Endocrine

Addison's Disease

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Pathology

Glucocorticoid and mineralocorticoid deficiency due to failure of adrenal glands. .

Aetiology

Autoimmune - 90% of cases 
Infections - TB, HIV 
Congenital - Congenital Adrenal Hyperplasia 
Malignancy – Lymphoma, metastasis
Infiltration - Amyloidosis or sarcoidosis
Vascular – Haemorrhage, infarction, anticoagulants, meningococcal sepsis 
(Waterhouse-Friderichsen Syndrome), antiphospholipid syndrome. 
Iatrogenic – Adrenalectomy
Drugs – Ketoconazole, busulfan, methadone 

Signs

Hyperpigmentation, postural hypotension, muscle wasting, vitiligo .

Symptoms

Fatigue, weight loss, nausea, poor appetite, dizziness
Addisonian Crisis: Fever, vomiting, abdominal pain, hypotension, tachycardia, 
collapse, coma and hypovolaemic shock.

Investigations

Bloods: Hyponatraemia, hyperkalaemia, hypoglycaemia, TFTs, Coeliac screen,
serum cortisol (low), serum ACTH (raised), short synacthen test
Imaging: Chest X-ray, CT adrenals, bone density scan to monitor osteoporosis

Treatment

Hydrocortisone 10-20mg/day in divided doses – should be doubled when ill
Fludrocortisone 0.05-0.2 mg/day
Addisonian Crisis Treatment (5S’s) - Salt (saline), Sugar (Dextrose), Steroids, 
Support, Search for precipitating cause

Prognosis

Life expectancy reduced by 10-20 years. Steroid over-replacement leads to increased morbidity 
Adrenal crisis at presentation/intercurrent illness, steroid over-replacement, other autoimmune conditions 

Key Facts

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Key Images

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Key References

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