Adrenals Flashcards
Do steroid hormones have a fast or slow response to a stimulus?
Slow - bound to plasma proteins
Functions of AT II
Stimulates aldosterone
Increases water reabsorption
Conn’s syndrome
Hypersecretion of aldosterone due to tumour in glomerulosa
Diagnosis of CAH (bilateral) and Conn’s (unilateral)
Aldosterone:Renin ratio (>750)
Saline suppression test (increased aldosterone)
Treatment of Conn’s and CAH
Conn’s (unilateral): surgery
CAH (bilateral): spironolactone (aldosterone rec antagonist)
Effects of cortisol
Increased lipolysis, decreased glucose uptake, increased gluconeogenesis (liver), increased muscle proteolysis, increased responsiveness to AD = increased CO, decreased Ob activity
Symptoms of cortisol hypersecretion (Cushing’s)
Moonface, cataracts, conjunctival oedema, skin thinning, bruising, purpura, striae, proximal myopathy and muscle wasting, central obesity, buffalo hump (supraclavicular fossae), poor wound healing, muscle weakness, polydipsia, polyuria, depression/euphoria/psychosis
ACTH dependent Cushing’s
Pituitary adenoma = increased ACTH
Headaches, visual field impairment, acne, amenorrhea, frontal balding (high testosterone)
Ectopic ACTH from cancer (small cell)
ACTH independent Cushing’s
Adrenal adenoma/carcinoma, hyperplasia
Low ACTH
Diagnosis of Cushing’s
Low dose dexamethasone suppression test = high cortisol levels
High dose dexamethasone suppression test: high cortisol levels = adrenal/ectopic, low cortisol levels = pituitary
DEXA
Treatment of Cushing’s
Metyrapone
Ketoconazole
Surgery
Effects of adrenaline
Increase HR and force (B1) Vasoconstriction (a1) Vasodilation of skeletal muscle (B2) Decreased insulin secretion (a2) Increased gluconeogenesis and glycogenolysis (a1/B1)
Phaeochromocytoma
Catecholamine secreting tumour of adrenal medulla, arise from sympathetic paraganglia cells (chromaffin cells)
Phaeochromocytoma is associated with which condition?
MEN2 - bilateral, thyroid and parathyroid
NF1
Tuberous sclerosis
Von Hippel Lindau syndrome
Diagnosis of phaeochromocytoma
Urinary catecholamines, CT/MRI/MIBG/PET
Treatment of phaeochromocytoma
Surgery
Alpha (phenoxybenzamine) then Beta blockers (propanolol, atenolol)
Treatment for Addisonian crisis
Glucose
Steroid replacement (IV hydrocortisone, fludrocortisone)
IV fluids
Diagnosis of Addison’s
Short synacthen test (no rise in cortisol)
MRI
Presentation of CAH
Salt losing crisis, ambiguous genitalia, increased androgens, decreased aldosterone, oligomenorrhoea, acne, hirsutism
CAH
21a-hydroxylase deficiency = more testosterone, no cortisol/aldosterone
Auto Recessive
Rate limiting step of steroid production
Cholesterol -> Pregnenolone
How is aldosterone released?
Decreased BP activates RAAS, AT II causes aldosterone release and vasoconstriction
Where are mineralocorticoid receptors?
Kidneys, salivary glands, gut, sweat glands
Treatment for Addison’s
Hydrocortisone and Fludrocortisone
Sick day rules
Symptoms of Addison’s
Anorexia, fatigue, weight loss, dizziness, low BP, abdo pain, N+V, skin pigmentation, decreased Na, increased K, high renin, low aldosterone
Treatment for secondary adrenal insufficiency
Hydrocortisone only
Symptoms of phaeochromocytoma
Sweating, headache, HT, anxiety, SOB, weight loss, tachycardia, pallor, hyperglycaemia, low K, high Ca
NF1
Neurofibromas, cafe au lait macules, axillary freckling