Published 2 July 2009, doi:10.1136/bmj.b2385
Cite this as: BMJ 2009;339:b2385

Practice

Easily Missed?

Addison’s disease

Bijay Vaidya, consultant endocrinologist, honorary senior clinical lecturer1,2, Ali J Chakera, specialist registrar1, Catherine Dick, general practitioner3

1 Department of Endocrinology, Royal Devon and Exeter Hospital, Exeter EX2 5DW, 2 Peninsula Medical School, Exeter , 3 Devon Primary Care Trust, Topsham Surgery, Exeter EX3 0EN

Correspondence to: B Vaidya, bijay.vaidya@pms.ac.uk

doi:10.1136/bmj.b2384

The first 150 words of the full text of this article appear below.


A 34 year old woman presented with a 12 month history of increasing tiredness, anorexia, weight loss, and depression. During that period, she had tried two different antidepressant tablets without benefit. She saw her general practitioner’s locum, who thought she looked tanned. Her blood pressure was 90/60 mm Hg, although it had always tended to be low. Her serum sodium concentration was 130 (normal range 135-145) mmol/l and potassium concentration was 5.7 (normal range 3.5-5.5) mmol/l. A short Synacthen (tetracosactide) test showed an inadequate serum cortisol response, which together with raised plasma adrenocorticotrophic hormone confirmed the diagnosis of Addison’s disease.


Addison’s disease (also known as primary adrenal insufficiency) is a chronic disorder of the adrenal cortex resulting in inadequate secretion of glucocorticoid and mineralocorticoid. The commonest cause of Addison’s disease in developed countries is autoimmune disorder and in developing countries is tuberculosis.1




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