Metabolic storage diseases: amyloidosis

Clin Liver Dis. 2004 Nov;8(4):915-30, x. doi: 10.1016/j.cld.2004.06.009.

Abstract

This article provides an overview of the current concepts in pathogenesis, epidemiology, clinical significance, and treatment options for amyloidosis. Emphasis is given to hepatic amyloidosis, which ranges from a clinically insignificant histologic curiosity to a harbinger of widespread disease accompanied by a poor prognosis. Clinical characteristics and clues to the diagnosis are discussed as well as the importance of histologic confirmation and the controversy surrounding liver biopsy.

Publication types

  • Review

MeSH terms

  • Amyloidosis / epidemiology
  • Amyloidosis / physiopathology*
  • Amyloidosis / therapy*
  • Biopsy
  • Diagnosis, Differential
  • Humans
  • Incidence
  • Liver / pathology*
  • Prognosis