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伴有巨尿道的复杂尿道重复畸形病例。

Complex case of urethral duplication with megalourethra.

作者信息

Sindjic Sanja, Perovic Sava V, Djinovic Rados P

机构信息

Department of Neonatology, University Children's Hospital, Tirsova 10, Belgrade 11000 Serbia.

出版信息

Urology. 2009 Oct;74(4):903-5. doi: 10.1016/j.urology.2008.12.040. Epub 2009 Jul 22.

Abstract

Urethral duplication and megalourethra are very rare anomalies and their concomitant presence is extremely rare, with only a few published cases. We present a complex case of complete urethral duplication with dorsal megalourethra that was severely stenotic in its bulbar part and meatus, with the ventral urethra atretic distally and dilated proximally. Both the corpus spongiosum and the cavernosum were missing. He had associated upper urinary tract abnormalities. Urethral patency was restored successfully by meatoplasty, staged buccal mucosa graft urethroplasty, and tailoring of the megalourethra. This report is unique regarding the use of a buccal mucosa graft for urethral reconstruction in patients with associated urethral duplication and megalourethra.

摘要

尿道重复和巨尿道是非常罕见的畸形,它们同时存在极为罕见,仅有少数病例报道。我们报告一例复杂的完全性尿道重复合并背侧巨尿道病例,其球部和尿道口严重狭窄,腹侧尿道远端闭锁而近端扩张。海绵体和阴茎海绵体均缺如。患者还伴有上尿路异常。通过尿道口成形术、分期颊黏膜移植尿道成形术以及巨尿道剪裁术成功恢复了尿道通畅。本报告在使用颊黏膜移植进行合并尿道重复和巨尿道患者的尿道重建方面具有独特性。

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