Glüer S, Fuchs J, Mildenberger H
Department of Pediatric Surgery, Medizinische Hochschule Hannover, Germany.
J Pediatr Surg. 1998 Apr;33(4):628-31. doi: 10.1016/s0022-3468(98)90330-x.
Penile agenesis is a rare congenital anomaly in which early gender reassignment is recommended. In the past, multiple operations were carried out to form feminized external genitalia. The authors performed a definite genital reconstruction in a neonate using the posterior sagittal approach. Preoperatively, a magnetic resonance imaging (MRI) scan demonstrated erectile tissue, which was preserved and incorporated into the genital plasty. The operation included bilateral orchiectomy, urethral reconstruction, sigmoid vaginal replacement, and formation of the labia. The authors discuss the controversy around gender assessment. They emphasize the urethral hypotrophy to be a main challenge in this anomaly and conclude that immediate complete reconstruction is possible and should be performed in patients with this delicate condition.
阴茎发育不全是一种罕见的先天性异常,建议早期进行性别重新分配。过去,曾进行多次手术以形成女性化的外生殖器。作者采用后矢状入路对一名新生儿进行了确定性的生殖器重建。术前,磁共振成像(MRI)扫描显示有勃起组织,该组织被保留并纳入生殖器整形手术。手术包括双侧睾丸切除术、尿道重建、乙状结肠阴道置换和阴唇成形术。作者讨论了围绕性别评估的争议。他们强调尿道发育不良是这种异常的主要挑战,并得出结论,立即进行完全重建是可行的,对于患有这种棘手病症的患者应该进行重建手术。