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Updated: Aug 16, 2026

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
Published on: February 9, 2021
Insights on the pathology of kidney stone formation
Andrew P Evan1, Fredric L Coe, James E Lingeman
1Department of Anatomy and Cell Biology, Indiana University, School of Medicine, Indianapolis, IN, USA. evan@anatomy.iupui.edu
Abstract:
The purpose of these studies was to test the hypothesis that Randall's plaque develops in unique anatomical sites of the kidney and that its formation is conditioned by specific stone-forming pathophysiologies. To test this hypothesis, we performed intraoperative mapping studies with biopsies of papilla from the kidneys of 15 idiopathic calcium oxalate (CaOx) stone formers, four intestinal bypass for obesity patients and ten brushite stone formers, and obtained papillary specimens from four non-stone formers after nephrectomy. Both light and electron microscopic examination of tissue changes along with infrared and electron diffraction analyses of mineral composition were performed. Distinct patterns of mineral deposition and papillary pathology were discovered in each of the three different stone forming groups. CaOx stone formers had predictable sites of interstitial apatite crystals beginning at the thin loops of Henle and spreading to the urothelium. These plaque areas are termed Randall's plaque and are thought to serve as sites for stone attachment. The papilla and medullary tubules appeared normal. The intestinal bypass patients only had intraluminal sites of crystalline material in the medullary collecting ducts. The brushite stone formers had the most severe form of cortical and medullary changes with sites of Randall's plaque, and yellowish intraluminal deposits in medullary collecting ducts. All deposits were determined to be apatite. The metabolic and surgical pathologic finding in three distinct groups of stone formers clearly shows that "the histology of the renal papilla from a stone former is particular to the clinical setting". It is observations like these that we believe will provide the insights to allow the stone community to generate better clinical treatments for kidney stone disease, as we understand the pathogenesis of stone formation for each type of stone former.
Insights
Randall's plaque formation varies by kidney stone type. Different pathophysiologies lead to distinct mineral deposits and papillary changes, crucial for understanding kidney stone disease.
Area of Science:
- Nephrology
- Urology
- Pathology
Background:
- Kidney stone formation is a complex process.
- Randall's plaque is implicated in stone pathogenesis.
- Understanding plaque development is key to targeted therapies.
Purpose of the Study:
- To investigate if Randall's plaque forms in specific kidney locations.
- To determine if distinct stone-forming conditions influence plaque development.
- To correlate renal papilla histology with clinical stone type.
Main Methods:
- Intraoperative mapping and biopsy of renal papilla from various stone formers and controls.
- Light and electron microscopy for tissue analysis.
- Infrared and electron diffraction for mineral composition identification.
Main Results:
- Idiopathic calcium oxalate stone formers showed interstitial apatite crystals (Randall's plaque) originating in Henle's loops.
- Intestinal bypass patients exhibited intraluminal crystalline material in medullary collecting ducts.
- Brushite stone formers presented severe cortical/medullary changes and Randall's plaque.
Conclusions:
- Renal papilla histology is specific to the clinical setting of stone formation.
- Distinct pathophysiologies result in unique Randall's plaque locations and compositions.
- These findings offer insights for developing tailored treatments for different kidney stone types.
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