Document Type
Report
Publication Date
5-16-2023
Abstract
Severe hyperlipidemia warrants an extensive evaluation. We report a case of a 25-year-old man of Chinese descent seen in the cardiology-lipid clinic. He was found to have a serum low-density lipoprotein cholesterol of 12.12 mmol/L (468 mg/dL) and serum triglycerides of 2.29 mmol/L (203 mg/dL) during routine screening. Work-up revealed nephrotic-range proteinuria, and renal biopsy showed dilated glomerular capillary loops with lipid deposits, pathognomonic of lipoprotein glomerulopathy. Genetic studies showed apolipoprotein E3/E4 phenotype. He was treated with a high-intensity statin and fibrate therapy, which resulted in a marked improvement in dyslipidemia and proteinuria.
Recommended Citation
Tito, Sahana; Atri, Avica; Patil, Shivaraj; Dean, Saima; and Carpenter, Sweta, "Apolipoprotein E Dyslipidemia and Nephrotic Syndrome: A Rare Connection" (2023). Einstein Health Papers. Paper 30.
https://jdc.jefferson.edu/einsteinfp/30
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Language
English
Included in
Cardiology Commons, Internal Medicine Commons, Nephrology Commons
Comments
This article is the author's final published version in Annals of Internal Medicine Clinical Cases, Volume 2, Issue 5, May 2023, Article number e230059.
The published version is available at https://doi.org/10.7326/aimcc.2023.0059.
Copyright © 2023 Authors.