Adrenals Flashcards

1
Q

Do steroid hormones have a fast or slow response to a stimulus?

A

Slow - bound to plasma proteins

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2
Q

Functions of AT II

A

Stimulates aldosterone

Increases water reabsorption

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3
Q

Conn’s syndrome

A

Hypersecretion of aldosterone due to tumour in glomerulosa

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4
Q

Diagnosis of CAH (bilateral) and Conn’s (unilateral)

A

Aldosterone:Renin ratio (>750)

Saline suppression test (increased aldosterone)

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5
Q

Treatment of Conn’s and CAH

A

Conn’s (unilateral): surgery

CAH (bilateral): spironolactone (aldosterone rec antagonist)

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6
Q

Effects of cortisol

A

Increased lipolysis, decreased glucose uptake, increased gluconeogenesis (liver), increased muscle proteolysis, increased responsiveness to AD = increased CO, decreased Ob activity

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7
Q

Symptoms of cortisol hypersecretion (Cushing’s)

A

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

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8
Q

ACTH dependent Cushing’s

A

Pituitary adenoma = increased ACTH
Headaches, visual field impairment, acne, amenorrhea, frontal balding (high testosterone)
Ectopic ACTH from cancer (small cell)

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9
Q

ACTH independent Cushing’s

A

Adrenal adenoma/carcinoma, hyperplasia

Low ACTH

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10
Q

Diagnosis of Cushing’s

A

Low dose dexamethasone suppression test = high cortisol levels
High dose dexamethasone suppression test: high cortisol levels = adrenal/ectopic, low cortisol levels = pituitary
DEXA

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11
Q

Treatment of Cushing’s

A

Metyrapone
Ketoconazole
Surgery

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12
Q

Effects of adrenaline

A
Increase HR and force (B1)
Vasoconstriction (a1)
Vasodilation of skeletal muscle (B2)
Decreased insulin secretion (a2)
Increased gluconeogenesis and glycogenolysis (a1/B1)
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13
Q

Phaeochromocytoma

A

Catecholamine secreting tumour of adrenal medulla, arise from sympathetic paraganglia cells (chromaffin cells)

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14
Q

Phaeochromocytoma is associated with which condition?

A

MEN2 - bilateral, thyroid and parathyroid
NF1
Tuberous sclerosis
Von Hippel Lindau syndrome

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15
Q

Diagnosis of phaeochromocytoma

A

Urinary catecholamines, CT/MRI/MIBG/PET

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16
Q

Treatment of phaeochromocytoma

A

Surgery

Alpha (phenoxybenzamine) then Beta blockers (propanolol, atenolol)

17
Q

Treatment for Addisonian crisis

A

Glucose
Steroid replacement (IV hydrocortisone, fludrocortisone)
IV fluids

18
Q

Diagnosis of Addison’s

A

Short synacthen test (no rise in cortisol)

MRI

19
Q

Presentation of CAH

A

Salt losing crisis, ambiguous genitalia, increased androgens, decreased aldosterone, oligomenorrhoea, acne, hirsutism

20
Q

CAH

A

21a-hydroxylase deficiency = more testosterone, no cortisol/aldosterone
Auto Recessive

21
Q

Rate limiting step of steroid production

A

Cholesterol -> Pregnenolone

22
Q

How is aldosterone released?

A

Decreased BP activates RAAS, AT II causes aldosterone release and vasoconstriction

23
Q

Where are mineralocorticoid receptors?

A

Kidneys, salivary glands, gut, sweat glands

24
Q

Treatment for Addison’s

A

Hydrocortisone and Fludrocortisone

Sick day rules

25
Q

Symptoms of Addison’s

A

Anorexia, fatigue, weight loss, dizziness, low BP, abdo pain, N+V, skin pigmentation, decreased Na, increased K, high renin, low aldosterone

26
Q

Treatment for secondary adrenal insufficiency

A

Hydrocortisone only

27
Q

Symptoms of phaeochromocytoma

A

Sweating, headache, HT, anxiety, SOB, weight loss, tachycardia, pallor, hyperglycaemia, low K, high Ca

28
Q

NF1

A

Neurofibromas, cafe au lait macules, axillary freckling