Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
Main Article Content
ABSTRACT
Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day). However, nephrotic syndrome and proliferative glomerulonephritis are uncommon in patients with polycystic kidney disease. Development of nephrotic syndrome and / or rapid deterioration in kidney function suggest the presence of another, more aggressive disorder, requiring prompt diagnosis and appropriate interventions to mitigate further injury and progression to end stage kidney disease. In this chapter, we will discuss rapidly progressive glomerulonephritis in association with ADPKD.
Downloads
Metrics
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Copyright of individual chapters belongs to the respective authors. The authors grant unrestricted publishing and distribution rights to the publisher. The electronic versions of the chapters are published under Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Users are allowed to share and adapt the chapters for any non-commercial purposes as long as the authors and the publisher are explicitly identified and properly acknowledged as the original source. The books in their entirety are subject to copyright by the publisher. The reproduction, modification, republication and display of the books in their entirety, in any form, by anyone, for commercial purposes are strictly prohibited without the written consent of the publisher.