首页> 外文期刊>The Journal of Urology >Bladder exstrophy associated with complete urethral duplication: a rare malformation with excellent prognosis.
【24h】

Bladder exstrophy associated with complete urethral duplication: a rare malformation with excellent prognosis.

机译:与完全尿道复制相关的膀胱外翻:罕见的畸形,预后良好。

获取原文
获取原文并翻译 | 示例
           

摘要

PURPOSE: We report the association of complete urethral duplication and bladder exstrophy in 5 males, and describe the main characteristics to achieve diagnosis. MATERIALS AND METHODS: From 1983 to 2000, 5 males with single bladder exstrophy and complete urethral duplication were seen at 3 institutions. Although bladder exstrophy was obvious at birth, only 1 patient had the preoperative diagnosis of associated urethral duplication. All patients were evaluated with abdominal ultrasound, voiding cystourethrogram after bladder closure and cystoscopy. RESULTS: All patients were totally incontinent, including 4 after primary bladder exstrophy closure. Although it was initially unnoticed by the urologist, most patients had leakage from the tip of the penis during the Valsalva maneuver. In all cases bladder exstrophy was single and deeply situated in the pelvis with excellent elasticity. All patients had a normal sized penis with less severe dorsal chordee and conical shaped glans. The duplicate epispadiac urethra did not have a verumontanum. Only 1 of the 5 patients had the correct diagnosis made before primary closure of bladder exstrophy, while in the other 4 diagnosis of a duplicate ventral urethra was made at the time of epispadias or fistula repair. There were no other associated malformations. In all cases the dorsal epispadiac urethral plate was excised and bladder emptying occurred through the ventral urethra, which at cystoscopy had a normal verumontanum. Postoperatively, all patients became continent and voided with good flow through the ventral urethra and, as opposed to many cases of exstrophy and epispadias, had normal size and excellent cosmesis of the penis. CONCLUSIONS: Complete urethral duplication is a rare variant of the exstrophy-epispadias complex. Patients with this anomaly present with a larger and more deeply situated bladder plate than classical exstrophy and a larger penis. A high index of suspicion is necessary to make a preoperative diagnosis. Excision of the dorsal urethral plate and maintenance of the ventral urethra are the treatment of choice, resulting in a continence and normal voiding.
机译:目的:我们报告了5名男性中完全尿道重复与膀胱萎缩的相关性,并描述了实现诊断的主要特征。材料与方法:从1983年至2000年,在3个机构中发现5例具有单膀胱萎缩和完全尿道重复的男性。尽管出生时膀胱外翻明显,但只有1例患者术前诊断出有相关的尿道重复。所有患者均接受腹部超声检查,膀胱闭合和膀胱镜检查后排空膀胱尿道造影。结果:所有患者均完全失禁,其中4例在原发性膀胱萎缩症闭合后。尽管泌尿科医师最初没有注意到它,但是大多数患者在进行瓦尔萨尔瓦手术时都从阴茎尖端漏出。在所有情况下,膀胱外翻都是单个的,并且位于骨盆深处,具有出色的弹性。所有患者的阴茎大小均正常,背腱膜较轻,圆锥形龟头。重复的尿道上尿道尿道没有verumontanum。 5例患者中只有1例在原发性膀胱外翻闭合之前做出了正确的诊断,而在其他4例中,在尿道上裂或瘘管修复时诊断为腹侧尿道重复。没有其他相关的畸形。在所有情况下,均切除腹膜上尿道后尿道板,并通过腹腔尿道排空膀胱,在膀胱镜检查时尿液正常。术后,所有患者进入大陆,并通过腹侧尿道排空,并有良好的血流,与许多萎缩和尿道上裂的病例相反,它们的大小正常,阴茎美观。结论:完全的尿道复制是外生性上皮-上睑外膜复合体的罕见变体。与常规外翻和阴茎较大相比,这种异常患者的膀胱板位置更大,位置更深。要进行术前诊断,必须高度怀疑。切除背侧尿道板和维持腹侧尿道是治疗的选择,可导致尿失禁和正常排尿。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号