Exp Clin Endocrinol Diabetes 2007; 115(8): 530-532
DOI: 10.1055/s-2007-973077
Case Report

© J. A. Barth Verlag in Georg Thieme Verlag KG · Stuttgart · New York

Long-lasting Subclinical Addison's Disease

S. Torrejón 1 , S. M. Webb 1 , J. Rodríguez-Espinosa 2 , M. J. Martínez de Osaba 3 , R. Corcoy 1
  • 1Department of Endocrinology and Nutrition, Hospital Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain
  • 2Department of Biochemistry, Hospital Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain
  • 3Department of Biochemistry, Hospital Clínic i Provincial, University of Barcelona, Villarroel, Barcelona, Spain
Further Information

Publication History

received 28.09.2006 first decision 12.12.2006

accepted 27.02.2007

Publication Date:
12 September 2007 (online)

Abstract

Objective: To report a patient with autoimmune adrenal disease and increased ACTH with longstanding hyperpigmentation as an isolated symptom.

Methods: A 49-year-old woman requested a diagnostic work-up for hyperpigmentation initiated 9 years before, associated with increased ACTH. She was receiving replacement therapy for autoimmune hypothyroidism. Basal and dynamic tests of glucocorticoid axis, basal investigation of mineralocorticoid axis and measurement of organ specific autoantibodies were performed.

Results: Plasma ACTH (143 pmol/l; normal <13.2 pmol/l) and antibodies against 21-hydroxylase (115 UI/ml; normal <1) were remarkably high, thyroid peroxidase and parietal cell antibodies were positive at low titter and all additional tests were normal.

Conclusion: Autoimmune adrenal disease can have a very long preclinical period even with high concomitant ACTH and specific antibody titers.

References

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Correspondence

S. TorrejónMD 

Servei d'Endocrinologia i Nutrició

Hospital de la Santa Creu I Sant Pau

Sant Antoni M Claret 167

Fax: +34/93/556 57 27

Email: storrejon@gmail.com

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