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

IF 0.5 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
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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.

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微创治疗先天性腔静脉后输尿管1例。
下腔静脉后输尿管(RU)是一种罕见的先天性畸形,其中输尿管通路改变,向后绕过下腔静脉(IVC)。有时,这会导致下腔静脉压迫输尿管,导致梗阻。在这篇报告中,我们讨论了一位男性,他表现出严重的右侧腹部疼痛,其他方面都很好,没有明显的医学、泌尿学或出生史。初步影像显示严重右侧输尿管伴明显梗阻点,可能为RU。回顾了轶事和小中心病例的急性管理和腹腔镜RU修复。最初的治疗重点是疼痛控制,需要肾造口术,随后经腹膜腹腔镜解剖和修复。手术时间138 min,出血量50 mL。术后患者恢复良好,超声随访6个月无症状。同样,大多数回顾的病例选择经腹膜腹腔镜入路,效果良好。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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