A case report of minimally invasive management of congenital retrocaval ureter.

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2025-03-12 eCollection Date: 2025-03-01 DOI:10.1093/jscr/rjaf134
Orna T Cantillon, Ibrahim Haidaran, Ned Kinnear, Derek B Hennessey
{"title":"A case report of minimally invasive management of congenital retrocaval ureter.","authors":"Orna T Cantillon, Ibrahim Haidaran, Ned Kinnear, Derek B Hennessey","doi":"10.1093/jscr/rjaf134","DOIUrl":null,"url":null,"abstract":"<p><p>Retrocaval ureter (RU) is a rare congenital malformation where the ureteric pathway is altered, passing posteriorly around the inferior vena cava (IVC). Occasionally, this leads to the IVC compressing the ureter, resulting in obstruction. In this report, we discuss a male who presented with severe right-sided flank pain and was otherwise well with no significant medical, urological, or birth history. Initial imaging revealed severe right-sided hydroureter with distinct obstruction point, and likely RU. Anecdotal and small centre cases of acute management and laparoscopic RU repair were reviewed. Initial management focused on pain control requiring a nephrostomy with subsequent transperitoneal laparoscopic dissection and repair. Operative time was 138 min with 50 mL blood loss. Post-operatively the patient recovered well and was symptom free at 6 month follow up ultrasound. Similarly, most reviewed cases chose a trans-peritoneal laparoscopic approach with good outcomes.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 3","pages":"rjaf134"},"PeriodicalIF":0.4000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11903002/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Surgical Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/jscr/rjaf134","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

Abstract

Retrocaval ureter (RU) is a rare congenital malformation where the ureteric pathway is altered, passing posteriorly around the inferior vena cava (IVC). Occasionally, this leads to the IVC compressing the ureter, resulting in obstruction. In this report, we discuss a male who presented with severe right-sided flank pain and was otherwise well with no significant medical, urological, or birth history. Initial imaging revealed severe right-sided hydroureter with distinct obstruction point, and likely RU. Anecdotal and small centre cases of acute management and laparoscopic RU repair were reviewed. Initial management focused on pain control requiring a nephrostomy with subsequent transperitoneal laparoscopic dissection and repair. Operative time was 138 min with 50 mL blood loss. Post-operatively the patient recovered well and was symptom free at 6 month follow up ultrasound. Similarly, most reviewed cases chose a trans-peritoneal laparoscopic approach with good outcomes.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
相关文献
The Expulsion of Muslims from Spain
IF 0.4 Digest of Middle East StudiesPub Date : 1992-10-01 DOI: 10.1111/J.1949-3606.1992.TB00387.X
Abbas Hamdani
来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
期刊最新文献
Radiofrequency sacroplasty as a pain treatment for symptomatic sacral destruction due to prostate metastasis: a case report and a review of the literature. A case report of minimally invasive management of congenital retrocaval ureter. Case series of high pressure paint injection injuries in single digits in a tertiary referral centre over a one year period. Decision making in surgery: honoring patient autonomy despite high mortality risk in a 36-year-old woman with endocarditis. Gallbladder perforation due to the obstructing periampullary duodenal diverticulum (Lemmel's syndrome): a case report.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1