6 normal pituitary function and disease Flashcards

1
Q

what happens to prolactin levels if pituitary stalk is damaged and why?

A

increase in prolactin levels- loss of communication with hypothalamus and anterior pituitary

prolactin’s principle control is inhibitory

TRH has stimultatory role

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2
Q

what is the most common cause of pituitary disease?

A

pituitary tumour

10% of all intracranial neoplasm

Mostly benign, slow-growing (years) adenomas

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3
Q

define adenoma

macroadenoma

microadenoma

A

benign tumours of epithelial tissue of glangular origin

>10mm diameter

<10mm diameter

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4
Q

how can adenomas cause problems?

A
  • Over-production of a pituitary hormone
  • Inadequate production of other hormones- pituitary gland cells push against edges of bony compartment
  • Local effects on anatomically-related structures (visual disturbances, headaches- increase in intracranial pressure)
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5
Q

prevelance of tumours

what proportion are endocrine active tumours?

what is the main type (40-50%)?

A

3/4 are endocrine active tumours

Prolactinoma (40-45%) hyperprolactinaemia

GH-secreting (20%) acromegaly (adults), gigantism (children)

ACTH-secreting (10-15%) Cushing’s disease

LH/ FSH-secreting: rare

TSH-secreting: rare

Non-functioning (20-25%) mechanical symptoms- headaches, facial disturbances (non-secreting) hypopituitarism – low levels of hormones: most likely consisting of chromophobes

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6
Q

investigations of pituitary tumour

A
  1. signs and symptoms
  2. endocrine investigation: baseline hormone levels

dynamic tests:

stimulation- if hyposecretion suspected

suppression- if hypersecretion suspected

  1. imaging: CT or MRI
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7
Q

example of stimulation test:

A

secondary hypothyroidism

Inject more TRH (hypothalamus), normally stimulate TSH (ant pituitary). Failure to stimulate TSH/ T4 suggests deficiency of TSH. (lack of response to exogenous TRH)

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8
Q

example of suppression test:

A

acromegaly (GH tumour)

Oral glucose tolerance test – high plasma [glucose] normally suppress GH release. Failure to lower GH secretion suggests GH tumour.

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9
Q

management of pituitary disease due to tumour:

A
  • Pharmacological management
  • Surgery- preferred method
  • Radiotherapy
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10
Q

what are two types of surgery for pituitary tumour?

which is more common?

A
  1. Craniotomy - through the skull above the eye.
  2. Trans-sphenoidal - through the nose. Most common. Less invasive, patients in hospital less time, better recovery time
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11
Q

hyperprolactinaemia:

  • most common causes
  • symptoms
  • treatment
A
  • Most common cause is prolactinoma. (adenoma secreting pro lactin)
  • Another is damage to the pituitary stalk (dopamine)
  • Symptoms: loss of fertility/ libido, galactorrhoea- milky discharge from breast tissue
  • high [prolactin] inhibit GnRH release
  • Gynaecomastia m>f benign glandular tissue of breast tissue
  • Treatment: mainly with dopamine receptor agonists (e.g. cabergoline, bromocriptine) which inhibit prolactin secretion and shrink tumour.
  • Surgery / radiotherapy considered with tumours resistant to drug therapy.
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12
Q

acromegaly

  • what is it?
  • what is the term that happens in childhood?
  • common cause
  • treatment
  • symptoms
  • who could detect early acromegaly?
A
  • Excessive growth hormone secretion in adulthood

(Excessive GH secretion in childhood leads to extremely tall stature (gigantism))

  • Most common cause is GH-secreting tumour
  • Treatment: principally surgical removal of tumour, radiotherapy in some patients.
    • Somatostatin analogues (e.g. octreotide, lanreotide) inhibit GH release.
    • Bromocriptine (dopamine receptor agonist). Some GH-adenomas have expression of dopamine receptors, which when activated inhibit GH release.
  • coarsening of facial features (look older than their age)
  • enlarged hands and feet
  • headaches, vision disturbance
  • sleep apnoea, general tiredness
  • hypertension, cardiomegaly
  • glucose intolerance (diabetes)
  • irregular or loss of periods (females); impotence (males)
  • As lower jaw enlarges, gaps appear between teeth

Acromegaly may be detected early by dentists

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13
Q

hypopituirarism

define pan- hypopituitarism

  • what is it usually caused by

treatment

A

deficiency of one or more pituitary hormones

Pan-hypopituitarism = deficiency of all pituitary hormones

  • Usually caused by pituitary adenoma, surgery/ radiotherapy of the pituitary.
  • Severe head trauma can damage pituitary stalk.

treatment: hormone replacement

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14
Q

what are potential side effects of surgery and radiotherapy of a pituitary tumour?

A

hypopituitarism and damage to optic pathways

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15
Q

what is Cushing’s syndrome?

what can cause it?

what is the main cause?

treatment

A

excess glucocorticoid activity

caused endogenously and exdogenous (steroid meds)

main cause: endogenous- ACTH secreting anterior pituitary tumour

treatment: remove tumour (radiotherapy too)

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