Kuo Ramsay L, Lingeman James E, Evan Andrew P, Paterson Ryan F, Bledsoe Sharon B, Kim Samuel C, Munch Larry C, Coe Fredric L
Methodist Hospital Institute for Kidney Stone Disease and Indiana University School of Medicine, Indianapolis, USA.
J Urol. 2003 Dec;170(6 Pt 1):2186-9. doi: 10.1097/01.ju.0000096065.61481.35.
The mechanisms behind calcium nephrolithiasis remain unclear. Previous research has relied on animal models or cell lines, yielding limited insight into the pathophysiology of human calcium stone disease. To determine changes occurring in the human kidney during active stone disease we used an endoscopic renal papillary biopsy protocol in calcium stone formers undergoing percutaneous nephrolithotomy.
Following stone burden clearance via percutaneous nephrolithotomy 15 idiopathic calcium oxalate and 4 ileal bypass stone formers underwent flexible and rigid nephroscopy. Biopsies from select papillae in the peripheral and interpolar regions were obtained with 5Fr flexible cup biopsy forceps. A papilla adjacent to the accessed calix was biopsied with 10Fr cup biopsy forceps. Cortical biopsies along the access tract were also obtained with the 10Fr forceps.
All patients had successful biopsy completion. No complications were attributable to the biopsy process and no blood transfusions were required. Of the 19 patients 12 were contacted for followup at a mean of 21.7 +/- 9.0 months with none experiencing adverse sequelae such as bleeding or significant pain. A total of 14 patients had followup serum creatinine available showing that the difference in mean preoperative and postoperative values was not clinically significant (1.00 +/- 0.27 and 1.11 +/- 0.27 mg/dl, respectively). The quality of biopsied tissue permitted accurate immunohistochemical staining of crystal deposits and mineral analysis.
Endoscopic papillary biopsies were performed safely in a small patient population. Tissue obtained using this protocol can be used for detailed histological and analytical studies, which may lead to significant advances in our understanding of stone formation mechanisms.
钙肾结石形成背后的机制仍不清楚。以往的研究依赖于动物模型或细胞系,对人类钙结石病的病理生理学了解有限。为了确定活动性结石病期间人类肾脏发生的变化,我们对接受经皮肾镜取石术的钙结石患者采用了内镜肾乳头活检方案。
通过经皮肾镜取石术清除结石负荷后,15例特发性草酸钙结石患者和4例回肠旁路结石患者接受了软性和硬性肾镜检查。使用5Fr软性杯状活检钳从外周和极间区域的选定乳头获取活检组织。用10Fr杯状活检钳对靠近进入肾盏的乳头进行活检。还使用10Fr活检钳沿着进入通道获取皮质活检组织。
所有患者活检均成功完成。活检过程未导致并发症,也无需输血。19例患者中有12例在平均21.7±9.0个月时接受了随访,均未出现出血或严重疼痛等不良后遗症。共有14例患者有随访血清肌酐数据,显示术前和术后平均值的差异无临床意义(分别为1.00±0.27和1.11±0.27mg/dl)。活检组织的质量允许对晶体沉积物进行准确的免疫组织化学染色和矿物质分析。
在内镜下对一小部分患者进行乳头活检是安全的。使用该方案获得的组织可用于详细的组织学和分析研究,这可能会在我们对结石形成机制的理解上取得重大进展。