Treatment of light chain deposition disease with bortezomib and dexamethasone
Efstathios Kastritis, Magdalini Migkou, Maria Gavriatopoulou, P. Zirogiannis, Valsamakis Hadjikonstantinou, Meletios Α. Dimopoulos
Abstract
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Efstathios Kastritis, Magdalini Migkou, Maria Gavriatopoulou, P. Zirogiannis, Valsamakis Hadjikonstantinou, Meletios Α. Dimopoulos
Abstract
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Light chain deposition disease (LCDD) is a rare plasma cell dyscrasia characterized by deposition of immunoglobulin fragments. The kidneys are almost always affected while heart, liver and other tissues are occasionally involved. About 50% of patients with LCDD have concurrent myeloma, however most
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Light chain deposition disease (LCDD) is a rare plasma cell dyscrasia characterized by deposition of immunoglobulin fragments. The kidneys are almost always affected while heart, liver and other tissues are occasionally involved. About 50% of patients with LCDD have concurrent myeloma, however most
Key concepts: Plasma cell dyscrasia, Paraproteinemias, Immunoglobulin light chain, Dyscrasia, Multiple myeloma, Bortezomib, Plasma cell, Medicine