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Monoclonal gammopathy of renal significance: Multidisciplinary approach to diagnosis and treatment.
Karam, Sabine; Haidous, Mohammad; Dalle, Iman Abou; Dendooven, Amélie; Moukalled, Nour; Van Craenenbroeck, Amaryllis; Bazarbachi, Ali; Sprangers, Ben.
Afiliação
  • Karam S; Division of Nephrology and Hypertension, University of Minnesota, Minneapolis, MN, United States.
  • Haidous M; Department of Medicine, Saint Vincent Charity Medical Center, Cleveland, OH, United States.
  • Dalle IA; Bone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Dendooven A; Department of Pathology, University Hospital Ghent, Ghent, Belgium.
  • Moukalled N; Bone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Van Craenenbroeck A; Department of Microbiology, Immunology and Transplantation, Laboratory of Nephrology, KU Leuven, Leuven, Belgium; Division of Nephrology, University Hospitals Leuven, Leuven, Belgium.
  • Bazarbachi A; Bone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon; Department of Anatomy, Cell Biology and Physiological Sciences, American University of Beirut Medical Center, Beirut, Lebanon.
  • Sprangers B; Biomedical Research Institute, Department of Immunology and Infection, University Hasselt, Diepenbeek, Belgium; Department of Nephrology, Ziekenhuis Oost-Limburg, Genk, Belgium. Electronic address: ben.sprangers@zol.be.
Crit Rev Oncol Hematol ; 183: 103926, 2023 Mar.
Article em En | MEDLINE | ID: mdl-36736510
Monoclonal gammopathy of renal significance (MGRS) is a hemato-nephrological term referring to a heterogeneous group of kidney disorders characterized by direct or indirect kidney injury caused by a monoclonal immunoglobulin (MIg) produced by a B cell or plasma cell clone that does not meet current hematologic criteria for therapy. MGRS-associated kidney diseases are diverse and can result in the development of end stage kidney disease (ESKD). The diagnosis is typically made by nephrologists through a kidney biopsy. Many distinct pathologies have been identified and they are classified based on the site or composition of the deposited Mig, or according to histological and ultrastructural findings. Therapy is directed towards the identified underlying clonal population and treatment decisions should be coordinated between hematologists and nephrologists in a multidisciplinary fashion, depend on the type of MGRS, the degree of kidney function impairment and the risk of progression to ESKD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraproteinemias / Gamopatia Monoclonal de Significância Indeterminada / Nefropatias / Falência Renal Crônica Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraproteinemias / Gamopatia Monoclonal de Significância Indeterminada / Nefropatias / Falência Renal Crônica Idioma: En Ano de publicação: 2023 Tipo de documento: Article