Adrenal disorders Flashcards

1
Q

name a condition that affects the production of each of the adrenal hormones.

A
aldosterone - Conn's 
cortisol - cushings (hyperfunction)
cortisol - addisons (hypofunction)
sex hormones - congenital adrenal hyperplasia 
epinephrine - phaeochromocytoma
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2
Q

what is the cause of Conn’s syndrome?

A

over production of aldosterone caused by a tumour of the pituitary gland

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3
Q

what is the presentation of a paeochromocytoma?

A

episodic / paroxysmal attacks;

  • palpitations
  • sweating
  • pallor
  • headache
  • tremor
  • anxiety / fear
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4
Q

what is the most common cause of addison’s disease?

A

autoimmune destruction of the adrenal glands

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5
Q

what is the presentation of Addison’s disease?

A
fatigue
weakness
anorexia / weight loss
salt craving 
unexplained vomiting or diarrhoea 
postural symptoms
hypotension 
skin pigmentation / vitiligo
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6
Q

what is commonly associated with Addisons disease?

A

other autoimmune conditions because if you have one your are likely to have another such as;

  • type 1 diabetes
  • thyroid disease (hashimotos)
  • premature ovarian failure
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7
Q

when carrying out a random cortisol if there is suspicion of addisons disease, what values would suggest addisons or not?

A

> 700 nmol/L = not addisons

< 700 nmol/L (adrenal status still uncertain but may be addisons)

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8
Q

what is the name of the confirmatory test for diagnosing addisons?

A

Synacthen test

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9
Q

what is the treatment for addisons?

A

hydrocortisone therapy 20-30mg
- given in divided dose i.e. 20mg in the morning and 10mg at dinner time

prednisolone 7.5mg
dexamethasone 0.75mg
mineralocorticoid therapy - flurocortisone 50-300mg (resolve the hypotension & hyponatraemia)

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10
Q

why can addison’s cause hypotension and salt cravings?

A

with cortisol insufficiency from the hypofunctioning adrenal gland , it can also cause hypo secretion of mineralocorticoids - aldosterone

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11
Q

what are the causes of cushings syndrome?

A

pituitary tumour
actopic ACTH secretion from lung carcinoma
adrenal tumour
corticosteroid therapy

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12
Q

what is the presentation of cushings syndrome?

A
central obesity
muscle atrophy 
proximal weakness
pink striae 
moon face 
hypertension
hyperglycaemia - diabetes mellitus
poor wound healing 
osteoporosis 
hirsutism 
amenorrhoea / galactorrhoea 
acne 
personality changes / depression
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13
Q

how would you screen for curhsings syndrome?

A

24 hour urine free cortisol

1mg overnight dexamethasone test

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14
Q

what results in the tests of low dose and high dose dexamthasone would be suggestive of cushings disease (tumour in the pituitary)?

A

with a low dose dexamthasone the cortisol levels are still high - doesnt respond
but it responds to high levels as the cortisol levels will derease

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15
Q

what is the plasma renin activity (PRA) and plasma aldosterone concentration (PAC) like in someone with conn’s syndrome?

A

plasma renin decreased

plasma aldosterone raised

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16
Q

if there is increased plasma renin activity and increased plasma aldosterone concentration, what would you investigate next to come to a diagnosis?

A

increased PRA & PAC = secondary hyperaldosteronism

investigate for causes such as renovascular hypertension, coarctation of aorta, diuretic use, malignant hypertension etc
(causes of secondary hypertension that isnt caused by an endocrine condition)

17
Q

what could be the cause of a decreased plasma renin activity and a decreased plasma aldosterone concentraion?

A

congenital adrenal hyperplasia

18
Q

what tests would you carry out to establish the source of the over production of aldosterone ? (after PRA and PAC has been carried out)

A

CT scan of adrenal glands
upright posture test
adrenal venous sampling
24 hour urine aldosterone and sodium

19
Q

why is a phaeochromocytoma termed as the 10% tumour?

A
10% malignancy
10% extra adrenal
10% multiple
10% hyperpglycaemia 
but 30% has an inherited origin
20
Q

what are the first 2 tests you carry out if your suspect adrenal insufficiency?

A
plasma cortisol ( < 700nmol/L)
synACTHen test ( < 500 mmol/L)
21
Q

how do you differentiate whether the low cortisol is due to primary adrenal insufficiency or secondary?

A

plasma ACTH levels
low ACTH = secondary
high ACTH = primary

22
Q

what tests would you carry out to investigate the cause of primary adrenal insufficiency?

A

MRI adrenal glands - tumour, infarction, haemorrhage, infection
serum antibodies- Addison’s, anti 21 hydroxylase, other autoimmune conditions
screen for rarer causes such as HIV, TB, secondary malignancy

23
Q

how long is a patient on steroid therapy for it to suppress their pituitary adrenal axis?

A

> 7.5mg prednisolone daily for 3 weeks

24
Q

what adjustments do people on steroid therapy (due to adrenal insufficiency) have to make if they have vomiting/diarrhoea?

A

IM injection of hydrocortisone

not allowed to do it themselves

25
Q

what adjustments do patients on steroid therapy (due to adrenal insufficiency) have to make if they get the flu / minor illness?

A

double their dose of steroids

26
Q

what can be the cause of adrenal insufficnecy in women if its not addisons?

A

adrenal infiltration, infarction, haemorrhage or infection

27
Q

what can be the cause of adrenal insufficiency in males if its not addisons?

A

adrenal infiltration, infarction, haemorrhage, or infection

adrenoleucodystrophy

28
Q

what does the presence of very long chain fatty acids (VLCFA) in males with adrenal insuficiency indicate?

A

adrenoleukodystrophy

29
Q

what are the rare causes of addison’s disease?

A
malignancy i.e. breast, melanoma, lung
infiltration
infection i.e. TB, HIV
infarction
iatrogenic
21 hydroxyls insufficiency