Endo II - Adrenal Disorders Flashcards

1
Q

what hormones are produced in the:
zona gomerulosa
zona fasicularis
zona reticularis
adrenal medulla

A

G - mineralocorticoids
F - glucocorticoids
R - androgens
M - catecholamines

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

moon face
striae
depression
HTN
DM
hyperpigmentation
menstural abnormalities

A

Cushing disease
increased ACTH from pituitary

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

exogenous cushing syndrome - what results in adrenal glands

A

bilateral adrenal atrophy

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

cushing disease - pituitary tumour

A

bilateral adrenal hyperplasia

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

primary hypecortisolism

A

atrophy contralateral adrenal gland

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

ectopic ACTH production

A

bilateral adrenal hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

tests for hypercortisolism

A

urine cortisol
dexamethasone suppression test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH increased

A

pituitary cause - cushing syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH decreased

A

adrenal cause - cushing syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH increased+

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

triad of hypertension, hypokalaemia, metabolic alkalosis

A

hyperaldosteronism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

hyperaldosteronism:
low renin
high aldosterone
= 1’ or 2’

A

primary hyperaldosteronism (Conn syndrome)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

hyperaldosteronism:
high renin
high aldosterone
= 1’ or 2’

A

secondary hyperaldosteronism
extra adrenal cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

kidney responds to hyperaldosteronism via aldosterone escape - excretes sodium in urine. It presents as:

A

hypertension without oedema / hypernatremia
Na+ - high
K+ - low
HCO3 - high

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Exaggerated features male & women
Hairiness face / body
Baldness
Acne
Deeper voice
Muscularity
Hirsutism / virilisation in females

A

androgen excess

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

what enzyme defects occur in congenital adrenal hyperplasia

A

17B-hydroxylase
21B-hydroxylase
11B-hydroxylase

17
Q

enzyme deficiency:
increased aldosterone
increased DOC
increased cortisol
decreased androgen

A

17B-hydroxylase

18
Q

increased androgens
decreased cortisol
decreased aldosterone
decreased DOC

A

21B-hydroxylase

19
Q

1increased androgens
increased DOC
decreased cortisol
decreased aldosterone

A

11B-hydroxylase

20
Q

infant/child
failure to thrive
aldosteron & cortisol deficiency
increased androgens
hyponatremia
hyperkalaemia
serum 17 Oh progesterone test - >1500ng/mL

A

21 hydroxylase deficiency
classic - salt loosing

21
Q

Infants/child
Simple virilization
Increase androgens
Only Cortisol deficiency
Early growth of pubic
and axillary hair
serum 17 Oh progesterone test - >1500ng/mL

A

21 hydroxylase deficiency
classic - non-salt loosing

22
Q

Adolescence
Typical genitalia
Primary menorrhea
Acne
Hirsutism
Polycystic ovaries
Serum 17 OH progesterone test - >200 ng/mL

A

21 hydroxylase deficiency
non-classic

23
Q

17 hydroxyprogesterone - elevated
ACTH - elevated
coristol, androgen, oestrogen - low

A

17 alpha hydroxylase deficiency

24
Q

11 droxycorticosterone - high
ACTH - absent/low
renin - low

A

11B-hydroxylase deficiency

25
name a condition causing 1', 2', 3' adrenocortical insufficiency
1' - waterhouse Friderichsen syndrome 2' pituitary tumour 3' withdrawal glucocorticoids
26
hypoglycaemia hypotension, shock, dizziness skin hyperpigmentation peptic ulcers
hypocortisolism
27
must increase ____ during surgery or vitals drop due to ____ condition
cortisol hypocortisolism
28
decreased Na reabsorption hypotension increased salt craving low BP hyperkalaemia metabolic acidosis
hypoaldosteronism
29
decreased DHEA loss axillary / pubic hair loss libido
hypoandrogenism
30
overnight metyrapone stimulation test in adrenal insufficiency
low 11-deoxycortisol low cortisol high ACTH
31
rapid withdrawal steroids fever vomiting diarrhoea severe abdominal pain high --> low ACTH high cortisol
**adrenal crisis** also occurs following; pituitary apoplexy infection GIT illness hyperthryroidism
32
neisseria meningitidis children acute, bilateral haemorrhagic infarction adrenal cortex fever, neck stiffness, petechial rash, DIC leucocytosis, thomrbocytopaenia low cortisol low aldosterone
Waterhouse-Friderichsen syndrome
33
Cosyntropin test (CST): Negative result = cortisol level stimulation >500-600nmol/L
normal functioning
34
35
AD, Incomplete penetrance Proliferative lesions - hyperplasia & endocrine gland tumours Young Aggressive (more than sporadic) Multiple endocrine organs involved
MENs syndrome
36
Primary hyperparathyroidism Pituitary tumours Enteropancreatic tumours wermer syndrome what is the mutation?
MENIN-1 in MEN-1 syndrome
37
Parathyroid Pheochromocytoma Medulla carcinoma - thyroid Sipple syndrome - what is the mutation?
RET mutation in MEN-2A
38
Pheochromocytoma Medulla carcinoma - thyroid Mucosal neuroma Marfanoid habitus Sipple syndrome - what is the mutation?
RET mutation in MEN-2B