Khan Saeed R
Department of Pathology and Center for the Study of Lithiasis, College of Medicine, University of Florida, Gainesville, FL, USA.
Urol Res. 2006 Apr;34(2):86-91. doi: 10.1007/s00240-005-0016-2. Epub 2006 Jan 11.
Supersaturation is the driving force behind crystal formation in the kidneys. It can, however, result only in the formation of crystals which can be harmlessly expelled. For stone formation, crystals must form in the kidneys and be retained there, which is indeed a rare occurrence. Crystalluria is common while stone formation is not. Only pathological changes in the kidneys including renal injury and dysfunction can accomplish crystal retention. Lethal epithelial cellular injury promotes crystal nucleation, aggregation and retention. Sub-lethal injury or dysfunctional cells may produce ineffective crystallization modulators and localized areas of supersaturation in the interstitium. The former will affect crystallization in the urine while the latter may cause precipitation in the interstitium and development of Randall's plaques.
过饱和是肾脏中晶体形成的驱动力。然而,它只会导致形成能够无害排出的晶体。对于结石形成而言,晶体必须在肾脏中形成并留存于此处,但这种情况确实很少见。结晶尿很常见,而结石形成并不常见。只有包括肾损伤和功能障碍在内的肾脏病理变化才能实现晶体留存。致死性上皮细胞损伤会促进晶体成核、聚集和留存。亚致死性损伤或功能失调的细胞可能会产生无效的结晶调节剂,并在间质中形成局部过饱和区域。前者会影响尿液中的结晶,而后者可能会导致间质中的沉淀以及兰德尔斑的形成。