2008
DOI: 10.2215/cjn.01600408
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Renal Lesions Associated with IgM-Secreting Monoclonal Proliferations

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Cited by 93 publications
(85 citation statements)
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“…These include myeloma kidney (cast nephropathy), AL amyloidosis, and light-chain deposition disease (13). The spectrum of renal lesions associated with monoclonal gammopathy is extensive (14) and depends on the physiochemical properties of the Ig produced. Of the 2603 native renal biopsies done at the Mayo Clinic from 2001 through 2006, 239 showed AL amyloidosis (9.16%), 30 showed myeloma kidney (1.3%), 48 showed light-chain deposition disease (1.8%), and only one showed heavy-chain deposition disease.…”
Section: Discussionmentioning
confidence: 99%
“…These include myeloma kidney (cast nephropathy), AL amyloidosis, and light-chain deposition disease (13). The spectrum of renal lesions associated with monoclonal gammopathy is extensive (14) and depends on the physiochemical properties of the Ig produced. Of the 2603 native renal biopsies done at the Mayo Clinic from 2001 through 2006, 239 showed AL amyloidosis (9.16%), 30 showed myeloma kidney (1.3%), 48 showed light-chain deposition disease (1.8%), and only one showed heavy-chain deposition disease.…”
Section: Discussionmentioning
confidence: 99%
“…Thrombotic microangiopathy, typically limited to the kidney, can result from Ig-induced endothelial injury as well as systemic chemotherapy or stem cell transplantation used to treat myeloma (18). Monoclonal IgM, which is a much larger molecule than IgG, can produce hyperviscosityassociated renal impairment and additionally form deposits that occlude glomerular capillaries (19). Monoclonal IgA can result in IgA nephopathy or Henoch-Schonlein purpura, although this result is uncommon (20).…”
Section: Mechanisms Of Myeloma and Plasma Cell-associated Kidney Injurymentioning
confidence: 99%
“…The incidence of renal complications of malignant IgMsecreting proliferation has decreased, mostly because of improved treatment of WM, the major cause of those nephropathies. Audard et al (62), who recently revisited the disease spectrum, showed that GN with intracapillary thrombi of IgM, originally described by Morel-Maroger et al as Waldenström macroglobulinemic glomerulonephritis (55), was not specific for WM and suggested that the term intracapillary monoclonal deposits disease may be more appropriate in this context.…”
Section: Hematologic Malignancy-induced Paraneoplastic Glomerulopathimentioning
confidence: 99%