Kidney stone formers have more renal parenchymal crystals than non-stone formers, particularly in the papilla region

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Kidney stone formers have more renal parenchymal crystals than non-stone formers, particularly in the papilla region

BACKGROUND We investigated the renoprotective ability of healthy people against kidney stone formation. To clarify intratubular crystal kinetics and processing in human kidneys, we performed a quantitative and morphological observation of nephrectomized renal parenchyma tissues. METHODS Clinical data and pathological samples from 60 patients who underwent radical nephrectomy for renal cancer ...

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Do Kidney Stone Formers Have A Kidney Disease?

Nephrolithiasis is a highly prevalent disorder affecting approximately one in eleven people and is associated with multiple complications including hypertension, cardiovascular disease, and chronic kidney disease. Significant epidemiologic associations with chronic kidney disease and ESRD have been noted and are reviewed herein, but debate persists in the literature as to whether kidney stone f...

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Chronic kidney disease in kidney stone formers.

Recent population studies have found symptomatic kidney stone formers to be at increased risk for chronic kidney disease (CKD). Although kidney stones are not commonly identified as the primary cause of ESRD, they still may be important contributing factors. Paradoxically, CKD can be protective against forming kidney stones because of the substantial reduction in urine calcium excretion. Among ...

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Percutaneous renal biopsy specimens in stone formers.

A series of renal biopsy specimens taken at the time of percutaneous nephrolithotomy were investigated for the presence and location of foci of microcalcification. Calcium was found in 18 of 25 (72%) of biopsy specimens from stone formers and in only seven of 30 (23%) of control biopsy specimens. This may indicate defective intrarenal handling of calcium as plasma calcium concentration was norm...

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Screening for CLCN5 mutation in renal calcium stone formers patients.

UNLABELLED Thirty-five patients (23 males and 12 females), age 35 +/- 13 years old, presenting either idiopathic calcium nephrolithiasis, nephrocalcinosis or mild renal failure with idiopathic calcium nephrolithiasis were selected for the analysis of low molecular weight proteinuria and the possible mutations occurrence in the chloride channel gene CLCN5. The urinary ratio of beta2-microglobuli...

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ژورنال

عنوان ژورنال: BMC Urology

سال: 2018

ISSN: 1471-2490

DOI: 10.1186/s12894-018-0331-x