Adrenal Disease Flashcards

(63 cards)

1
Q

what does the adrenal medulla secrete?

A

catecholamines

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2
Q

name two catecholamines

A

noradrenaline

adrenaline

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3
Q

name two adrenal androgens

A

DHEA

androstenedione

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4
Q

what is the starting point for steroid hormones produced by the adrenal glands?

A

cholesterol

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5
Q

what regulates production of aldosterone?

A

RAAS

plasma potassium

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6
Q

what are the three main clinical uses for corticosteroids?

A

suppress inflammation
suppress the immune system
replacement treatment

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7
Q

what are the three routes of administration of corticosteroids?

A

oral
IM
IV

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8
Q

what is adrenal insufficiency?

A

when there is inadequate adrenocortical function

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9
Q

what are the two types of adrenal insufficiency?

A

primary

secondary

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10
Q

what causes primary adrenal insufficiency?

A

disorders of the adrenal gland

addison’s. CAH, adrenal TB/malignancy

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11
Q

what causes secondary adrenal insufficiency?

A

lack of ACTH production

steroids, pituitary disease, hypothalamic disease

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12
Q

what is addison’s disease?

A

autoimmune destruction of the adrenal cortex

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13
Q

how does addison’s present? (5)

A
anorexia
fatigue 
dizziness 
abdominal pain 
skin pigmentation
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14
Q

what is the most common cause of primary adrenal insufficiency?

A

addison’s disease

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15
Q

what biochemistry should raise suspicion of adrenal insufficiency?

A

low sodium
high potassium
hypoglycaemia

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16
Q

what is the diagnostic test for adrenal insufficiency?

A

short synacthen test

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17
Q

what does a short synacthen test involve?

A

measure plasma cortisol before and then 30 mins after an ACTH injection

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18
Q

what is a normal result from a short synacthen test?

A

baseline >250

post ACTH >550

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19
Q

what are ACTH levels like in addison’s disease?

A

raised

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20
Q

what causes the skin pigmentation in addison’s disease?

A

raised ACTH

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21
Q

what are renin and aldosterone levels like in addison’s disease?

A

increased renin

reduced aldosterone

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22
Q

what is the management of primary adrenal insufficiency?

A

hydrocortisone

fludrocortisone

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23
Q

what is cushing’s syndrome?

A

excess cortisol secretion

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24
Q

what group is cushing’s syndrome more common in ?

A

women aged 20-40

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25
name five clinical features of cushing's syndrome
``` bruising striae obesity thin skin proximal myopathy ```
26
what are the three categories of causes of cushing's syndrome?
ACTH dependent ACTH independent iatrogenic
27
name two ACTH dependent causes of cushing's syndrome
cushing's disease | ectopic ACTH/CRH
28
what is cushing's disease?
a pituitary adenoma secreting excess ACTH
29
what is the gold standard test for cushing's syndrome?
low dose dexamethasone suppression test
30
what happens in a low dose dexamethasone suppression test?
patient takes 0.5mg of dexamethasone every 6 hours for 48 hours
31
what is a normal result for a low dose dexamethasone suppression test?
cortisol suppressed to less than 50 at the end of the test
32
what is the most common cause of cushing's syndrome?
iatrogenic - due to prolonged steroid therapy
33
what is primary aldosteronism?
autonomous production of aldosterone
34
what is the most common cause of secondary hypertension?
primary aldosteronism
35
what are the three main clinical features of primary aldosteronism?
hypertension hypokalaemia alkalosis
36
what are the two main causes of primary aldosteronism?
adrenal adenoma | bilateral adrenal hyperplasia
37
what is an adrenal adenoma causing primary aldosteronism called?
conn's syndrome
38
how is primary aldosteronism diagnosed?
confirm aldosterone excess | confirm cause
39
how is aldosterone excess confirmed in primary aldosteronism?
measure the aldosterone:renin saline suppression test = failure to suppress by >50% = PA
40
how is conn's syndrome cured?
surgical removal
41
how is bilateral adrenal hyperplasia causing primary aldosteronism treated?
mineralocorticoid antagonists (spironolactone or eplerenone)
42
what causes congenital adrenal hyperplasia?
deficiency in an enzyme needed for cortisol synthesis
43
what is the most common cause of congenital adrenal hyperplasia?
21a-hydroxylase deficiency
44
how is congenital adrenal hyperplasia inherited?
autosomal recessive pattern
45
what does a 21a-hydroxylase deficiency result in?
blocks production of cortisol and aldosterone increased androgens
46
what are the two types of congenital adrenal hyperplasia?
classic | non classic
47
when does classic congenital adrenal hyperplasia present?
infancy
48
how can classic congenital adrenal hyperplasia present?
adrenal crisis or adrenal insufficiency virilization
49
what causes non classic congenital adrenal hyperplasia?
partial 21a-hydroxylase deficiency
50
when does non classic congenital adrenal hyperplasia present?
adolescence/adulthood
51
how does non classic congenital adrenal hyperplasia?
hirsutism menstrual issues infertility
52
how is congenital adrenal hyperplasia diagnosed?
measure 17-OH progesterone
53
how is congenital adrenal hyperplasia managed?
steroid replacement
54
what are catecholamines derived from?
tyrosine
55
where are catecholamines secreted?
adrenal medulla
56
how does pheochromocytoma present?
hypertension postural hypotension paroxysmal sweating, headache, pallor and tachycardia can be asymptomatic
57
what is a pheochromocytoma called if it is extra adrenal?
paraganglionoma these are found in the sympathetic chain
58
how can pheochromocytoma be fatal?
arrythmia | ischaemia
59
how is pheochromocytoma diagnosed?
urine or plasma catecholamine measurement | MRI
60
what is done prior to surgery for pheochromocytoma?
alpha blockade followed by beta blockade
61
what alpha blocker is given prior to pheochromocytoma surgery?
phenoxybenzamine
62
what beta blocker is given prior to pheochromocytoma surgery?
propranalol, atenolol or metoprolol
63
what is the treatment of choice for pheochromocytoma?
laparoscopic surgical excision