Endo Flashcards

1
Q

what are the 3 types of adrenal disease?

A

addisons (primary adrenal insufficiency)

conns syndrome (primary hyperaldosteronism)

phaeochromocytoma

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2
Q

what is conns syndrome?

A

primary hyperaldosteronism - excess aldosterone production by the zone glomerulosa of adrenal gland (produces mineralocorticoids)

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3
Q

what causes conns syndrome?

A

adrenal adenoma

bilateral idiopathic adrenal hyperplasia

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4
Q

how would someone with conns syndrome present?

A
  • hypertension - headaches, flushing
  • hypokalaemia - fatigue, muscle weakness, headaches, parasthesia, constipation, HR rhythm changes
  • alkalosis (metabolic)
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5
Q

describe the RAAS system

A
  • 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)
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6
Q

what is the role of aldosterone?

A
  • 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
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7
Q

what happens to the RAAS system in conns syndrome?

A
  • breakdown in normal negative feedback
  • inappropriately high aldosterone in blood
  • leads to excess Na+ and water reabsorption and vasoconstriction → high BP
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8
Q

how do we investigate someone with suspected conns?

A
  • 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
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9
Q

how do we manage someone with conns syndrome?

A

drugs - K sparing diuretics (ald antagonist) = spironolactone

surgery - laparoscopic adrenalectomy

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10
Q

what is phaeochromocytoma?

A

neuroendocrine tumour of the adrenal medulla

It secretes excessive amounts of catecholamines (adrenaline) and causes high BP

It is a treatable hypertension!

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11
Q

what causes phaeochromocytoma?

A

familial germline mutations - RET, NF1, VHL, SDH genes

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12
Q

how might someone with phaeochromocytoma present?

A

usually asymptomatic

throbbing headache

sweating

palpitations

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13
Q

what happens to the cardiovascular system of someone with phaeochromocytoma?

A

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

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14
Q

what is a hypertensive emergency in a patient with phaeochromocytoma?

A

when BP is >180/120

small vessels start to break in the:

heart -> CHF
brain -> ischaemic or haemorrhagic stroke
eye -> retinal haemorrhage
kidney -> failure

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15
Q

what investigations would you organise for someone with suspected pheochromocytoma?

A

24 hour urine collection (catecholamines and metanephrine)

US and CT scan

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16
Q

how do we manage someone with pheochromocytoma?

A

surgical excision of neuroendocrine tumour