Endocrine

Acromegaly

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Pathology

Increased growth hormone following puberty after epiphyseal plate closure .

Aetiology

Benign pituitary adenoma (95%), Excess growth hormone releasing hormone, tumours releasing growth hormone.

Signs

Prognathism, frontal bossing, enlarged nose, deep voice, macroglossia, coarse skin texture, enlargement of hands and feet, nerve entrapment, multiple skin tags, goitre

Symptoms

General change in appearance, excess sweating, headaches, visual changes, change in shoe/ring size, joint pains, sleep apnoea, symptoms of diabetes

Investigations

Bloods: Fasting growth hormone and IGF-1 levels, glucose, U&E, lipid profile, 
pituitary profile
Oral Glucose Tolerance Test: No suppression of growth hormone in response 
to glucose load
Imaging: MRI pituitary
ECG:  To assess for cardiac abnormalities
Special Tests: Skin thickness, photographs from the past, cancer screen 

Treatment

Medical: Somatostatin analogues – inhibit growth hormone release, growth 
hormone receptor antagonists or dopamine agonists
Surgical: Trans-sphenoidal surgery 

Prognosis

90% cured by surgery. If left untreated mortality rate is double the rate for the 
general population.
Hypertension, heart failure, carpal tunnel syndrome, sleep apnoea, diabetes osteoarthritis, colonic polyps and cancer

Key Facts

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Key Images

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Key References

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