Renal hilar tumor with situs inversus- a case report and systematic review

IF 0.4 Q4 UROLOGY & NEPHROLOGY Urology Case Reports Pub Date : 2025-05-01 Epub Date: 2025-01-16 DOI:10.1016/j.eucr.2025.102955
Chong Yan , Gang Li , Zi-Hao Li , Ze-Hua Wei , Yu-Xin Peng , Yi-Fang Tao , Tie Chong , Zhen-Long Wang
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Abstract

Total situs inversus is a rare congenital condition (1 in 25,000) with mirror-image organ positioning, complicating nephrectomies. A 68-year-old female with situs inversus presented with a right renal hilum mass incidentally discovered. Imaging revealed a tumor difficult to distinguish from the renal artery and an elongated right renal vein mimicking left-sided anatomy. Radical nephrectomy achieved favorable recovery and preserved renal function. Reviewing 14 cases (1987–2024), focus has shifted to anatomical variations, especially vascular anomalies, affecting surgical complexity. Preoperative imaging to assess adjacent structures is crucial for optimizing surgical approaches and ensuring patient safety.
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肾门部肿瘤伴倒位1例报告及系统回顾
全倒位是一种罕见的先天性疾病(25,000分之一),伴有镜像器官定位,使肾切除术复杂化。一位68岁女性逆位患者,偶然发现右肾门肿块。影像显示一个难以与肾动脉区分的肿瘤和一个细长的右肾静脉,模仿左侧解剖结构。根治性肾切除术取得了良好的恢复和保存肾功能。回顾14例病例(1987-2024),重点转移到解剖变异,特别是血管异常,影响手术复杂性。术前影像学评估邻近结构是优化手术入路和确保患者安全的关键。
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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