首页> 美国卫生研究院文献>Journal of Endourology Case Reports >Subcapsular Splenic Urinoma and Splenorenal Fistula: A New Complication of Percutaneous Nephrolithotomy
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Subcapsular Splenic Urinoma and Splenorenal Fistula: A New Complication of Percutaneous Nephrolithotomy

机译:荚膜下脾泌尿系统瘤和脾肾瘘:经皮肾镜取石术的新并发症

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摘要

>Background: Splenic urinoma has not been previously reported as a complication of percutaneous nephrolithotomy (PNL).>Case Presentation: A 46-year-old Caucasian male underwent PNL for two large left renal stones. Surgery was performed in prone split-leg position, with access obtained through combined fluoroscopic guidance and direct ureteroscopic observation of the targeted calix. The tract was dilated to 30F using a pressure balloon, and complete clearance of stones was obtained through a combination of rigid and flexible nephroscopy, as well as antegrade ureteroscopy. The patient was left with a Double-J ureteral stent on a string for removal in 1 week. After overnight observation, his hemoglobin, white blood cell count, and renal function were normal and thus he was discharged home. The day after stent removal, he presented to the emergency department with abdominal pain, was found to have mild left hydronephrosis on CT, and was discharged on 1 week of antibiotics. One week later he re-presented with worsening abdominal pain and was found to have an elevated creatinine and a white blood cell count of 21 × 109/L. On contrasted CT with delayed images, an 18 cm splenic fluid collection was seen with a fistulous connection to the left kidney collecting system. He underwent emergent stent placement and improved clinically without drainage of the urinoma. A renal ultrasonography 1 month after stent placement confirmed resolution of the splenic urinoma, so the stent was removed at 1 month. Follow-up CT 1 month after stent removal was normal without any evidence of fistula or urinoma recurrence.>Conclusion: This is the first report of a subcapsular splenic urinoma and splenorenal fistula post-PNL. Ureteral stent placement was sufficient for drainage and to resolve the complication.
机译:>背景:以前尚未报道脾脏尿路上皮瘤是经皮肾镜取石术(PNL)的并发症。>病例介绍:一名46岁的白人男性接受了左侧两个大的PNL肾结石。手术在俯卧的双腿位置进行,通过结合荧光透视引导和直接输尿管镜观察目标杯的获得。使用压力气球将尿道扩张至30F,并通过刚性和柔性肾镜检查以及顺行输尿管镜检查获得结石的完全清除。将该患者留在弦上的Double-J输尿管支架在1周内取出。过夜观察后,他的血红蛋白,白细胞计数和肾功能正常,因此出院了。取出支架后的第二天,他因腹痛出现在急诊科,被发现在CT上有轻度左肾积水,并在服用抗生​​素1周后出院。一周后,他再次表现出腹痛加剧,并发现肌酐升高,白细胞计数为21×10 9 / L。在具有延迟图像的CT对比中,看到18 cm的脾液集合与左肾集合系统有瘘管连接。他接受了紧急支架置入,并在临床上得到了改善,没有引流尿道瘤。支架置入后1个月的肾脏超声检查证实脾脏尿路上皮瘤已消退,因此在1个月时取下了支架。支架拆除后1个月的随访CT正常,没有任何瘘管或尿路上皮瘤复发的证据。>结论:这是PNL后囊状脾下尿路上皮瘤和脾肾瘘的首次报道。输尿管支架放置足以引流并解决并发症。

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