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243 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,[] What is lupus nephritis? There are two types of lupus.[] The results suggest that lupus nephritis might be associated with physical activity.[]

  • 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[] Nephrotic syndrome (NS) is a major manifestation of lupus nephritis (LN).[] Lupus-like HIVICK is treated differently than 'true' lupus nephritis, so distinction is warranted.[]

  • 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[] Patients with lupus nephritis may have a normal serum creatinine value Patients with lupus nephritis may require multiple sequential biopsies In lupus nephritis a fall in[] Certain illnesses are known to trigger acute GN, including: strep throat systemic lupus erythematosus , which is also called lupus Goodpasture syndrome , a rare autoimmune[]

  • Lipoid Nephrosis

    Systemic lupus erythematosus. This chronic inflammatory disease can lead to serious kidney damage. Amyloidosis.[] It was also of interest that peripheral blood lymphocytes (PBL) from 3 patients with lupus nephritis (SLE) produced significantly low levels of TCFC.[] 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.[]

  • 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.[]

  • Sicca Syndrome

    Immunoglobulin light-chain (AL) amyloidosis is a form of systemic amyloidosis in which the fibrils are derived from monoclonal light chains.[] Two patients developed overlapping lupus nephritis or autoimmune hepatitis years following diagnosis of SS.[] It can affect the kidneys in various ways including interstitial nephritis, kidney stones or glomerulonephritis.[]

  • Myopathy

    Amyloidosis can involve both the central nervous system and peripheral nerves. Amyloid myopathy is a rare manifestation of primary systemic amyloidosis.[] CASE REPORT A 35-year-old woman with a past medical history of hypothyroidism, systemic lupus erythematosus (SLE), and end-stage renal disease secondary to lupus nephritis[] Immune-Mediated Necrotizing Myopathy, Associated With Antibodies to Signal Recognition Particle, Together With Lupus Nephritis: Case Presentation and Management.[]

  • Renal Amyloidosis

    The kidney is the most commonly affected organ by systemic amyloidosis.[] 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[] In an attempt to standardize pathology reports for renal amyloidosis similar to the lupus nephritis classification, a classification system has been proposed that is based[]

  • 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.[]

  • 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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