Hypothalamus / pituitary tutorial notes Flashcards

1
Q

what do disorders relating to the hypothalamus / pituitary usually present with?

A
  • symptoms of excess or deficiency with one or more of the hormones they produce
  • other symptoms may be neurological - eg headache or visual disturbances (remember optic chiasm)
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2
Q

what are the 5 main causes of hypothalamic/pituitary disorders?

the 5 I’s

A
  • idiopathic - ie no cause
  • invasion - ie tumour
  • Infarction - death of tissue
  • Iatrogenic - caused by surgery, drugs etc
  • Injury - ie head trauma
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3
Q

what is sheehans syndrome and what symptoms can it cause?

A
  • a condition resulting from damage to the pituitary gland due to low levels of oxygen (by blood loss) during child birth
  • can cause difficulty in breast feeding and failure to menstruate after delivery
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4
Q

what are the 3 main types of investigations that can be done in order to diagnose someone?

A
  • basal blood tests
  • dynamic tests
  • imaging
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5
Q

if a hormone is stimulated but levels do not rise, what might be the problem?

A

a problem in the production of the hormone

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6
Q

if an inhibiting substance is given, but normal negative feedback does not occur, what is likely to be the problem?

A

it is likely that there is a hormone - producing tumour causing the symptoms

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7
Q

what are the 3 main forms of treatment?

A
  1. replacement hormones - for defiency problems
  2. surgery or radiotherapy - for tumours
  3. drugs that inhibit production - ie when surgery isnt suitable
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8
Q

what is agromegaly?

A

caused by hypersecretion of GH in adults, usually due to a pituitary tumour

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9
Q

in children, what is agromegaly normally referred to as?

A

gigantism

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10
Q

what are the main clinical symptoms of agromegaly?

A
  • enlarged hands and feet
  • enlarged skull circumference
  • enlarged liver, kidneys and heart
  • large lower jaw, nose and tongue
  • spacing between the lower teeth
  • loss of peripheral vision (compression of the optic chiasm)
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11
Q

what are the main clinical signs of agromegaly?

A
  • 1 in 3 have hypertension
  • 1 in 10 are hypercalcaemic (high Ca2+)
  • 1 in 4 are glucose intolerant
  • altered bone structure
  • 1 in 5 have hyperthyroidism
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12
Q

what is an OGTT test?

A

an oral glucose tolerance test

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13
Q

what does an OGTT test involve?

A
  • glucose is administered and insulin release is stimulated
  • hyperglycemia SHOULD (as a result of glucose administeration) supresses GH secretion
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14
Q

in the case of an individual with suspected agromegaly, what will happen in the OGTT test?

A
  • hyperglyceamia should suppress GH secretion, however if there is no supression or if GH levels continue to rise - this indicates agromegaly
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15
Q

what is an insulin tolerance test & what can it be used to diagnose?

A
  • test that measures the response of the pituitary, adrenal, and insulin receptors to a hypoglycemic episode induced by insulin injection
  • it can be used to diagnose diabetes, neuroendocrine tumours, and insulin resistance
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16
Q

what effect does hypoglycemia normally have on GH secretion?

hypoglycemia - low glucose levels

A
  • normally stimulates the release of GH and GH levels should then return to normal as blood glucose levels recover their normal level
17
Q

what might be suspected if the baseline GH levels are elevated during an insulin tolerabce test?

A
  • ie if the baseline GH levels are elevated - atypical response
  • GH continues to increase even when blood glucose levels are normalised - this isnt normal
18
Q

what is octreotide?

A

a somatostatin analogue - which will inhibit GH secretion

19
Q

what is the most common symptoms of sheehans syndrome?

A
  • absence of lactation - agalactorrhea
  • loss of pituitary gland hormone production - hot flushes, decreased sex drive
  • symptoms of hypothyroidism - low T3 and T4 and low TSH - fatigue, bradycardia, hypotension
  • adrenal insufficney may also occur - fatigue and weight loss
20
Q

what can occur and is a rare manifestation of sheehans syndrome?

A

diabetes insipidus

21
Q

in a blood test of a patient suspected with sheehans syndrome, what is to be expected with the levels of anterior pituitary hormones?

A

there will be a low basal hormone level

22
Q

what is the treatment for sheehans syndrome?

A
  • life long replacement of deficient hormones
  • hypothyroidims treted with levothryoxine
  • cortisol deficiency treated with prednisone or hydrocortisone
  • gonadotropin deficiency can be treated with estrogen and progesterone