The evaluation of monoclonal gammopathy of renal significance: a consensus report of the International Kidney and Monoclonal Gammopathy Research Group

被引:0
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作者
Nelson Leung
Frank Bridoux
Vecihi Batuman
Aristeidis Chaidos
Paul Cockwell
Vivette D. D’Agati
Angela Dispenzieri
Fernando C. Fervenza
Jean-Paul Fermand
Simon Gibbs
Julian D. Gillmore
Guillermo A. Herrera
Arnaud Jaccard
Dragan Jevremovic
Efstathios Kastritis
Vishal Kukreti
Robert A. Kyle
Helen J. Lachmann
Christopher P. Larsen
Heinz Ludwig
Glen S. Markowitz
Giampaolo Merlini
Peter Mollee
Maria M. Picken
Vincent S. Rajkumar
Virginie Royal
Paul W. Sanders
Sanjeev Sethi
Christopher P. Venner
Peter M. Voorhees
Ashutosh D. Wechalekar
Brendan M. Weiss
Samih H. Nasr
机构
[1] Division of Nephrology,Department of Nephrology
[2] Hematology,Veterans Administration Medical Center, New Orleans, LA
[3] Department of Laboratory Medicine and Pathology,Centre for Haematology, Department of Medicine
[4] Mayo Clinic,Department of Pathology, Renal Pathology Laboratory
[5] Centre Hospitalier Universitaire et Université de Poitiers,Department of Haematology and Immunology
[6] Poitiers,National Amyloidosis Centre, Centre for Amyloidosis and Acute Phase Proteins, Division of Medicine, Royal Free Campus
[7] France; CNRS UMR7276,Department of Pathology and Translational Pathobiology
[8] Limoges,Department of Clinical Therapeutics
[9] France; and Centre de Référence Amylose AL et Autres Maladies par Dépôt d’Immunoglobulines Monoclonales,Amyloidosis Research and Treatment Center, IRCCS Policlinico San Matteo
[10] USA and Tulane University Medical School,Haematology Department, Princess Alexandra Hospital and School of Medicine
[11] Imperial College London and Imperial College Healthcare NHS Trust,Department of Pathology
[12] Hammersmith Hospital,Department of Pathology, Hôpital Maisonneuve
[13] Department of Nephrology,Rosemont
[14] Renal Medicine — University Hospitals Birmingham NHS Foundation Trust,Department of Medicine
[15] Queen Elizabeth Hospital,Cross Cancer Institute
[16] Columbia University,Department of Hematologic Oncology and Blood Disorders
[17] College of Physicians and Surgeons,Abramson Cancer Center
[18] University Hospital St Louis,undefined
[19] The Victorian and Tasmanian Amyloidosis Service,undefined
[20] Department of Haematology,undefined
[21] Monash Univerity Easter Health Clinical School,undefined
[22] University College London,undefined
[23] Louisiana State University Health Sciences Center,undefined
[24] Service d’Hématologie et de Thérapie Cellulaire,undefined
[25] Centre de Référence des Amyloses Primitives et des Autres Maladies par Dépôts d’Immunoglobuline,undefined
[26] CHU Limoges,undefined
[27] School of Medicine National and Kapodistrian University of Athens Alexandra Hospital,undefined
[28] University Health Network,undefined
[29] Princess Margaret Cancer Centre,undefined
[30] Arkana Laboratories,undefined
[31] Wilhelminen Cancer Research Institute,undefined
[32] Wilhelminenspital,undefined
[33] University of Pavia,undefined
[34] University of Queensland,undefined
[35] Loyola University Medical Center,undefined
[36] Université de Montreal,undefined
[37] Montreal,undefined
[38] University of Alabama at Birmingham and Department of Veterans Affairs Medical Center,undefined
[39] University of Alberta,undefined
[40] Levine Cancer Institute,undefined
[41] Atrium System,undefined
[42] University of Pennsylvania,undefined
[43] Perelman School of Medicine,undefined
来源
Nature Reviews Nephrology | 2019年 / 15卷
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摘要
The term monoclonal gammopathy of renal significance (MGRS) was introduced by the International Kidney and Monoclonal Gammopathy Research Group (IKMG) in 2012. The IKMG met in April 2017 to refine the definition of MGRS and to update the diagnostic criteria for MGRS-related diseases. Accordingly, in this Expert Consensus Document, the IKMG redefines MGRS as a clonal proliferative disorder that produces a nephrotoxic monoclonal immunoglobulin and does not meet previously defined haematological criteria for treatment of a specific malignancy. The diagnosis of MGRS-related disease is established by kidney biopsy and immunofluorescence studies to identify the monotypic immunoglobulin deposits (although these deposits are minimal in patients with either C3 glomerulopathy or thrombotic microangiopathy). Accordingly, the IKMG recommends a kidney biopsy in patients suspected of having MGRS to maximize the chance of correct diagnosis. Serum and urine protein electrophoresis and immunofixation, as well as analyses of serum free light chains, should also be performed to identify the monoclonal immunoglobulin, which helps to establish the diagnosis of MGRS and might also be useful for assessing responses to treatment. Finally, bone marrow aspiration and biopsy should be conducted to identify the lymphoproliferative clone. Flow cytometry can be helpful in identifying small clones. Additional genetic tests and fluorescent in situ hybridization studies are helpful for clonal identification and for generating treatment recommendations. Treatment of MGRS was not addressed at the 2017 IKMG meeting; consequently, this Expert Consensus Document does not include any recommendations for the treatment of patients with MGRS.
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页码:45 / 59
页数:14
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