Paraprotein-related kidney disease: Diagnosing and treating monoclonal gammopathy of renal significance

36Citations
Citations of this article
99Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Paraprotein-related kidney disease represents a complex group of diseases caused by an abnormal paraprotein secreted by a clone of B cells. The diseasemanifestations range from tubulopathies, such as the Fanconi syndrome, to a spectrum of glomerular diseases that can present with varying degrees of proteinuria and renal dysfunction. Diagnosis of these diseases can be challenging because of the wide range ofmanifestations as well as the relatively common finding of a serum paraprotein, especially in elderly patients. Thus, renal biopsy along with detailed hematologic workup is essential to link the presence of the paraprotein to the associated renal disease. Recent advances in treatment withmore effective and targeted chemotherapies, as well as stemcell transplantation, have improved the renal and overall prognosis for many of these disorders.

Cite

CITATION STYLE

APA

Rosner, M. H., Edeani, A., Yanagita, M., Glezerman, I. G., & Leung, N. (2016). Paraprotein-related kidney disease: Diagnosing and treating monoclonal gammopathy of renal significance. Clinical Journal of the American Society of Nephrology, 11(12), 2280–2287. https://doi.org/10.2215/CJN.02920316

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free