endocrine disorders Flashcards

1
Q

adrenal steroids

A

adrenal steroids:

mineralocorticoids
glucocorticoids
adrenal androgens

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2
Q

adrenal steroids

A

adrenal steroids:

mineralocorticoids
glucocorticoids
adrenal androgens

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3
Q

disorders of adrenocortical function

A

adrenal hyperfunction:

  • excess cortisol = cushings syndrome
  • excess aldosterone = Conn’s syndrome

adrenal insufficiency:

  • hypocortisolism
  • lack of aldosterone and cortisol
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4
Q

describe adrenocortical excess

A

aldosterone excess:
- conn’s syndrome (primary hyperaldosteronism)

cortisol excess:
- Cushing’s syndrome (may be primary or secondary)

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5
Q

describe control of aldosterone secretion

A

activated by:
RAAS and increased plasma

RAAS is activated by:

  1. reduced renal perfusion
  2. increased sympathetic activity

both interpreted as a fall in blood volume

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6
Q

plasma aldosterone/renin ratio is useful in diagnosis of primary hyperaldosteronism

A

source of excess aldosterone is adrenal

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7
Q

what’s the most common cause of Cushing’s syndrome

A

iatrogenic

  • exogenous glucocorticoids activate cortisol receptor
  • at high doses will shut down HPA
  • adrenal cortex atrophies with lack of ACTH stimulation
  • several days may be required for adrenal to become responsiveness to ACTH again
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8
Q

what is Cushing;s disease due to

A

ACTH secreting pituitary adenoma.

Cushing’s syndrome may also be due to ectopic ACTH source

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9
Q

describe adrenal insufficiency

A

primary:

  • addison’s disease
  • insufficient cortisol and aldosterone

secondary:

  • pituitary or hypothalamic disease
  • insufficient cortisol
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10
Q

describe clinical features of Addison’s

A

primary adrenal insufficiency:

  • hypotension
  • plasma: normal to low
  • plasma: normal to high
  • High ACTH
  • elevated plasma renin

may be unmasked by significant stress or illness
shock, hypotension, volume depletion

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11
Q

Addison’s disease 2

A

progressive, can lead to adrenal crisis = fatal if not treated

hallmark is high ACTH, low cortisol

dynamic test can aid diagnosis: assess ability of adrenal to produce cortisol in response to ACTH

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12
Q

describe ACTH stimulation test

A
  • assess ability of adrenal to produce cortisol in response to ACTH

Short synacthen test
Measure baseline cortisol (9am) and 30 min after 250 µg synacthen (synthetic ACTH) i.m.
Adrenal insufficiency is excluded by an increase in cortisol of >200 nmol/L and/or a 30 min value >550
Long synacthen test
Adrenal cortex ‘shuts down’ in absence of stimulation by ACTH – time needed to regain responsiveness
3-day stimulation with synacthen
In secondary (but not primary) adrenal insufficiency cortisol increases by >200 nmol/L over baseline
Long test not often necessary since ACTH assay can distinguish

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13
Q

disorders of adrenocortical function

A

adrenal hyperfunction:

  • excess cortisol = cushings syndrome
  • excess aldosterone = Conn’s syndrome

adrenal insufficiency:

  • hypocortisolism
  • lack of aldosterone and cortisol
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14
Q

describe adrenocortical excess

A

aldosterone excess:
- conn’s syndrome (primary hyperaldosteronism)

cortisol excess:
- Cushing’s syndrome (may be primary or secondary)

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15
Q

describe control of aldosterone secretion

A

activated by:
RAAS and increased plasma

RAAS is activated by:

  1. reduced renal perfusion
  2. increased sympathetic activity

both interpreted as a fall in blood volume

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

plasma aldosterone/renin ratio is useful in diagnosis of primary hyperaldosteronism

A

source of excess aldosterone is adrenal

17
Q

what’s the most common cause of Cushing’s syndrome

A

iatrogenic

  • exogenous glucocorticoids activate cortisol receptor
  • at high doses will shut down HPA
  • adrenal cortex atrophies with lack of ACTH stimulation
  • several days may be required for adrenal to become responsiveness to ACTH again
18
Q

what is Cushing;s disease due to

A

ACTH secreting pituitary adenoma.

Cushing’s syndrome may also be due to ectopic ACTH source

19
Q

describe adrenal insufficiency

A

primary:

  • addison’s disease
  • insufficient cortisol and aldosterone

secondary:

  • pituitary or hypothalamic disease
  • insufficient cortisol
20
Q

describe clinical features of Addison’s

A

primary adrenal insufficiency:

  • hypotension
  • plasma: normal to low
  • plasma: normal to high
  • High ACTH
  • elevated plasma renin

may be unmasked by significant stress or illness
shock, hypotension, volume depletion

21
Q

Addison’s disease 2

A

progressive, can lead to adrenal crisis = fatal if not treated

hallmark is high ACTH, low cortisol

dynamic test can aid diagnosis: assess ability of adrenal to produce cortisol in response to ACTH

22
Q

describe ACTH stimulation test

A
  • assess ability of adrenal to produce cortisol in response to ACTH

Short synacthen test
Measure baseline cortisol (9am) and 30 min after 250 µg synacthen (synthetic ACTH) i.m.
Adrenal insufficiency is excluded by an increase in cortisol of >200 nmol/L and/or a 30 min value >550
Long synacthen test
Adrenal cortex ‘shuts down’ in absence of stimulation by ACTH – time needed to regain responsiveness
3-day stimulation with synacthen
In secondary (but not primary) adrenal insufficiency cortisol increases by >200 nmol/L over baseline
Long test not often necessary since ACTH assay can distinguish