Adrenal Gland physiology and disease Flashcards

1
Q

what are some of the common symptoms and signs of Addison’s disease?

A
  • tiredness
  • weight loss
  • skin pigmentation/vitiligo
  • hypotension
  • vomiting/diarrhoea
  • hypoglycaemia
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2
Q

is Addison’s disease hypoactivity or hyperactivity of the adrenal gland?

A

hypoactivity

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3
Q

which endocrine gland is affected in Addison’s disease?

A

adrenal gland

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4
Q

what tests should be done to diagnose Addison’s disease?

A
  • routine blood tests (incl U&E, FBC, glucose)
  • random cortisol sample
  • short Synachten test
  • serology for anti 21-hydroxylase antibodies
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5
Q

what are some clues to a possibility of Addison’s disease?

A
  • unexplained hypoglycaemia
  • previous weight loss or depression
  • mismatch between disease severity and symptoms
  • other endocrine problems
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6
Q

how is Addison’s disease managed?

A
  • with glucocorticoid and mineralocorticoid replacement
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7
Q

what drugs are used to replace low cortisol levels in Addison’s disease?

A
  • hydrocortisone
  • prednisolone
  • dexamethasone
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8
Q

what drugs are used to replace low aldosterone levels in Addison’s disease?

A
  • fludrocortisone
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9
Q

what should you do in case of severe illness (eg Addisonian crisis)?

A
  • IV hydrocortisone 100mg
  • 50-100mg IV hydrocortisone every 8 hours
  • once symptoms pass, reduce by half each day until back at the normal replacement levels
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10
Q

what are some of the possible causes of Addison’s disease?

A
  • autoimmune
  • iatrogenic
  • infiltrative
  • inflammation
  • infection
  • infarction
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11
Q

what special care should be taken for Addison’s disease patients when they are unwell for other reasons (eg flu)?

A

double dose of cortisol replacement while they are ill

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12
Q

what should patients with Addison’s disease never do?

A

stop their glucocorticoid replacement suddenly

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13
Q

what are the risks of suddenly stopping glucocorticoid replacement?

A

Addisonian crisis due to atrophy of adrenal gland while patient has been on replacement therapy

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14
Q

which antibodies should be tested for Addison’s disease?

A

anti 21-hydroxylase antibodies

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15
Q

if Addison’s disease is secondary, will the plasma ACTH levels after Synachten test be low or high?

A

low

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16
Q

if Addison’s disease is primary, will plasma ACTH levels after Synachten test be low or high?

A

high

17
Q

what hormones trigger the release of adrenal hormones?

A

CRH from hypothalamus

ACTH from pituitary

18
Q

what class of steroids are secreted in the adrenal glands?

A

cholesterol-derived steroid hormones

19
Q

what are the layers of the adrenal gland called, and what class and type of hormones do they secrete?

A

zona glomerulosa - mineralocorticoids (aldosterone)
zona fasciculata - glucocorticoids (cortisol)
zona reticulata - sex hormones
medulla - catecholamines (adrenaline/noradrenaline)

20
Q

what are the two commonest causes of hyperaldesteronism?

A

bilateral hyperplasia

unilateral adenoma

21
Q

name the main feature found in hyperaldesteronism, and explain why

A

hypertension, because excess of aldosterone causes excess sodium retention, and therefore water retention and increased blood volume

22
Q

what investigations are carried out to diagnose hypercortisolism?

A

dexamethasone suppression test
24hr cortisol urine test
cortisol-ACTH test
imaging

23
Q

what are the main questions to be answered when diagnosing hypercortisolism?

A
  • confirm diagnosis
  • determine if ACTH dependent or independent
  • determine if pituitary related or not
  • localise lesion
24
Q

list possible causes of ACTH-dependent hypercortisolism

A
  • pituitary adenoma

- ACTH secreting tumour elsewhere in body

25
Q

list possible causes of ACTH-independent hypercortisolism

A
  • adrenal tumour

- steroid medication

26
Q

list some signs of Cushing’s disease

A
moon face
buffalo hump
wasting in arms/legs
central obesity
striae
hirsutism
bruising
27
Q

what is another name for hypercortisolism?

A

cushing’s syndrome

28
Q

what is hyperaldosteronism called, and what are its main features?

A

conn’s syndrome

hypertension and hypokalaemia

29
Q

would you expect cortisol levels to be high or low at night?

A

low

30
Q

explain why a dexamethasone suppression test is done to diagnose cushing’s disease

A

because administration of corticosteroids would normally suppress ACTH and adrenal production of cortisol.
if dexamethasone is not causing suppression of body’s ACTH/cortisol, there is something wrong in the feedback system

31
Q

what test is used to determine which side of a pituitary is affected by an adenoma in cushing’s disease?

A

ACTH tested in blood sample from petrosal sinuses on each side of pituitary

32
Q

what ratio is used to screen for conn’s syndrome?

A

aldosterone/renin ratio
24hr urine aldosterone test
adrenal vein sampling

33
Q

what aldosterone/ratio would be suggestive of conn’s syndrome?

A

> 20

34
Q

what imaging technique is preferred to test for an adrenal mass?

A

abdominal CT scan

35
Q

what is the main cause of congenital adrenal hyperplasia?

A

21 hydroxylase deficiency

36
Q

which hormones depend on 21 hydroxylase?

A

mineralocorticoids (aldosterone)

glucocorticoids (cortisol)