Primary systemic amyloidosis

Archana Roy, Vivek Roy

Research output: Contribution to journalReview article

10 Scopus citations


Primary systemic amyloidosis is a rare disease with protean manifestations. Presence of nephrotic syndrome in the absence of diabetes and hypertension, cardio-myopathy in the absence of isch-emia, restrictive cardiac defect, demyelinating polyneuropathy, or unexplained hepatomegaly should alert the physician to the possibility of amyloidosis. Initial steps in the diagnostic evaluation of patients with suspected amyloidosis include serum and urine immunoelectrophoresis and immunofixation studies. Demonstration of amyloid material on tissue biopsy (eg, subcutaneous fat) is required for diagnosis. Availability of effective treatments has improved the outlook of patients with primary systemic amyloidosis. Early diagnosis is critical to optimizing the chances of effective therapy.

Original languageEnglish (US)
JournalPostgraduate medicine
Issue number1
StatePublished - Jan 1 2006


ASJC Scopus subject areas

  • Medicine(all)

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