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完全性输尿管重复畸形合并异位输尿管:保守性手术治疗

Ectopic ureter with complete ureteric duplication: conservative surgical management.

作者信息

el Ghoneimi A, Miranda J, Truong T, Monfort G

机构信息

Department of Pediatric Urology, Hopital d'enfants de la Timone, Marseille, France.

出版信息

J Pediatr Surg. 1996 Apr;31(4):467-72. doi: 10.1016/s0022-3468(96)90476-5.

DOI:10.1016/s0022-3468(96)90476-5
PMID:8801293
Abstract

To assess the outcome of conservative procedures, the authors reviewed their experience in the management of 31 ectopic ureters with complete ureteric duplication. Twenty-eight girls and three boys (aged 19 days to 10 years; mean, 30 months) were operated on between 1968 and 1994. Twenty-four of the children presented for evaluation of dribbling urinary incontinence and/or febrile urinary tract infections; seven presented after prenatal ultrasonographic diagnosis of hydronephrosis. The location of the ectopic orifice was identified in 25 children: bladder neck (6), posterior urethra (6), vagina (7), and vestibule (6). Upper pole nephroureterectomy was performed in 16 children who had nonfunctioning renal segments. Ureterovesical reimplantation was performed in 10 children who had functioning segments. In five borderline cases, temporary cutaneous ureterostomy was performed, followed by ureteropyelostomy (2), ureterovesical reimplantation (2), and upper pole nephrectomy (1). Histological examination of the polar nephrectomy specimens showed lesions of dysplasia in only four cases (24%). The follow-up period ranged from 6 months to 20 years (mean, 66 months). All children who presented with incontinence became continent after polar nephrectomy or conservative surgery. One child required surgical revision of the ureteropyelostomy anastomosis. Of the 12 children who had ureterovesical reimplantation, none needed further procedures. Ectopic ureters in duplex systems with functioning renal segments should be conserved.

摘要

为评估保守治疗方法的效果,作者回顾了他们对31例完全性输尿管重复畸形合并异位输尿管的治疗经验。1968年至1994年间,对28名女孩和3名男孩(年龄19天至10岁;平均30个月)进行了手术。24名儿童因持续性尿失禁和/或发热性尿路感染前来评估;7名儿童是在产前超声诊断为肾积水后前来就诊。25名儿童确定了异位开口的位置:膀胱颈(6例)、后尿道(6例)、阴道(7例)和前庭(6例)。16名肾功能不全肾段的儿童接受了上极肾输尿管切除术。10名肾功能正常肾段的儿童接受了输尿管膀胱再植术。在5例临界病例中,进行了临时性皮肤输尿管造口术,随后进行了输尿管肾盂吻合术(2例)、输尿管膀胱再植术(2例)和上极肾切除术(1例)。极肾切除术标本的组织学检查仅4例(24%)显示发育异常病变。随访时间为6个月至20年(平均66个月)。所有出现尿失禁的儿童在极肾切除术后或保守手术后均实现了控尿。1名儿童需要对输尿管肾盂吻合术进行手术修复。在接受输尿管膀胱再植术的12名儿童中,无人需要进一步手术。对于具有功能正常肾段的重复系统中的异位输尿管,应予以保留。

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