Add to ORKGLight chain deposit disease is a plasma cell disorder characterized by production of a large amount of monoclonal immunoglobulin light chain or part of it, which is usually deposited as an amorphous substance in the kidneys. Immunotactoid glomerulopathy is an uncommon disease, which might be related to plasma cell dyscrasia, and characteristically manifest as organized glomerular ultra structural fibrils or microtubules. In this article, we report a case of a combined presentation of light chain disease and immunotactoid glomerulopathy in a patient with multiple myeloma and reversible advanced renal failure
Membranous glomerulopathy (MG) is a common cause of nephrotic syndrome that results from the formati...
Abstract Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and pe...
International audienceLight chain deposition disease (LCDD) is a rare disorder characterized by glom...
Abstract. The pathologic manifestations of renal diseases related to monoclonal plasma cell dyscrasi...
Light Chain Deposition Disease (LCDD) is a type of monoclonal immunoglobulin deposition disease char...
Light chain deposition disease (LCDD), a rare form of monoclonal gammopathy, is characterized by dep...
Monoclonal gammopathies consist of a broad spectrum of diseases, ranging from asymptomatic monoclona...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
Light Chain Deposition Disease (LCDD) is a relatively frequent renal disease associated with dysprot...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
An autopsy case of light chain deposition disease is reported here. A 60-year-old female with plasma...
Introduction. Immunoglobulin D (IgD) myeloma is a rare disease, about 2% of all myelomas, even ra...
Abstract Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and pe...
Abstract Light chain deposition disease (LCDD) is a rare clinical entity characterized by the deposi...
Membranous glomerulopathy (MG) is a common cause of nephrotic syndrome that results from the formati...
Abstract Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and pe...
International audienceLight chain deposition disease (LCDD) is a rare disorder characterized by glom...
Abstract. The pathologic manifestations of renal diseases related to monoclonal plasma cell dyscrasi...
Light Chain Deposition Disease (LCDD) is a type of monoclonal immunoglobulin deposition disease char...
Light chain deposition disease (LCDD), a rare form of monoclonal gammopathy, is characterized by dep...
Monoclonal gammopathies consist of a broad spectrum of diseases, ranging from asymptomatic monoclona...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
Light Chain Deposition Disease (LCDD) is a relatively frequent renal disease associated with dysprot...
8 pagesLight-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases...
An autopsy case of light chain deposition disease is reported here. A 60-year-old female with plasma...
Introduction. Immunoglobulin D (IgD) myeloma is a rare disease, about 2% of all myelomas, even ra...
Abstract Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and pe...
Abstract Light chain deposition disease (LCDD) is a rare clinical entity characterized by the deposi...
Membranous glomerulopathy (MG) is a common cause of nephrotic syndrome that results from the formati...
Abstract Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and pe...
International audienceLight chain deposition disease (LCDD) is a rare disorder characterized by glom...