Primary adrenal insufficiency (Addison's disease)
Clinical Features
decreased cortisol, adrenal sex hormone, and aldosterone secretion
S/S - weakness, paresthesias, cramping, N, V, D, intolerance to stress, and personality changes (irritability and restlessness), 'salt-craving'
- 99% weakness
- 97% weight loss
- 34% Abdominal pain
- 20% Anorexia progressing to nausea and vomiting
- 19% Constipation
Chronic cases - small heart, weight loss
- hyperpigmentation of the skin - diffuse brown, tan, or bronze darkening (especially palmar creases) due to increased pituitary secretion of ACTH and melanocyte-stimulating hormone (MSH)
- ACTH is derived from a larger precursor molecule called proopiomelanocortin (POMC). When POMC is cleaved to produce ACTH, other melanocyte-stimulating hormones (MSH) are also produced. These MSHs have the effect of stimulating melanocytes in the skin to produce more melanin, the pigment responsible for skin colour
- primary Addison's is associated with hyperpigmentation whereas secondary adrenal insufficiency is not
- vitiligo
- sparse axillary hair; loss of pubic hair in women
- (arterial) hypotension - orthostatic (secondary to lack of vascular effect of cortisol on vascular tone)
- hypoglycaemia
- hyponatraemia and hyperkalaemia may be seen
- crisis: collapse, shock, pyrexia
Up to half of the patients with autoimmune adrenalitis have other autoimmune disorders, which may also flare up in the postpartum period.
N.B. Tuberculosis (TB) is a common cause of chronic Addison's disease in endemic areas. (most common cause worldwide)