Collagenofibrotic glomerulopathy in a kidney transplant recipient: A first report

被引:0
作者
Jdiaa, Sara S. [1 ]
Moeckel, Gilbert W. [2 ]
Kfoury, Hala M. [3 ]
Medawar, Walid A. [1 ]
Abu-Alfa, Ali K. [1 ,4 ]
机构
[1] Amer Univ Beirut, Fac Med, Dept Internal Med, Div Nephrol & Hypertens, Beirut, Lebanon
[2] Yale Univ, Sch Med, Dept Pathol, Div Renal Pathol & Electron Microscopy, New Haven, CT 06510 USA
[3] Amer Univ Beirut, Fac Med, Dept Pathol & Lab Med, Div Anat Pathol, Beirut, Lebanon
[4] Yale Univ, Sch Med, Dept Internal Med, Sect Nephrol, New Haven, CT USA
关键词
clinical research; practice; genetics; kidney transplantation; nephrology; recurrent disease; III GLOMERULOPATHY; COLLAGEN; PATELLA;
D O I
10.1111/ajt.16399
中图分类号
R61 [外科手术学];
学科分类号
摘要
Collagenofibrotic glomerulopathy (CG) is a rare disease characterized by the deposition of collagen type 3 fibrils in the glomeruli. Patients may have proteinuria, hematuria, and/or renal dysfunction. CG is considered a progressive disease with variable rates of progression. The definitive diagnosis is made by electron microscopy with the presence of characteristic subendothelial and mesangial curved, comma-like, banded collagen type 3 fibers of 40-65 nm periodicity. We are reporting the first case of CG in a kidney transplant recipient with kidney disease of unknown cause.
引用
收藏
页码:1948 / 1952
页数:5
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