TY - JOUR
T1 - The clinical implication of monoclonal gammopathies
T2 - Monoclonal gammopathy of undetermined significance and of renal significance
AU - Batko, Krzysztof
AU - Malyszko, Jolanta
AU - Jurczyszyn, Artur
AU - Vesole, David H.
AU - Gertz, Morie A.
AU - Leleu, Xavier
AU - Suska, Anna
AU - Krzanowski, Marcin
AU - Sułowicz, Władysław
AU - Malyszko, Jacek S.
AU - Krzanowska, Katarzyna
N1 - Publisher Copyright:
© 2018 The Author(s) 2018. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - 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.
AB - 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.
KW - Amyloidosis
KW - Kidney function
KW - Monoclonal gammopathy of renal significance
KW - Monoclonal gammopathy of undetermined significance
KW - Multiple myeloma
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U2 - 10.1093/ndt/gfy259
DO - 10.1093/ndt/gfy259
M3 - Review article
C2 - 30169860
AN - SCOPUS:85072041517
SN - 0931-0509
VL - 34
SP - 1440
EP - 1452
JO - Nephrology Dialysis Transplantation
JF - Nephrology Dialysis Transplantation
IS - 9
ER -