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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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