Pituitary and Hypothalamus Flashcards

1
Q

What is acromegaly?

A

Excess growth hormone

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2
Q

What is the difference between acromegaly and giantisim?

A

Acromegaly if there is excess GH after epiphyseal fusion (adults)
Giantism if there is excess GH before epiphyseal fusion (children)

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3
Q

What causes acromegaly?

A

GH secreting pituitary adenoma

Ectopic tumour

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4
Q

What are the signs + symptoms of acromegaly?

A
Increased height -> giantism
Prominent brow
Increased size and pronouncement of the jaw
Thickened soft tissues
Thickened skin 
Large, sweaty, doughy hands
Snoring/sleep apnoea
Difficulty eating and swallowing
Excessive sweating (at night) and acne
Deeper voice
Interdental separation
Joint pain and proximal muscle weakness
Lethargy
Polydipsia and polyuria
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5
Q

What are the signs + symptoms of acromegaly related to local pituitary adenoma affects?

A

Headaches
Visual field defects
Hyperprolactinaemia (from the same tumour secreting PRL)
Hypopituitarism

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6
Q

What investigations can be done for acromegaly?

A

IGF1 measurement (initial screening test)
Glucose tolerance test (GH unchanged or paradoxically rises, definitive test for diagnosis)
Visual field examination
CT or MRI
Pituitary function tests (have other hormones been impacted)

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7
Q

Why do patients with acromegaly get diabetes?

A

Insulin resistance induced by growth hormone (because it increases plasma glucose levels)

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8
Q

What complications can arise from acromegaly?

A
Diabetes
Hypertension
Heart failure
Carpal tunnel syndrome
Cancer (colonic polyps and colon cancer)
Early CV death
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9
Q

What is 1st line treatment for acromegaly?

A

Transsphenoidal surgery

90% cure rate in microadenoma, 50% in macroadenoma

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10
Q

What medicines can be used for acromegaly treatment?

A

Somatostatin receptor antagonists
Dopamine agonists
GH antagonists

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11
Q

Apart from surgery and medicines what treatment can be offered for acromegaly?

A

Radiotherapy

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