轻型输尿管支架置入联合机器人单部位子宫根治术治疗早期宫颈癌1例报告

Chang-Bok Song, Seungmee Lee, H. Chung, T. Jang, S. Kwon, C. Cho
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引用次数: 0

摘要

这是一篇在知识共享署名非商业许可(http://creativecommons.org/ licenses/by-nc/4.0)的条款下发布的开放获取文章,该许可允许在任何媒介上不受限制的非商业使用、分发和复制,前提是正确引用原始作品。对于国际妇产科学联合会(FIGO) IIa1期以下的早期宫颈癌,通常认为主要的治疗方法是手术。FIGO期Ia2至IIa1宫颈癌患者不希望保留生育能力的标准治疗是根治性子宫切除术合并盆腔淋巴结清扫[1,2]。根治性子宫切除术会增加输尿管损伤的风险[3,4]。IRIS U-kit (Stryker, Kalamazoo, MI, USA)是一种轻型输尿管支架,包括用于双侧输尿管的6f半透明输尿管鞘,输尿管鞘内插入光纤,以及光源装置。采用膀胱镜入路将其置于双侧输尿管。它可以在手术中显示双侧输尿管内膜。本实验采用L10 AIM光源(Stryker)。它可以在光纤的尖端产生超过41°C的热量。然而,光纤被放置在输尿管鞘中,这使得它不会直接接触到组织。我们报告了一例机器人辅助的单部位子宫根治术,置入轻型输尿管支架治疗宫颈癌。1例41岁女性FIGO分期Ib1宫颈癌患者行机器人辅助单部位改良根治性子宫切除术(II型)并置入轻型输尿管支架。常规手术悬垂后,采用膀胱镜入路,输尿管鞘插入输尿管各开口20cm。IRIS U-kit (Stryker)的光纤插入输尿管鞘。随后取出膀胱镜。术中两条输尿管均被充分观察。总手术时间105分钟,轻型输尿管支架置入时间7分钟。没有立即或延迟的副作用。轻型输尿管支架置入机器人辅助单点子宫根治术治疗宫颈癌是一种安全可行的选择,有助于克服轻型输尿管支架置入机器人单点子宫根治术在早期宫颈癌治疗中的局限性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case report of lighted ureteral stent insertion with robotic single-site radical hysterectomy in early cervical cancer treatment
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The mainstay of treatment generally considered for early stage cervical cancer below International Federation of Gynecology and Obstetrics (FIGO) stage IIa1 is surgery. The standard treatment for patients from FIGO stage Ia2 to IIa1 cervical cancer who do not wish to preserve fertility is radical hysterectomy with pelvic lymph node dissection [1,2]. During radical hysterectomy, the risk of ureter injury is increased [3,4]. IRIS U-kit (Stryker, Kalamazoo, MI, USA) is a lighted ureteral stent comprising a 6 F translucent ureteral sheath for the bilateral ureters, with optical fibers inserted into the ureteral sheath, and a device for light source. It is placed in the bilateral ureters using cystoscopic approach. It enables the visualization of the bilateral ureter lining during surgery. L10 AIM light source (Stryker) was used in this case. It can generate heat exceeding 41°C at the tip of the optic fiber. However, the optic fiber is placed in the ureteral sheath, which keeps it from coming into direct contact with the tissue. We report a case report of robot assisted single-site radical hysterectomy by inserting lighted ureteral stent for cervical cancer treatment. A 41-year-old woman who was diagnosed with cervical cancer FIGO stage Ib1 underwent robot assisted single-site modified radical hysterectomy (type II) with insertion of lighted ureteral stent. da Vinci Xi Surgical system (Intuitive Surgical, Sunnyvale, CA, USA) platform was used for the surgery. After routine surgical draping, using the cystoscopic approach, ureteral sheath was inserted 20 cm into each ureteral opening. Optic fibers of the IRIS U-kit (Stryker) was inserted into the ureteral sheath. Subsequently, the cystoscope was removed. After installing the lighted ureteral stent, robot docking of the da Vinci Xi surgical system (Intuitive Surgical) was performed followed by radical hysterectomy. Both ureters were fully visualized during the surgery. Total operation time was 105 minutes and time taken for lighted ureteral stent insertion was 7 minutes. There was no immediate or delayed side effect. Lighted ureteral stent insertion in robot assisted singlesite radical hysterectomy for cervical cancer treatment is a safe and feasible option and helps to overcome the limitaCase report of lighted ureteral stent insertion with robotic single-site radical hysterectomy in early cervical cancer treatment
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