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Bilateral hand-assisted laparoscopic nephrectomy for autosomal dominant polycystic kidney disease using a single midline HandPort incision.

机译:使用单中线HandPort切口进行双侧手助腹腔镜肾切除术治疗常染色体显性多囊肾疾病。

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OBJECTIVES: To present one of the first known series of bilateral, transperitoneal laparoscopic nephrectomy for autosomal dominant polycystic kidney disease using a hand-assisted technique by way of a single, midline HandPort incision. Synchronous, bilateral nephrectomy for autosomal dominant polycystic kidney disease is an infrequently performed procedure, with only a few reports using laparoscopy. METHODS: We retrospectively reviewed the charts of 4 patients undergoing bilateral hand-assisted laparoscopic nephrectomy for symptomatic autosomal dominant polycystic kidney disease between June 2000 and January 2001. Follow-up consisted of chart review and telephone survey. RESULTS: All 4 patients underwent successful bilateral hand-assisted laparoscopic nephrectomy, with a mean operative time of 286 minutes. This included 1 patient who underwent simultaneous laparoscopic marsupialization of symptomatic hepatic cysts. The average size of the polycystic kidneys removed was 1582 g. Complications included acute tubular necrosis of a renal allograft in 1 patient that resolved spontaneously and retained retroperitoneal cystic fluid that required percutaneous drainage in another patient. All patients did well postoperatively, with complete resolution of their presenting symptoms. Those with renal allografts had stable function at the last follow-up visit. CONCLUSIONS: Bilateral hand-assisted laparoscopic nephrectomy using a single HandPort incision is a feasible alternative for the removal of symptomatic polycystic kidneys. It offers the advantage of easier identification and control of hilar structures that are often obscured by the distorted renal anatomy. In addition, it allows the simultaneous performance of other intra-abdominal procedures.
机译:目的:介绍一种使用手辅助技术通过单条中线HandPort切口进行常染色体显性多囊肾疾病的双侧经腹腔镜双侧腹腔镜肾切除术。常染色体显性多囊肾疾病的同步双侧肾切除术是一种不常进行的手术,只有少数报道使用腹腔镜检查。方法:我们回顾性回顾了2000年6月至2001年1月间4例因有症状的常染色体显性遗传性多囊肾病接受双侧手腹腔镜肾切除术的患者的病历。随访包括病历复查和电话调查。结果:全部4例患者均成功进行了双侧手腹腔镜肾切除术,平均手术时间为286分钟。其中包括1例同时进行了有症状肝囊肿的腹腔镜有袋化术的患者。取出的多囊肾的平均大小为1582 g。并发症包括1例患者的同种异体肾移植急性肾小管坏死,其自然消退并保留了腹膜后囊性积液,而另一名患者需要经皮引流。所有患者术后表现良好,症状完全缓解。接受肾脏同种异体移植的患者在最后一次随访中功能稳定。结论:使用单HandPort切口进行双侧手辅助腹腔镜肾切除术是去除有症状的多囊肾的可行选择。它具有易于识别和控制经常被扭曲的肾脏解剖结构掩盖的肺门结构的优势。另外,它允许同时执行其他腹腔内手术。

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