Diagnosis and classification of Addison's disease (autoimmune adrenalitis)

Autoimmun Rev. 2014 Apr-May;13(4-5):408-11. doi: 10.1016/j.autrev.2014.01.025. Epub 2014 Jan 11.

Abstract

Autoimmune adrenalitis, or autoimmune Addison disease (AAD), is the most prevalent cause of primary adrenal insufficiency in the developed world. AAD is rare and can easily be misdiagnosed as other conditions. The diagnosis depends on demonstrating inappropriately low cortisol production and the presence of high titers of adrenal cortex autoantibodies (ACAs), along with excluding other causes of adrenal failure using other tests as necessary. The treatment corticosteroid replacement, and the prognosis following the treatment is the same as the normal population. Spontaneous recovery of adrenal function has been described but is rare.

Publication types

  • Review

MeSH terms

  • Addison Disease / diagnosis*
  • Addison Disease / epidemiology
  • Addison Disease / etiology
  • Addison Disease / immunology
  • Adrenal Cortex / immunology
  • Adrenal Cortex Hormones / immunology
  • Autoantibodies / immunology
  • Diagnosis, Differential
  • Humans
  • Polyendocrinopathies, Autoimmune / diagnosis
  • Polyendocrinopathies, Autoimmune / immunology

Substances

  • Adrenal Cortex Hormones
  • Autoantibodies