A Rare Case of Lipoprotein Glomerulopathy in a White Man: An Emerging Entity in Asia, Rare in the White Population

Author:

Boumendjel Redouane1,Papari Mona1,Gonzalez Miguel1

Affiliation:

1. From the Department of Pathology, University of Illinois, Chicago (Drs Boumendjel and Papari); and the Department of Pathology, Advocate Lutheran General Hospital, Park Ridge, Illinois (Dr Gonzalez)

Abstract

Abstract Lipoprotein glomerulopathy is a rare entity that predominantly affects the Asian population, mainly the Japanese and Chinese. Lipoprotein glomerulopathy is clinically characterized by proteinuria and progression to renal failure and is caused by glomerular lipoprotein thrombi formation in association with increased levels of serum apolipoprotein E. The disease has a male predominance and can affect virtually any age group. We describe the third reported case, to our knowledge, of lipoprotein glomerulopathy to affect a white patient.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Lipoprotein Glomerulopathy, First Case Report from Canada;International Journal of Nephrology and Renovascular Disease;2022-06

2. An Updated Review and Meta Analysis of Lipoprotein Glomerulopathy;Frontiers in Medicine;2022-05-06

3. Glomerular Diseases;Diagnostic Atlas of Renal Pathology;2017

4. Glomerular Diseases;Diagnostic Atlas of Renal Pathology;2012

5. All-trans retinoic acid regulates the expression of apolipoprotein E in rats with glomerulosclerosis induced by Adriamycin;Experimental and Molecular Pathology;2011-06

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