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Amyloidosis


Amyloidosis The definitive test is the demonstration of amyloid in a tissue biopsy , using special stains, IF and EM. Ideally, biopsy of an affected organ (eg liver, kidney) should be performed. If no specific site can be identified, colorectal biopsy or gingival biopsy may demonstrate amyloid. Further tests may assist in determining nature and cause: FBC , CRP or ESR , protein electrophoresis - serum , protein electrophoresis - urine ; paraprotein typing - serum if an immunoglobulin origin is suspected; immunoglobulins G, A, M ; bone marrow aspiration and trephine biopsy . Creatinine, urea, protein (urine) to assess renal involvement.
  Immunoglobulin origin  
    Primary amyloidosis  
    Multiple myeloma  
  Amyloid A origin  
    Chronic inflammation esp  
      Chronic infection  
      Rheumatoid arthritis  
    Familial Mediterranean fever  
  Pre-albumin origin  
    Familial amyloid polyneuropathy Molecular genetics , if available.
  b2-microglobulin origin
    Dialysis-associated
 
Beta-2-microglobulin - serum .
  Localised deposition  
    Cerebral  
      Alzheimer’s disease See under Dementia .
    Laryngeal  
    Bladder  
    Tumour associated eg  
      Medullary carcinoma of thyroid See under Thyroid nodule/cyst .
    Senile eg  
      Cardiac  
      Cerebral  





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