Acromegaly Flashcards

1
Q

Define acromegaly AND gigantism

A

Acromegaly is a condition that is caused by an excess of growth hormone that occurs in adults after fusion of epiphyseal plates

GIGANTIs

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2
Q

Define the epidemiology of acromegaly

A
  • More common in men
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3
Q

Define and explain the causes of acromegaly

A
  1. ) Pituitary adenoma

2. ) Ectopic source: (secondary) a tumour in lung/pancreas that releases excess GHRH or GH itself

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4
Q

Pathology

A

1.) GHRH released from the hypothalamus will stimulate the anterior pituitary to release GH. If an ectopic source is releasing GHRH, this will bypass the axis to stimulate the anterior pituitary to continue releasing GH

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5
Q

What are the signs of acromegaly?

A
  • Acral enlargement: large hands/jaw/nose
  • Frontal bossing: prominent supraorbital ridge
  • Macroglossia
  • Hypertronic heart: HF/hypertension
  • Deep voice
  • Puffy lips
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6
Q

What are the symptoms of acromegaly?

A

1.) Result of tumour growth Bitemporal hemianopia due to compression of the optic nerve, headaches and hypopituitarism

  1. ) Metabolic effects of excess GH:
    - Excessive sweating
    - Acroparaesthesia (tingling/burning sensation in hands and feet)
    - Decreased libido
    - Amenorrhoea
    - Oligomenorrhoea
    - Galactorrhoea
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7
Q

Explain the investigations involved in the diagnosis of acromegaly

A

1.) Measurement of growth hormone

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8
Q

Explain the investigations involved in the diagnosis of acromegaly

A
  1. ) Oral glucose tolerance test: rise in glucose suppress GH. If GH levels are still high then this is acromegaly
  2. ) Serum IGF-1 levels: almost always raised in acromegaly
  3. ) MRI of pituitary fossa: see adenoma

Others

  • visual field test defects
  • ECG + echocardiogram
  • serum prolactin may be raised
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9
Q

Describe the treatment options for acromegaly

A
  1. ) 1st line: Removal of pituitary adenoma producing the GH via trans-sphenoidal approach (complications - hypopituitary, infection, diabetes insipidus)
  2. ) Removal of ectopic source
  3. ) Medication:
    - somatostatin analogues: block GH production + more potent than dopamine agonists] E.g: IM octreotide/lanreotide
    - dopamine agonists: block GH production: ORAL bromocriptine or cabergoline
    - GH agonist e.g. pegvisomant
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