Acromegaly Flashcards

1
Q

excess of what? where is this usually secreted?

A

growth hormone. secreted from pituitary

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2
Q

usually caused by what pathology

A

GH secreting pituitary adenoma. usually macro

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3
Q

ix acromegaly

A

insulin growth factor (initial screen)
glucose tolerance test
NB random GH not done because can get it wrong

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4
Q

what is shown in glucose tolerance test and why

A

no decrease in GH, (GH secretion is normally suppressed with increased glucose))

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5
Q

what happens to insulin growth factor 1

A

increases (GH stimulates IGF-1 production)

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6
Q

why is MRI done

A

look for pituitary adenoma

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7
Q

complications of acromegaly

A

HF
CHD
hypertension
neoplasia

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8
Q

onset

A

slow. diagnosis is usually 4-7 years after onset of excessive GH secretion

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9
Q

male of female more

A

equally affected

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10
Q

presentation

A
  • headaches (due to mass)
  • visual field defect
  • increase in ring/shoe size
  • macroglossia (large tongue)
  • large jaw
  • coarsening of facial features
  • frontal bossing
  • excessive sweating common
  • mild hirsitism
  • T2DM
  • osteoarthritis
  • carpal tunnel
  • hypertension
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11
Q

commonest visual field defect

A

bitemporal hemianopia

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12
Q

what may also be secreted by the tumour

A

prolactin -> galactorrhoea and amenorrhoea

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13
Q

increased risk of what cancers

A

colon, thyroid

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14
Q

rx

A

trans sphenoidal surgery first line. radiotherapy if refractory
med options if not suitable for surgery: somatostain analogues (octreotide), dopamine agonists (bromocriptine, cabergoline)

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