MEH 16 - Pituitary Disorders Flashcards

1
Q

What are the 2 different ways in which pituitary tumours may present clinically?

A

1) Mass effect of tumour on local structures - tumour can push up on optic chiasm leading to vision loss, or sideways causing painful headaches + double vision.
2) Abnormality in pituitary function - a hypo or hyper-secretion of a hormone.

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2
Q

Which anterior pituitary hormone is the only one under negative/inhibitory control?

A
  • Prolactin, under inhibitory control by dopamine

- Therefore, it is the only hormone that is INCREASED by a pituitary tumour, all others will be decreased.

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3
Q

What are the effects of gonadotropin deficiency (FSH + LH) in children + adults?

A
  • Delayed puberty in children
  • Loss of secondary sexual characteristics in adults
  • Loss of periods early sign in women
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4
Q

What are the effects of TSH + ACTH deficiencies?

Which one is particularly dangerous?

A
  • TSH = low thyroid hormones, cold, weight gain, tiredness, low T4 + non-elevated TSH.
  • ACTH = low cortisol, tired, dizzy, low BP, low sodium. Particularly dangerous + can be life threatening.
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5
Q

What kind of tests would you do if you suspected a hormone deficiency, or a hormone excess?

A

Hormone deficiency = Stimulation test, e.g.: stimulate adrenals w/ACTH if you suspect cortisol deficiency.

Hormone excess = Suppression test, e.g.: suppress ACTH with steroids for cortisol excess.

NB: also can use MRI to image pituitary gland in sagittal/coronal plane.

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6
Q

What is a prolactinoma?
What is the name given to a large/small tumour?
How should prolactinomas be treated?

A
  • A prolactin-secreting pituitary tumour
  • Large tumour (>1cm) = macro-adenoma
  • Small tumour (<1cm) = micro-adenoma
  • Prolactinomas treated with dopamine agonists, as dopamine inhibits prolactin release, NOT an operation, even if tumour is large causing visual problems.
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7
Q

What are the symptoms of hyperprolactinaemia in women?

A
  • Menstrual disturbance
  • Fertility problems
  • Galactorrhea (milky discharge)

This is due to inhibition of LH and FSH due to high PRL levels.

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8
Q

What are the symptoms of hyperprolactinaemia in men?

A
  • Usually present later than women (as no periods)
  • Usually larger tumours (macro-adenomas)
  • Symptoms of low-testosterone are non-specific
  • May present with mass symptoms such as visual loss
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9
Q

What are the signs + causes of acromegaly?

What are the long-term symptoms of untreated acromegaly?

A
  • Large extremities, large hands, feet + protruding jaw, caused by GH-secreting pituitary tumour.
  • Premature CV death, increased risk of colonic tumours, irreversible body changes, hypertension + diabetes.
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10
Q

What biochemical tests would you use to confirm acromegaly?

What are the treatment options for acromegaly?

A
  • Oral glucose tolerance test (OGTT), glucose should suppress GH, if failure to suppress <1 ug/L then diagnosis of acromegaly.
  • Surgical removal of tumour, reduce GH secretion via dopamine agonist or somatostatin analogue or gamma knife radiotherapy.
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11
Q

What is Cushing’s disease?

What are the symptoms?

A
  • An ACTH-secreting pituitary tumour
  • Round pink face, round abdomen, thin skin, easily bruising, red stretch marks (striae) on abdomen, high BP and diabetes.
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12
Q

What is diabetes insipidus?

What is the difference between cranial DI + nephrogenic DI?

A
  • Large quantities of pale (insipid) urine, leading to extreme thirst due to fluid loss.
  • Cranial DI = pituitary disease leading to ADH deficiency
  • Nephrogenic DI = ADH resistance kidney disease
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13
Q

What are the consequences of untreated DI?

A
  • Severe dehydration, hypernatraemia, reduce consciousness coma + death
  • Cranial DI responds well to synthetic ADH (desmopressin)
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14
Q

What is a pituitary apoplexy?

What is the clinical presentation?

A
  • A sudden vascular event in a pituitary tumour (stroke), which can lead to haemorrhage or infarction
  • Sudden onset headache, double vision, cranial nerve palsy, hypopituitarism (cortisol deficiency most dangerous).
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