ABSITE Review - Adrenal Flashcards

1
Q

What is the arterial supply to the adrenals?

A

Inferior phrenic artery, aorta and renal artery

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2
Q

What is the venous drainage of the adrenals?

A

Left adrenal vein goe to left renal vein; and Right adrenal vein goes to IVC.

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3
Q

When is an adrenalectomy indicated?

A

If mass has ominous characteristics (nonhomogenous) or is >4-6cm, functioning or enlarging

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4
Q

What is th work up needed for an adrenal incidentaloma?

A

Serum K, urine metanephrines/VMA/catecholamines, urinary hydroxycorticosteroids, plasma renin and aldosterone levels if HTN or low K
CXR stool guaiac and colonoscopy, mammogram

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5
Q

What are some common metastases to the adrenal gland?

A

Lung CA (#1), breast CA, melanoma, renal CA

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6
Q

What are the layers of the adrenal cortex and what they produce?

A

Glomerulosa - aldosterone; Fasciculata - Glucocorticoids; Reticularis - Androgens/Estrogens

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7
Q

What is the inital compound use by the adrenal?

A

Cholesterol

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8
Q

What is the function of aldosterone?

A

Stimulates renal Na resorption and secretion of K , hydrogen ions and ammonia

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9
Q

What stimulates the secretion of aldosterone?

A

Angiotensin II an hyperkalemia, and to some extent ACTH

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10
Q

What is the MC enzyme deficiency in congenital adrenal hyperplasia? What is the MC symptoms?

A

21-hydroxylase deficiency
Sxs: Precocius puberty in males, virilization in females, increase in 17-OH progesterone lead to increase prod of testosterone, Salt-wasting

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11
Q

What is the second MC enzyme deficiency in congenital adrenal hyperplasia? What is the MC symptoms?

A

11-hydroxylase deficiency

Sxs: precocious puberty in males, virilization in females, increase 11-deoxycortisone, Salt-saving

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12
Q

What are some causes of Primary hyperaldosteronism?

A

Adenoma (80-90%), Hyperplasia (10-20%), ovarian tumors, cancer

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13
Q

What are some causes of Secondary hyperaldosteronism?

A

More common than primary disease

CHF, renal artery stenosis, liver failure, pregnancy, diuretics, Bartter’s syndrome (renin-secreting tumor)

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14
Q

What is the main diagnostic test to differentiate between Primary and Secondary Hyperaldosteronism?

A

Primary - low renin

Secondary - high renin

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15
Q

What is the main diagnostic findings of Primary Hyperaldosteronism?

A

Urine aldosterone after salt-load (will stay high)
Low serum K, High urine K, High serum Na, Metabolic Alkalosis
Plasma renin activity will be low
Aldosterone:renin ratio > 20

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16
Q

What are some localizing studies that can be used for Primary Hyperaldosteronism?

A

MRI, NP-59 scintigraphy (differentiate adenoma from hyperplasia), adrenal venous sampling

17
Q

What is the treatment for Primary Hyperaldosteronism?

A

Adenoma - resection
Hyperplasia - Medical therapy first with spironolactone, CCBs, K
If bilateral resection is performed (usually done for refractory hypoK), pt will need fludrocortisone postop

18
Q

What is the #1 cause of adrenal insufficiency?

A

Withdrawal of exogenous steroids

19
Q

What is the #1 primary disease of adrenal insufficiency?

A

Autoimmune disease

20
Q

What diagnostic findings are seen in adrenal insufficiency?

A

Low serum Na, High serum K, ACTH stimulation test

21
Q

What step by step work up done for hypercortisolism?

A

1st - 24-hour urine cortisol (most sensitive test)
2nd - low-dose overnight dexamethasone suppression test. If cortisol is low, the dx is Cushing’s disease; if high, go to 3rd.
3rd - measure serum ACTH. If high, dx is either ectopic ACTH or pituitary tumor –> go to 4th; if low, pt has cortisol-secreting tumor.
4th - High-dose overnight dexamethasone suppression test. Positive = pituitary origin; negatiove = ectopic origin of ACTH.
5th - CRH test –> pituitary adenomas will increase ACTH; ectopic producers will have no change in ACTH

22
Q

What is the #1 cause of noniatrogenic cause of Cushing’s syndrome?

A

Cushing’s disease (Pituitary adenoma) 70-80% cases

23
Q

What is the #2 cause of noniatrogenic cause of Cushing’s syndrome?

A

Ectopic ACTH - most commonly small cell lung CA

24
Q

When is an bilateral adrenalectomy needed?

A

Adrenal hyperplasia, pts with ectopic ACTH from tumor that is unresectable or from pituitary adenoma that cannot be found

25
Q

What is the AA needed for catecholamine production?

A

Tyrosine

26
Q

What is the reta-limiting step enzyme in catecholamine production?

A

Tyrosine hydroxylase (tyrosine to dopa)

27
Q

What is the enzyme tha converts norepinephrine to epinephrine?

A

PNMT which is only found in the adrenal medulla

28
Q

In addition to the adrenal gland, where can pheochromocytomas be found?

A

Organ of Zuckerkandl

29
Q

From which cells, the pheochromocytomas originate?

A

Chromaffin cells

30
Q

What is the 10% rule of pheochromocytomas?

A

10% malignant, 10% bilateral, 10% in children, 10% familial, 10% extra-adrenal

31
Q

Which side of adrenal gland are pheochromocytomas most commonly found?

A

Right side

32
Q

What diagnostic studies are used for pheochromocytoma?

A

VMA most sensitive
MIBG scan
Clonidine suppression test

33
Q

What preoperative preparation is need for pheochromocytoma?

A

Volume replacement, alpha-blockade first (phenoxybenzamine –> avoids HTN crisis); then beta-blocker if patient has tachycardia or arrhythmias

34
Q

What happens if you give beta-blockade before alpha-blockade?

A

HTN crisis that can leed to heart failure

35
Q

During surgery, what maneuver can be done to avoid spilling of catecholamines?

A

Ligate adrenal veins first

36
Q

What can falsely elevated VMA?

A

Coffee, Tea, Fruits, Vanilla, Iodine contrast, Labetalol, alpaha and beta-blockers