The clinical implication of monoclonal gammopathies: monoclonal gammopathy of undetermined significance and of renal significance

Author:

Batko Krzysztof1,Malyszko Jolanta2,Jurczyszyn Artur3,Vesole David H4,Gertz Morie A5,Leleu Xavier6,Suska Anna3,Krzanowski Marcin1,Sułowicz Władysław1,Malyszko Jacek S7,Krzanowska Katarzyna1

Affiliation:

1. Departament of Nephrology, Jagiellonian University Medical College, Kraków, Poland

2. Department of Nephrology, Dialysis and Internal Medicine, Warsaw Medical University, Warszawa, Poland

3. Departament of Hematology, Jagiellonian University Medical College, Kraków, Poland

4. Myeloma DIvision, John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ, USA

5. Division of Hematology, Mayo Clinic, Rochester, MN, USA

6. Service d`Hematologie CHU, Hopital de la Miletrie, Poitiers, France

7. 1st Department of Nephrology, Medical University, Bialystok, Poland

Abstract

Abstract Monoclonal gammopathy of renal significance (MGRS) has introduced a new perspective to several well-known disease entities impacting nephrology, haematology and pathology. Given the constantly changing disease spectrum of these entities, it is clinically imperative to establish diagnostic and treatment pathways supported by evidence-based medicine. MGRS is a disease of the kidney, secondary to plasma cell clonal proliferation or immune dysfunction, requiring therapeutic intervention to eradicate the offending clone. To fully understand the disease(s), it is prerequisite to determine the significance of the findings. The diagnostic work up should be extensive due to the wide heterogeneity of clinical presentation, ultimately necessitating kidney biopsy. Particular patient profiles such as AL amyloidosis, which may be diagnosed through biopsies of other tissues/organs, may be an exception. Treatment decisions should be formulated by multi-disciplinary consensus: nephrologists, haematologists and pathologists. The ultimate goal in managing MGRS is eradication of the offending plasma cell clone which requires targeted chemotherapy and, in eligible cases, haematopoietic stem cell transplantation. We present a review of diagnostic procedures, treatment options and advances in the last few years in the management of MGRS in an effort to acquaint specialists with this new face of several older diseases.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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