Staged repair of Effmann type IIA2Y urethral duplication using composite tissue tubularization: A case report

IF 0.4 Q4 UROLOGY & NEPHROLOGY
P.R. Saju, H. Balabhaskar, Sunil Ashok, S.J. Aquil Faris, Maradana Prudhvi Vasanth, Sharoo Shaneej, Jinesh Jayadevan
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引用次数: 0

Abstract

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.
复合组织管化分阶段修复Effmann IIA2Y型尿道重复1例
Effmann IIA2Y型尿道重复是一种罕见的先天性异常,需要个体化手术治疗。我们报告了一个儿童病例,最初采用颊粘膜移植和会阴尿道造口术,随访9年。返回时,移植物仍然存活,并使用颊粘膜,会阴和阴囊皮肤的复合组织管化进行最终修复。患者实现了无并发症的排尿。本病例强调了多组织移植的耐久性,并证明了在复杂尿道异常中延迟重建的可行性。
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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