Endo II - Adrenal Disorders Flashcards
what hormones are produced in the:
zona gomerulosa
zona fasicularis
zona reticularis
adrenal medulla
G - mineralocorticoids
F - glucocorticoids
R - androgens
M - catecholamines
moon face
striae
depression
HTN
DM
hyperpigmentation
menstural abnormalities
Cushing disease
increased ACTH from pituitary
exogenous cushing syndrome - what results in adrenal glands
bilateral adrenal atrophy
cushing disease - pituitary tumour
bilateral adrenal hyperplasia
primary hypecortisolism
atrophy contralateral adrenal gland
ectopic ACTH production
bilateral adrenal hyperplasia
tests for hypercortisolism
urine cortisol
dexamethasone suppression test
plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH increased
pituitary cause - cushing syndrome
plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH decreased
adrenal cause - cushing syndrome
plasma cortisol increased
urine free cortisol increased
LD DST not suppressed
HD DST suppressed
plasma ACTH increased+
triad of hypertension, hypokalaemia, metabolic alkalosis
hyperaldosteronism
hyperaldosteronism:
low renin
high aldosterone
= 1’ or 2’
primary hyperaldosteronism (Conn syndrome)
hyperaldosteronism:
high renin
high aldosterone
= 1’ or 2’
secondary hyperaldosteronism
extra adrenal cause
kidney responds to hyperaldosteronism via aldosterone escape - excretes sodium in urine. It presents as:
hypertension without oedema / hypernatremia
Na+ - high
K+ - low
HCO3 - high
Exaggerated features male & women
Hairiness face / body
Baldness
Acne
Deeper voice
Muscularity
Hirsutism / virilisation in females
androgen excess
what enzyme defects occur in congenital adrenal hyperplasia
17B-hydroxylase
21B-hydroxylase
11B-hydroxylase
enzyme deficiency:
increased aldosterone
increased DOC
increased cortisol
decreased androgen
17B-hydroxylase
increased androgens
decreased cortisol
decreased aldosterone
decreased DOC
21B-hydroxylase
1increased androgens
increased DOC
decreased cortisol
decreased aldosterone
11B-hydroxylase
infant/child
failure to thrive
aldosteron & cortisol deficiency
increased androgens
hyponatremia
hyperkalaemia
serum 17 Oh progesterone test - >1500ng/mL
21 hydroxylase deficiency
classic - salt loosing
Infants/child
Simple virilization
Increase androgens
Only Cortisol deficiency
Early growth of pubic
and axillary hair
serum 17 Oh progesterone test - >1500ng/mL
21 hydroxylase deficiency
classic - non-salt loosing
Adolescence
Typical genitalia
Primary menorrhea
Acne
Hirsutism
Polycystic ovaries
Serum 17 OH progesterone test - >200 ng/mL
21 hydroxylase deficiency
non-classic
17 hydroxyprogesterone - elevated
ACTH - elevated
coristol, androgen, oestrogen - low
17 alpha hydroxylase deficiency
11 droxycorticosterone - high
ACTH - absent/low
renin - low
11B-hydroxylase deficiency