Endo Flashcards
what are the 3 types of adrenal disease?
addisons (primary adrenal insufficiency)
conns syndrome (primary hyperaldosteronism)
phaeochromocytoma
what is conns syndrome?
primary hyperaldosteronism - excess aldosterone production by the zone glomerulosa of adrenal gland (produces mineralocorticoids)
what causes conns syndrome?
adrenal adenoma
bilateral idiopathic adrenal hyperplasia
how would someone with conns syndrome present?
- hypertension - headaches, flushing
- hypokalaemia - fatigue, muscle weakness, headaches, parasthesia, constipation, HR rhythm changes
- alkalosis (metabolic)
describe the RAAS system
- Normally, if there is a drop in BP, reduced blood flow in renal artery stimulates the release of renin from the kidney which aids the conversion of angiotensinogen → angiotensin I which travels to lungs where ACE aids in conversion of ang I → ang II
- ang II stimulates the release of aldosterone from adrenal cortex
- also causes vasoconstriction (increase BP), stimulates ADH release (water reabsorption)
- normal BP and normal flow through renal artery reduces renin secretion and down-regulates RAAS (negative feedback)
what is the role of aldosterone?
- aldosterone effects:
- binds to Na/K pumps
- drives K+ out, drives Na+ in and water follows into blood = increases BP
- stimulates ATPase pumps
- drives H+ (protons) out, bicarb in = increases in pH
- binds to Na/K pumps
what happens to the RAAS system in conns syndrome?
- breakdown in normal negative feedback
- inappropriately high aldosterone in blood
- leads to excess Na+ and water reabsorption and vasoconstriction → high BP
how do we investigate someone with suspected conns?
- plasma aldosterone/renin ratio - high ald, low renin
- high-res CT abdo - differentiate between unilateral and bilateral
- adrenal venous sampling - to find which gland secreting excess
how do we manage someone with conns syndrome?
drugs - K sparing diuretics (ald antagonist) = spironolactone
surgery - laparoscopic adrenalectomy
what is phaeochromocytoma?
neuroendocrine tumour of the adrenal medulla
It secretes excessive amounts of catecholamines (adrenaline) and causes high BP
It is a treatable hypertension!
what causes phaeochromocytoma?
familial germline mutations - RET, NF1, VHL, SDH genes
how might someone with phaeochromocytoma present?
usually asymptomatic
throbbing headache
sweating
palpitations
what happens to the cardiovascular system of someone with phaeochromocytoma?
individual’s adrenal gland (medulla) produces excess catecholamines
these act on smooth muscle causing vasoconstriction
this increases total peripheral resistance
HR and CO also increase leading to hypertension
what is a hypertensive emergency in a patient with phaeochromocytoma?
when BP is >180/120
small vessels start to break in the:
heart -> CHF
brain -> ischaemic or haemorrhagic stroke
eye -> retinal haemorrhage
kidney -> failure
what investigations would you organise for someone with suspected pheochromocytoma?
24 hour urine collection (catecholamines and metanephrine)
US and CT scan