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236 Possible Causes for Lupus Nephritis, Systemic Amyloidosis

  • Systemic Lupus Erythematosus

    Oct 2016 Familial amyloid polyneuropathy (FAP) is a rare inherited autosomal dominant form of systemic amyloidosis, which classically presents with severe motor, sensory,[] Class V Membranous lupus nephritis Global or segmental sub-epithelial immune deposits Class VI Advanced sclerotic lupus nephritis 90% of glomeruli globally sclerosed without[] lupus nephritis is permanent renal damage.[]

  • Nephrotic Syndrome

    It occurs in glomerular disease and thrombosis of a renal vein and as a complication of many systemic diseases, diabetes mellitus, amyloidosis, systemic lupus erythematosus[] These can include: membranous nephropathy, focal segmental glomerulosclerosis, minimal change disease, membranoproliferative glomerulonephritis, lupus nephritis, and IgA nephropathy[] It generally affects more men than women although lupus nephritis is common in women. It affects more adult than children with an estimated adult:child ratio of 26:1.[]

  • Renal Amyloidosis

    Systemic amyloidosis complicating multidrug-resistant tuberculosis in childhood. Pediatric Infectious Disease Journal 2012; 31(9): 994-997.[] The patient was admitted to the Internal Medicine Department to evaluate the etiology of the nephrotic syndrome, among which the possibilities were: lupus nephritis, amyloidosis[] RA Kyle , MA Gertz : Primary systemic amyloidosis: Clinical and laboratory features in 474 cases Semin Hematol 32: 45 – 59 , 1995 Medline 13.[]

  • Lipoid Nephrosis

    Systemic lupus erythematosus. This chronic inflammatory disease can lead to serious kidney damage. Amyloidosis.[] The natural history and treatment of lupus nephritis, in Lewis EJ, Schwartz MM, Korbet SM (eds): Lupus Nephritis. Oxford, Oxford University Press 1999;pp 185-218. 31.[] […] diabetes , systemic lupus erythematosus , multiple myeloma , and amyloidosis .[]

  • Diffuse Scleroderma

    […] sclerosis, polymyositis, and SLE Overlap syndromes Systemic sclerosis plus polymyositis, rheumatoid arthritis, or SLE Scleroderma mimics Amyloidosis Chronic graft-versus-host[] Intravenous immunoglobulin compared with cyclophosphamide for proliferative lupus nephritis. Lancet 1999 ; 354 : 569 –70. 6 Cherin P, Herson S, Wechsler B et al .[] Amyloidosis . Chronic graft-versus-host disease . Paraneoplastic syndromes. General approach to management [ 1 ] There is no cure for SSc.[]

  • Acute Glomerulonephritis

    Lupus Erythematosus (SLE); Amyloidosis; Diabetic glomerulopathy; HIV-associated nephropathy; Sickle-Cell disease The onset of symptoms for GN occur about 10 days from the[] Secondary causes of diffuse GN include the following: Cryoglobulinemia Goodpasteur’s syndrome (membranous antiglomerular basement membrane disease) Lupus nephritis Schönlein-Henoch[] Skin rashes (ie, malar rash frequently seen with lupus nephritis) may be observed.[]

  • Myopathy

    Amyloidosis can involve both the central nervous system and peripheral nerves. Amyloid myopathy is a rare manifestation of primary systemic amyloidosis.[] Immune-Mediated Necrotizing Myopathy, Associated With Antibodies to Signal Recognition Particle, Together With Lupus Nephritis: Case Presentation and Management.[] Toxins Alcohol Toluene Myopathy Associated with Systemic Diseases Endocrine disorders Thyroid Parathyroid Pituitary or adrenal dysfunction Systemic inflammatory diseases Systemic[]

  • Monoclonal Gammopathy of Undetermined Significance

    Three of these patients also had primary systemic amyloidosis.[] Immune complex-mediated glomerular lesions, such as IgA nephropathy, membranous nephropathy, and lupus nephritis, are well documented to be caused by the deposition of polyclonal[] Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989.Blood. 1992;79:1817-22.[]

  • Primary Sclerosing Cholangitis

    PSC might initiate amyloid A protein deposition in diverse tissues, giving rise to systemic amyloidosis, due to a progressive and unresolved inflammatory process, and its[] […] erythematosus (SLE), lupus nephritis, autoimmune haemolytic anaemia, idiopathic thrombocytopenic purpura, Langerhans cell histiocytosis, membranous nephropathy, Peyronie's[] The proper treatment of PSC complicated by systemic Amyloid A amyloidosis remains to be determined. [ 22 ] Cholangiocarcinoma reportedly occurs in association with PSC in[]

  • Hereditary ATTR Amyloidosis

    Senile Systemic Amyloidosis (wild type ATTR amyloidosis ) Senile systemic amyloidosis (wild type ATTR amyloidosis ) is a slowly progressive disease.[] nephritis, transplant pathology, and newly recognized immunologic and genetic diseases such as ciliopathies, tubulointerstitial nephritis, and glomerulopathies[] Amyloidosis is usually a systemic condition, meaning that it affects many organs and systems in the body.[]

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