双侧单系统异位输尿管伴输尿管膨出:一例罕见的成年男性

Harjinder Singh, A. Singla, Anahat Kaur
{"title":"双侧单系统异位输尿管伴输尿管膨出:一例罕见的成年男性","authors":"Harjinder Singh, A. Singla, Anahat Kaur","doi":"10.14740/WJNU162W","DOIUrl":null,"url":null,"abstract":"Bilateral single system ectopic ureter (BSSEU) is a rare congenital malformation. We report a case of BSSEU with a rare association of ectopic ureter with contralateral ectopic sphinctero-stenotic ureterocele with agenesis of one seminal vesicle with normal urinary continence and fertility presenting in adulthood as a case of chronic kidney disease. Diagnosis of ureterocele was missed even after detailed radiological investigations, so concurrent endoscopic evaluation is important for final diagnosis and operative intervention. As renal functions were markedly deranged, so transurethral incision of the right ureterocele with double J stenting was done as a preliminary procedure. Renal functions improved subsequently. Patient is planned for left nephroureterectomy and if necessary right ureteric reimplantation as a secondary major surgery in the follow-up period. World J Nephrol Urol. 2014;3(2):103-105 doi: http://dx.doi.org/10.14740 /wjnu162w","PeriodicalId":91634,"journal":{"name":"World journal of nephrology and urology","volume":"3 1","pages":"103-105"},"PeriodicalIF":0.0000,"publicationDate":"2014-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bilateral Single System Ectopic Ureters With Ureterocele: A Rare Association in an Adult Male\",\"authors\":\"Harjinder Singh, A. Singla, Anahat Kaur\",\"doi\":\"10.14740/WJNU162W\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bilateral single system ectopic ureter (BSSEU) is a rare congenital malformation. We report a case of BSSEU with a rare association of ectopic ureter with contralateral ectopic sphinctero-stenotic ureterocele with agenesis of one seminal vesicle with normal urinary continence and fertility presenting in adulthood as a case of chronic kidney disease. Diagnosis of ureterocele was missed even after detailed radiological investigations, so concurrent endoscopic evaluation is important for final diagnosis and operative intervention. As renal functions were markedly deranged, so transurethral incision of the right ureterocele with double J stenting was done as a preliminary procedure. Renal functions improved subsequently. Patient is planned for left nephroureterectomy and if necessary right ureteric reimplantation as a secondary major surgery in the follow-up period. World J Nephrol Urol. 2014;3(2):103-105 doi: http://dx.doi.org/10.14740 /wjnu162w\",\"PeriodicalId\":91634,\"journal\":{\"name\":\"World journal of nephrology and urology\",\"volume\":\"3 1\",\"pages\":\"103-105\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World journal of nephrology and urology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14740/WJNU162W\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of nephrology and urology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14740/WJNU162W","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

摘要双侧单系统异位输尿管是一种罕见的先天性畸形。我们报告一例罕见的BSSEU伴异位输尿管伴对侧异位括约肌-狭窄性输尿管精索膨出伴一个精囊缺失伴正常尿失禁和生育能力在成年期表现为慢性肾病的病例。即使经过详细的放射检查,也会遗漏输尿管囊肿的诊断,因此同时进行内镜评估对最终诊断和手术干预很重要。由于肾功能明显紊乱,因此初步采用经尿道右输尿管囊肿切开双J型支架置入。随后肾功能改善。患者计划行左肾输尿管切除术,必要时行右输尿管再植术作为随访期间的二次大手术。世界肾炎杂志,2014;3(2):103-105 doi: http://dx.doi.org/10.14740 /wjnu162w
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bilateral Single System Ectopic Ureters With Ureterocele: A Rare Association in an Adult Male
Bilateral single system ectopic ureter (BSSEU) is a rare congenital malformation. We report a case of BSSEU with a rare association of ectopic ureter with contralateral ectopic sphinctero-stenotic ureterocele with agenesis of one seminal vesicle with normal urinary continence and fertility presenting in adulthood as a case of chronic kidney disease. Diagnosis of ureterocele was missed even after detailed radiological investigations, so concurrent endoscopic evaluation is important for final diagnosis and operative intervention. As renal functions were markedly deranged, so transurethral incision of the right ureterocele with double J stenting was done as a preliminary procedure. Renal functions improved subsequently. Patient is planned for left nephroureterectomy and if necessary right ureteric reimplantation as a secondary major surgery in the follow-up period. World J Nephrol Urol. 2014;3(2):103-105 doi: http://dx.doi.org/10.14740 /wjnu162w
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信