{"title":"复合组织管化分阶段修复Effmann IIA2Y型尿道重复1例","authors":"P.R. Saju, H. Balabhaskar, Sunil Ashok, S.J. Aquil Faris, Maradana Prudhvi Vasanth, Sharoo Shaneej, Jinesh Jayadevan","doi":"10.1016/j.eucr.2025.103137","DOIUrl":null,"url":null,"abstract":"<div><div>Effmann type IIA2Y urethral duplication is a rare congenital anomaly requiring individualized surgical management. We report a pediatric case managed with initial buccal mucosa grafting and perineal urethrostomy, followed by a 9-year loss to follow-up. On return, the graft remained viable, and definitive repair was performed using composite tissue tubularization with buccal mucosa, perineal, and scrotal skin. The patient achieved continent, complication-free voiding. This case highlights the durability of multi-tissue grafts and demonstrates the feasibility of delayed reconstruction in complex urethral anomalies.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103137"},"PeriodicalIF":0.4000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Staged repair of Effmann type IIA2Y urethral duplication using composite tissue tubularization: A case report\",\"authors\":\"P.R. Saju, H. Balabhaskar, Sunil Ashok, S.J. Aquil Faris, Maradana Prudhvi Vasanth, Sharoo Shaneej, Jinesh Jayadevan\",\"doi\":\"10.1016/j.eucr.2025.103137\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Effmann type IIA2Y urethral duplication is a rare congenital anomaly requiring individualized surgical management. We report a pediatric case managed with initial buccal mucosa grafting and perineal urethrostomy, followed by a 9-year loss to follow-up. On return, the graft remained viable, and definitive repair was performed using composite tissue tubularization with buccal mucosa, perineal, and scrotal skin. The patient achieved continent, complication-free voiding. This case highlights the durability of multi-tissue grafts and demonstrates the feasibility of delayed reconstruction in complex urethral anomalies.</div></div>\",\"PeriodicalId\":38188,\"journal\":{\"name\":\"Urology Case Reports\",\"volume\":\"62 \",\"pages\":\"Article 103137\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2025-07-21\",\"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/S2214442025002086\",\"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/S2214442025002086","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Staged repair of Effmann type IIA2Y urethral duplication using composite tissue tubularization: A case report
Effmann type IIA2Y urethral duplication is a rare congenital anomaly requiring individualized surgical management. We report a pediatric case managed with initial buccal mucosa grafting and perineal urethrostomy, followed by a 9-year loss to follow-up. On return, the graft remained viable, and definitive repair was performed using composite tissue tubularization with buccal mucosa, perineal, and scrotal skin. The patient achieved continent, complication-free voiding. This case highlights the durability of multi-tissue grafts and demonstrates the feasibility of delayed reconstruction in complex urethral anomalies.