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253 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[] Renal histology showed International Society of Nephrology/Renal Pathology Society Class II lupus nephritis.[] Nephrotic syndrome (NS) is a major manifestation of lupus nephritis (LN).[]

  • Familial Mediterranean Fever

    Health specialists may prescribe Col-gout or Colchicine, to help reduce swelling and help prevent systemic amyloidosis.[] She had been diagnosed with lupus nephritis at 19 years old.[] It can also help prevent a serious complication called systemic amyloidosis , which is common in people with FMF. NSAIDs may be used to treat fever and pain.[]

  • 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[] nephritis.[] 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.[]

  • Myopathy

    amyloidosis (32 immunoglobulin light-chain amyloidosis, four familial amyloid polyneuropathy and two senile 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.[]

  • Sicca Syndrome

    The sicca syndrome can be caused by systemic amyloidosis.[] 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.[]

  • Rheumatoid Arthritis

    In Japan, MMF is currently approved for patients with lupus nephritis (LN) and data to indicate its optimal dosage are still insufficient.[] A 46-year-old Japanese woman with rheumatoid arthritis was diagnosed as having systemic lupus erythematosus (SLE) and LN class III (A/C).[]

  • 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[]

  • Hereditary ATTR Amyloidosis

    Amyloidosis is usually a systemic condition, meaning that it affects many organs and systems in the body.[] nephritis, transplant pathology, and newly recognized immunologic and genetic diseases such as ciliopathies, tubulointerstitial nephritis, and glomerulopathies[] […] in hereditary ATTR amyloidosis and ‘wild-type’ ATTR in senile systemic amyloidosis.[]

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