• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[完全性输尿管重复畸形合并输尿管囊肿:两例报告]

[Complete ureteric duplication associated with ureterocele: two cases report].

作者信息

Uchibayashi T, Hisazumi H, Kunimi K, Yamaguchi K, Kawaguchi S, Ohkawa M

出版信息

Hinyokika Kiyo. 1987 Jan;33(1):79-84.

PMID:3577969
Abstract

Herein we report two cases of complete ureteric duplication associated with ureterocele. A 4-month-old girl with non-visualizing left kidney was hospitalized with complaints of cloudy urine and fever. An antegrade left pyelogram revealed a completely duplicated collecting system; a duplex tortuous ureter, and round radiolucent filling defect in the bladder. Under the diagnosis of completely duplicated ureter associated with the upper pole ureterocele, ureterocystoneostomy was performed. A circumferential incision was made around the base of the ureterocele and the Politano-Leadbetter technique was employed. Her postoperative course was uneventful. However, an excretory urogram showed a mild hydronephrotic upper pole. A 1-year and 4-month-old girl with the history of repeated urinary tract infections and fever attacks was admitted. The excretory urogram showed a left hydronephrotic lower pole with a "drooping flower" and no opacification of the upper pole. A radiolucent filling defect was seen in the bladder. A left antegrade pyelogram demonstrated the massively dilated upper pole with a hydroureter terminating in the ureterocele. Left heminephrectomy with partial ureterectomy was performed and left hydronephrosis and hydroureter with an atrophic kidney were seen. The postoperative course was uneventful.

摘要

在此,我们报告两例与输尿管囊肿相关的完全性输尿管重复畸形病例。一名4个月大的女童,左肾不显影,因尿液浑浊和发热入院。顺行性左肾盂造影显示一个完全重复的集合系统;一条双肾盂输尿管迂曲,膀胱内有圆形透光性充盈缺损。在诊断为完全性重复输尿管合并上极输尿管囊肿后,进行了输尿管囊肿膀胱造口术。在输尿管囊肿底部周围做环形切口,并采用Politano-Leadbetter技术。她的术后过程顺利。然而,排泄性尿路造影显示上极有轻度肾积水。一名1岁4个月大的女童,有反复尿路感染和发热发作史,入院。排泄性尿路造影显示左肾下极肾积水呈“下垂花朵”状,上极无造影剂充盈。膀胱内可见透光性充盈缺损。左顺行性肾盂造影显示上极大量扩张,输尿管积水,末端为输尿管囊肿。行左半肾切除术及部分输尿管切除术,可见左肾积水、输尿管积水及萎缩肾。术后过程顺利。

相似文献

1
[Complete ureteric duplication associated with ureterocele: two cases report].[完全性输尿管重复畸形合并输尿管囊肿:两例报告]
Hinyokika Kiyo. 1987 Jan;33(1):79-84.
2
[Ectopic ureterocele of an adult male].
Hinyokika Kiyo. 1984 Oct;30(10):1467-70.
3
[Ectopic ureterocele: a case report].[异位输尿管囊肿:一例报告]
Hinyokika Kiyo. 1984 Sep;30(9):1251-3.
4
[Cecoureterocele. A case report].[膀胱输尿管囊肿。病例报告]
Nihon Hinyokika Gakkai Zasshi. 1989 Dec;80(12):1824-7. doi: 10.5980/jpnjurol1989.80.1824.
5
Endoscopic management of a ureterocele in complete ureteric duplication of an infant.婴儿完全性输尿管重复畸形中输尿管囊肿的内镜治疗
Zhonghua Yi Xue Za Zhi (Taipei). 2002 Mar;65(3):127-30.
6
[A case of inverted Y ureteral duplication with an ectopic ureterocele].
Nihon Hinyokika Gakkai Zasshi. 1992 Oct;83(10):1713-6. doi: 10.5980/jpnjurol1989.83.1713.
7
Ectopic ureterocele without ureteral and calyceal dilatation (ureterocele disproportion): findings on urography and sonography.无输尿管及肾盏扩张的异位输尿管囊肿(输尿管囊肿比例失调):尿路造影和超声检查结果
AJR Am J Roentgenol. 1989 Mar;152(3):567-71. doi: 10.2214/ajr.152.3.567.
8
[A case of ectopic ureterocele in a male adult found during examination of a traumatic injury].
Hinyokika Kiyo. 2004 Apr;50(4):245-8.
9
[The roentgen diagnosis of ureterocele-with special reference to the simple orthotopic ureterocele in adults (author's transl)].输尿管囊肿的X线诊断——特别提及成人单纯原位输尿管囊肿(作者译)
Rontgenblatter. 1981 Jan;34(1):9-14.
10
The unsuspected double collecting system on imaging studies and at cystoscopy.影像学检查及膀胱镜检查中未被发现的重复集合系统。
AJR Am J Roentgenol. 1990 Sep;155(3):561-4. doi: 10.2214/ajr.155.3.2117358.