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

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2
Q

moon face
striae
depression
HTN
DM
hyperpigmentation
menstural abnormalities

A

Cushing disease
increased ACTH from pituitary

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3
Q

exogenous cushing syndrome - what results in adrenal glands

A

bilateral adrenal atrophy

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4
Q

cushing disease - pituitary tumour

A

bilateral adrenal hyperplasia

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5
Q

primary hypecortisolism

A

atrophy contralateral adrenal gland

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6
Q

ectopic ACTH production

A

bilateral adrenal hyperplasia

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7
Q

tests for hypercortisolism

A

urine cortisol
dexamethasone suppression test

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8
Q

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

A

pituitary cause - cushing syndrome

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9
Q

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

A

adrenal cause - cushing syndrome

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10
Q

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

A
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11
Q

triad of hypertension, hypokalaemia, metabolic alkalosis

A

hyperaldosteronism

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12
Q

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

A

primary hyperaldosteronism (Conn syndrome)

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13
Q

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

A

secondary hyperaldosteronism
extra adrenal cause

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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

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15
Q

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

A

androgen excess

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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
Q

name a condition causing 1’, 2’, 3’ adrenocortical insufficiency

A

1’ - waterhouse Friderichsen syndrome
2’ pituitary tumour
3’ withdrawal glucocorticoids

26
Q

hypoglycaemia
hypotension, shock, dizziness
skin hyperpigmentation
peptic ulcers

A

hypocortisolism

27
Q

must increase ____ during surgery or vitals drop due to ____ condition

A

cortisol
hypocortisolism

28
Q

decreased Na reabsorption
hypotension
increased salt craving
low BP
hyperkalaemia
metabolic acidosis

A

hypoaldosteronism

29
Q

decreased DHEA
loss axillary / pubic hair
loss libido

A

hypoandrogenism

30
Q

overnight metyrapone stimulation test in adrenal insufficiency

A

low 11-deoxycortisol
low cortisol
high ACTH

31
Q

rapid withdrawal steroids
fever
vomiting
diarrhoea
severe abdominal pain
high –> low ACTH
high cortisol

A

adrenal crisis
also occurs following;
pituitary apoplexy infection
GIT illness
hyperthryroidism

32
Q

neisseria meningitidis
children
acute, bilateral haemorrhagic infarction adrenal cortex
fever, neck stiffness, petechial rash, DIC
leucocytosis, thomrbocytopaenia
low cortisol
low aldosterone

A

Waterhouse-Friderichsen syndrome

33
Q

Cosyntropin test (CST):
Negative result = cortisol level stimulation >500-600nmol/L

A

normal functioning

34
Q
A
35
Q

AD, Incomplete penetrance
Proliferative lesions - hyperplasia & endocrine gland tumours
Young
Aggressive (more than sporadic)
Multiple endocrine organs involved

A

MENs syndrome

36
Q

Primary hyperparathyroidism
Pituitary tumours
Enteropancreatic tumours
wermer syndrome
what is the mutation?

A

MENIN-1
in MEN-1 syndrome

37
Q

Parathyroid
Pheochromocytoma
Medulla carcinoma - thyroid
Sipple syndrome -
what is the mutation?

A

RET mutation
in
MEN-2A

38
Q

Pheochromocytoma
Medulla carcinoma - thyroid
Mucosal neuroma
Marfanoid habitus
Sipple syndrome -
what is the mutation?

A

RET mutation
in
MEN-2B