Secondary glomerular disease occurs when the glomeruli in the kidneys are injured by systemic diseases or diverse mechanisms. Some examples that can cause secondary glomerular disease include lupus nephritis from systemic lupus erythematosus, diabetic nephropathy from damage caused by high blood sugar in diabetes, and amyloidosis which can result from immunoglobulin light chain deposits or serum amyloid A protein fragments. Other systemic diseases that can lead to secondary glomerular disease are multiple myeloma, Goodpasture syndrome, microscopic polyangiitis, Wegener granulomatosis, Henoch-Schonlein purpura, bacterial endocarditis, and thrombotic microangiopathy.
Secondary glomerular disease occurs when the glomeruli in the kidneys are injured by systemic diseases or diverse mechanisms. Some examples that can cause secondary glomerular disease include lupus nephritis from systemic lupus erythematosus, diabetic nephropathy from damage caused by high blood sugar in diabetes, and amyloidosis which can result from immunoglobulin light chain deposits or serum amyloid A protein fragments. Other systemic diseases that can lead to secondary glomerular disease are multiple myeloma, Goodpasture syndrome, microscopic polyangiitis, Wegener granulomatosis, Henoch-Schonlein purpura, bacterial endocarditis, and thrombotic microangiopathy.
Secondary glomerular disease occurs when the glomeruli in the kidneys are injured by systemic diseases or diverse mechanisms. Some examples that can cause secondary glomerular disease include lupus nephritis from systemic lupus erythematosus, diabetic nephropathy from damage caused by high blood sugar in diabetes, and amyloidosis which can result from immunoglobulin light chain deposits or serum amyloid A protein fragments. Other systemic diseases that can lead to secondary glomerular disease are multiple myeloma, Goodpasture syndrome, microscopic polyangiitis, Wegener granulomatosis, Henoch-Schonlein purpura, bacterial endocarditis, and thrombotic microangiopathy.
Secondary glomerular disease occurs when the glomeruli in the kidneys are injured by systemic diseases or diverse mechanisms. Some examples that can cause secondary glomerular disease include lupus nephritis from systemic lupus erythematosus, diabetic nephropathy from damage caused by high blood sugar in diabetes, and amyloidosis which can result from immunoglobulin light chain deposits or serum amyloid A protein fragments. Other systemic diseases that can lead to secondary glomerular disease are multiple myeloma, Goodpasture syndrome, microscopic polyangiitis, Wegener granulomatosis, Henoch-Schonlein purpura, bacterial endocarditis, and thrombotic microangiopathy.
Secondary glomerular disease : Glomeruli injured by diverse mechanisms and in the
course of a number systemic diseases.
Glomerulopathies Secondary to Systemic Diseases :
1. Lupus Nephritis (Systemic Lupus Erythematosus) Lupus causes inflammation in the kidneys 2. Diabetic Nephropathy With diabetes, the small blood vessels in the body are injured. When the blood vessels in the kidneys are injured, it can’t clean blood properly. High level of blood sugar High blood volume Kidney overworked Diabetes may cause damage to nerves Difficulty in emptying bladder Full bladder causing pressure back up & injure kidney 3. Amyloidosis Most renal amyloidosis is either the result of primary fibrillar deposits of immunoglobulin light chains [amyloid L (AL)], or secondary to fibrillar deposits of serum amyloid A (AA) protein fragments 4. Glomerular Nephropathy Secondary to Multiple Myeloma 5. Goodpasture syndrome Goodpasture syndrome describe the clinical entity of diffuse pulmonary hemorrhage and acute or rapidly progressive glomerulonephritis. Anti-GBM disease 6. Microscopic polyangiitis Vasculitis of small vessels, which can damage organ systems 7. Wegener granulomatosis A rare multisystem autoimmune disease of unknown etiology. Its hallmark features include necrotizing granulomatous inflammation and pauci-immune vasculitis in small- and medium-sized blood vessels 8. Henoch-Schonlein Purpura Henoch-Schönlein purpura (HSP) is an acute immunoglobulin A (IgA)- mediated disorder characterized by a generalized vasculitis involving the small vessels of the skin, the gastrointestinal (GI) tract, the kidneys, the joints, and, rarely, the lungs and the central nervous system (CNS) 9. Bacterial Endocarditis – related GN 10.Thrombotic Microangiopathy