Membranous Glomerulopathy With Light Chain–Restricted Deposits: A Clinicopathological Analysis of 28 Cases
Membranous glomerulopathy (MG) is a common cause of nephrotic syndrome that results from the formation of immune complexes along the subepithelial aspect of the glomerular basement membranes. Although it is most frequently caused by polytypic deposits, cases with light chain isotype−restricted depos...
Main Authors: | Alejandro Best Rocha, Christopher P. Larsen |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-11-01
|
Series: | Kidney International Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2468024917303157 |
Similar Items
-
Clinicopathologic Features of Membranous-Like Glomerulopathy With Masked IgG Kappa Deposits
by: C.P. Larsen, et al.
Published: (2016-11-01) -
Successful treatment with bortezomib and dexamethasone for proliferative glomerulonephritis with monoclonal IgG deposits in multiple myeloma: a case report
by: Rio Noto, et al.
Published: (2017-04-01) -
A case of immunotactoid glomerulopathy with false-negative IgG staining
by: Shuma Hirashio, et al.
Published: (2018-06-01) -
A case of immunotactoid glomerulopathy in a patient with monoclonal gammopathy of renal significance
by: Victoria Campdesuner, et al.
Published: (2021-01-01) -
Monoclonal light chain crystalline podocytopathy and tubulopathy associated with monoclonal gammopathy of renal significance: a case report and literature review
by: Xiao-juan Yu, et al.
Published: (2018-11-01)