levine , Catherine Robey , Tanisha Martheswaran , Tijesunimi Oni , Chad B. Crigger
{"title":"交叉睾丸异位融合型1例报告及文献讨论","authors":"Aidan S. Weitzner , Victoria Maxon , Jordan S. Levine , Catherine Robey , Tanisha Martheswaran , Tijesunimi Oni , Chad B. Crigger","doi":"10.1016/j.eucr.2025.103220","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Crossed testicular ectopia (CTE) is a rare genitourinary anomaly in which both testes descend through the same inguinal canal.</div></div><div><h3>Case presentation</h3><div>We describe a 10-month-old boy with proximal penoscrotal hypospadias and nonpalpable right testis. Despite normal ultrasound findings on the left, the right testis was not visualized. Diagnostic laparoscopy revealed a right-to-left crossed fused ectopia through a left inguinal hernia. The fused testes were surgically dissected and bilateral orchiopexy was performed successfully.</div></div><div><h3>Conclusion</h3><div>Fusion variants of CTE are extremely rare. This case provides the first surgical description of infant fused CTE and highlights the importance of laparoscopy in management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"63 ","pages":"Article 103220"},"PeriodicalIF":0.4000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fused variant of crossed testicular ectopia: A case report and discussion of the literature\",\"authors\":\"Aidan S. Weitzner , Victoria Maxon , Jordan S. Levine , Catherine Robey , Tanisha Martheswaran , Tijesunimi Oni , Chad B. Crigger\",\"doi\":\"10.1016/j.eucr.2025.103220\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Crossed testicular ectopia (CTE) is a rare genitourinary anomaly in which both testes descend through the same inguinal canal.</div></div><div><h3>Case presentation</h3><div>We describe a 10-month-old boy with proximal penoscrotal hypospadias and nonpalpable right testis. Despite normal ultrasound findings on the left, the right testis was not visualized. Diagnostic laparoscopy revealed a right-to-left crossed fused ectopia through a left inguinal hernia. The fused testes were surgically dissected and bilateral orchiopexy was performed successfully.</div></div><div><h3>Conclusion</h3><div>Fusion variants of CTE are extremely rare. This case provides the first surgical description of infant fused CTE and highlights the importance of laparoscopy in management.</div></div>\",\"PeriodicalId\":38188,\"journal\":{\"name\":\"Urology Case Reports\",\"volume\":\"63 \",\"pages\":\"Article 103220\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2025-09-24\",\"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/S2214442025002918\",\"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/S2214442025002918","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Fused variant of crossed testicular ectopia: A case report and discussion of the literature
Introduction
Crossed testicular ectopia (CTE) is a rare genitourinary anomaly in which both testes descend through the same inguinal canal.
Case presentation
We describe a 10-month-old boy with proximal penoscrotal hypospadias and nonpalpable right testis. Despite normal ultrasound findings on the left, the right testis was not visualized. Diagnostic laparoscopy revealed a right-to-left crossed fused ectopia through a left inguinal hernia. The fused testes were surgically dissected and bilateral orchiopexy was performed successfully.
Conclusion
Fusion variants of CTE are extremely rare. This case provides the first surgical description of infant fused CTE and highlights the importance of laparoscopy in management.