机器人辅助腹腔镜肾盂成形术后肾盂淋巴瘘致乳糜尿的内镜治疗。

Q4 Medicine
Journal of Endourology Case Reports Pub Date : 2020-12-29 eCollection Date: 2020-01-01 DOI:10.1089/cren.2020.0160
Andrew Rabley, Jonathan Pavlinec, Elizabeth Kwenda, Jennifer Kuo, Lawrence Yeung
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引用次数: 0

摘要

背景:乳糜尿是一种罕见的诊断,通常与乳白色的尿液有关。它包括乳糜渗漏到泌尿道。虽然世界范围内乳糜尿最常见的原因是感染性的,但也有其他非感染性的病因。乳糜尿通常会自发或保守治疗。手术治疗已被描述,但通常不需要。我们报告一例医源性肾盂淋巴瘘后,机器人辅助腹腔镜肢解肾盂成形术,并在内镜下电瘘道治疗。病例介绍:一名50岁的白人男性接受了机器人辅助的腹腔镜肢解肾盂成形术并植入支架,影像学显示左侧肾盂输尿管连接处梗阻。术后随访4周,患者开始注意到间歇性乳白色尿液排出。尿液分析显示蛋白质含量高,尿中甘油三酯升高。最初对他进行了保守的饮食调整,但没有成功。然后他接受了内窥镜治疗,膀胱镜和输尿管镜检查,疑似肾盂淋巴瘘。术后住院1周,患者维持低脂中链甘油三酯饮食和奥曲肽注射。术后病程无明显变化,无乳糜尿复发。术后9个月乳糜尿消失。结论:机器人辅助腹腔镜肾盂成形术后的肾盂淋巴瘘是肾周夹层的一种理论上的并发症,以前的文献中没有描述过。它应该被认为是乳糜尿的罕见医源性原因。内窥镜治疗电灼在技术上是可行的,可以避免更多的侵入性手术治疗的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endoscopic Management of Chyluria Caused by Pyelolymphatic Fistula After Robot-Assisted Laparoscopic Pyeloplasty.

Background: Chyluria is a rare diagnosis classically associated with milky-appearing urine. It involves the leakage of chyle into the urinary tract. Although the most common cause of chyluria worldwide is infectious in nature, other noninfectious etiologies have been described. Classically chyluria resolves spontaneously or with conservative management. Surgical treatments have been described but are not often required. We present a case of iatrogenic pyelolymphatic fistula after robot-assisted laparoscopic dismembered pyeloplasty that was treated with endoscopic electrocautery of the fistulous tract. Case Presentation: A 50-year-old Caucasian man underwent a robot-assisted laparoscopic dismembered pyeloplasty with stent insertion for radiographically demonstrated left ureteropelvic junction obstruction. His postoperative course was uneventful until 4-week follow-up at which time he began to notice intermittent passage of milky-appearing urine. Urinalysis was notable for large protein and elevated urine triglycerides. He was initially managed conservatively dietary modifications without success. He then underwent endoscopic management with cystoscopy and ureteroscopy with fulguration of suspected pyelolymphatic fistula. He was maintained on a low-fat medium-chain triglyceride diet and octreotide injections while inpatient for 1 week postoperatively. His postoperative course was unremarkable and no return of chyluria was observed. His chyluria remained resolved at 9 months postoperatively. Conclusion: Pyelolymphatic fistula after robot-assisted laparoscopic pyeloplasty is a theoretical complication of perirenal dissection and has not been previously described in the literature. It should be considered as a rare iatrogenic cause of chyluria. Endoscopic management with fulguration is technically feasible and may obviate the need for more invasive surgical management.

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