Calcium oxalate crystal deposition in the kidney: identification, causes and consequences

被引:31
作者
Geraghty, R. [1 ]
Wood, K. [2 ]
Sayer, J. A. [1 ,3 ,4 ]
机构
[1] Newcastle Hosp NHS Fdn Trust, Renal Serv, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[2] Newcastle Hosp NHS Fdn Trust, Histopathol Dept, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[3] Newcastle Univ, Int Ctr Life, Fac Med Sci, Translat & Clin Res Inst, Cent Pkwy, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[4] NIHR Newcastle Biomed Res Ctr, Newcastle Upon Tyne, Tyne & Wear, England
关键词
Calcium oxalate; Oxalosis; Primary hyperoxaluria; Enteric hyperoxaluria; RENAL GRAFT FAILURE; Y GASTRIC BYPASS; PRIMARY HYPEROXALURIA; OXALOBACTER-FORMIGENES; EPITHELIAL-CELLS; DIETARY OXALATE; NEPHROPATHY; NEPHROLITHIASIS; EXCRETION; PATIENT;
D O I
10.1007/s00240-020-01202-w
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Calcium oxalate (CaOx) crystal deposition within the tubules is often a perplexing finding on renal biopsy of both native and transplanted kidneys. Understanding the underlying causes may help diagnosis and future management. The most frequent cause of CaOx crystal deposition within the kidney is hyperoxaluria. When this is seen in native kidney biopsy, primary hyperoxaluria must be considered and investigated further with biochemical and genetic tests. Secondary hyperoxaluria, for example due to enteric hyperoxaluria following bariatric surgery, ingested ethylene glycol or vitamin C overdose may also cause CaOx deposition in native kidneys. CaOx deposition is a frequent finding in renal transplant biopsy, often as a consequence of acute tubular necrosis and is associated with poorer long-term graft outcomes. CaOx crystal deposition in the renal transplant may also be secondary to any of the causes associated with this phenotype in the native kidney. The pathophysiology underlying CaOx deposition is complex but this histological phenotype may indicate serious underlying pathology and should always warrant further investigation.
引用
收藏
页码:377 / 384
页数:8
相关论文
共 89 条
[1]   Renal function can be impaired in children with primary hyperoxaluria type 3 [J].
Allard, Lise ;
Cochat, Pierre ;
Leclerc, Anne-Laure ;
Cachat, Francois ;
Fichtner, Christine ;
De Souza, Vandrea Carla ;
Garcia, Clotilde Druck ;
Camoin-Schweitzer, Marie-Christine ;
Macher, Marie-Alice ;
Acquaviva-Bourdain, Cecile ;
Bacchetta, Justine .
PEDIATRIC NEPHROLOGY, 2015, 30 (10) :1807-1813
[2]   Rare crystalline nephropathy leading to acute graft dysfunction: a case report [J].
Bagai, Sahil ;
Khullar, Dinesh ;
Bansal, Bhavna .
BMC NEPHROLOGY, 2019, 20 (01)
[3]   Oxalate deposits in biopsies from native and transplanted kidneys, and impact on graft function [J].
Bagnasco, Serena M. ;
Mohammed, Basim S. ;
Mani, Haresh ;
Gandolfo, Maria Teresa ;
Haas, Mark ;
Racusen, Lorraine C. ;
Montgomery, Robert A. ;
Kraus, Edward .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2009, 24 (04) :1319-1325
[4]   Early recurrence of oxalate deposition after renal transplantation in a patient with primary hyperoxaluria type I [J].
Bilgin, N ;
Tirnaksiz, MB ;
Moray, G ;
Karakayali, H ;
Yildirim, S ;
Demirhan, B ;
Haberal, M .
TRANSPLANTATION PROCEEDINGS, 1999, 31 (08) :3219-3220
[5]   Oxalate Nephropathy Associated with Chronic Pancreatitis [J].
Cartery, Claire ;
Faguer, Stanislas ;
Karras, Alexandre ;
Cointault, Olivier ;
Buscail, Louis ;
Modesto, Anne ;
Ribes, David ;
Rostaing, Lionel ;
Chauveau, Dominique ;
Giraud, Patrick .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (08) :1895-1902
[6]   Species differences in Cl- affinity and in electrogenicity of SLC26A6-mediated oxalate/Cl- exchange correlate with the distinct human and mouse susceptibilities to nephrolithiasis [J].
Clark, Jeffrey S. ;
Vandorpe, David H. ;
Chernova, Marina N. ;
Heneghan, John F. ;
Stewart, Andrew K. ;
Alper, Seth L. .
JOURNAL OF PHYSIOLOGY-LONDON, 2008, 586 (05) :1291-1306
[7]   The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II [J].
Cramer, SD ;
Ferree, PM ;
Lin, K ;
Milliner, DS ;
Holmes, RP .
HUMAN MOLECULAR GENETICS, 1999, 8 (11) :2063-2069
[8]   Enteric hyperoxaluria: A hidden cause of early renal graft failure in two successive transplants: Spontaneous late graft recovery [J].
Cuvelier, C ;
Goffin, E ;
Cosyns, J ;
Wauthier, M ;
de Strihou, CV .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 40 (01)
[9]   PEROXISOMAL ALANINE - GLYOXYLATE AMINOTRANSFERASE DEFICIENCY IN PRIMARY HYPEROXALURIA TYPE-I [J].
DANPURE, CJ ;
JENNINGS, PR .
FEBS LETTERS, 1986, 201 (01) :20-24
[10]  
Daudon M, 2004, ANN BIOL CLIN-PARIS, V62, P379