Adrenal Gland Problems Flashcards

1
Q

what is Addison’s disease?

A

AI destruction of the adrenal cortex

>90% destroyed before symptomatic

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2
Q

what is Addison’s disease associated with?

A

other AI conditions

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3
Q

presentation of Addison’s disease

A
anorexia, weight loss
fatigue
dizziness, low BP
abdominal pain, vomiting, diarrhoea
skin pigmentation (ACTH)- tanned skin without being on holiday
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4
Q

diagnosis of Addison’s disease

A

bloods
short synacthen test
imaging

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5
Q

blood results in Addison’s

A
low Na+, high K+
hypoglycaemia
antibodies
high ACTH
high renin
low aldosterone
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6
Q

what is a short synacthen test?

A

measure cortisol before and after IV/IM ACTH

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7
Q

management of Addison’s disease

A

do not delay for diagnosis
hydrocortisone and fludrocortisone (monitor BP and K+)
educate on sick day rules, never omit, wear identification

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8
Q

why can adrenal crisis occur after long-term steroids?

A

adrenal atrophy

difference is that ACTH and aldosterone are in tact so just give hydrocortisone

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9
Q

what is Cushing’s syndrome?

A

excess cortisol

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10
Q

who is Cushing’s syndrome common in?

A

women 20-40

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11
Q

action of cortisol

A

increases sensitivity to adrenaline allowing the body to cope with stress

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12
Q

presentation of Cushing’s syndrome

A
moon face
proximal weakness
stretch marks
buffalo hump
abdominal fat and striae
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13
Q

diagnosis of Cushing’s syndrome

A

low ACTH, high cortisol (urine, serum, saliva)

dexamethasone suppression test

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14
Q

management of Cushing’s syndrome

A

remove ectopic

bilateral adrenalectomy

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15
Q

what is Conn’s syndrome?

A

excess aldosterone due to adrenal adenoma

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16
Q

presentation of Conn’s

A

significant hypertension
hypokalaemia
alkalosis

17
Q

diagnosis of Conn’s

A

measure aldosterone and renin ratio
saline suppression test
adrenal CT and adrenal vein sampling

18
Q

management of Conn’s syndrome

A

laparoscopic adrenalectomy

if bilateral adrenal hyperplasia use MR antagonists e.g. spironolactone/eplerenone

19
Q

what is congenital adrenal hyperplasia (CAH)?

A

group of conditions caused by enzyme defects in the steroid pathway

20
Q

what is the most common defect in CAH?

A

17-OH

21
Q

two types of CAH

A
  1. classical

2. non-classical

22
Q

presentation of classical CAH

A
males= adrenal insufficiency, poor weight gain
females= genital ambiguity
23
Q

presentation of non-classical CAH

A
hirsute
acne
oligomenorrhoea
precocious puberty
infertility
24
Q

diagnosis of CAH?

A

genetic mutation analysis

basal or stimulated 17-OH progesterone

25
Q

management of CAH in children

A

steroids and aldosterone e.g. spironolactone and eplerenone

surgery

26
Q

management of CAH in adults

A

control androgen excess
restore fertility
steroids

27
Q

spironolactone and eplerenone side effects

A

nausea
rashes
gynaecomastia

28
Q

what is a phaeochromocytoma?

A

tumour of the adrenal medulla that produces excess catecholamines

29
Q

presentation of phaeochromocytoma

A

triad of hypertension, headache and sweating

30
Q

what is a paraganglioma?

A

extra-adrenal tumour found usually in the sympathetic chain

31
Q

diagnosis of phaeochromocytoma

A

catecholamine excess= urine or plasma metanephrines

imaging e.g. CT, MRI, MIBG, PET

32
Q

when should phaeochromocytoma be suspected?

A

FH
resistant hypertension
<50 with hypertension

33
Q

management of phaeochromocytoma

A

alpha and beta blockers (a before b)
fluid and/or blood replacement
surgery and chemo with MIBG if malignant

34
Q

when can catecholamines be raised?

A

CHF
stress

episodic secretion

35
Q

alpha blocker used in phaeochromocytoma?

A

phenoybenzamine