Pheochromocytoma Flashcards

1
Q

Signs of pheochromocytoma that merit screening

A

episodic headaches,

diaphoresis,

tachycardia hyperadrenergic spells (nonexertional palpitations, pallor)

resistant HTN

onset of HTN at young age

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2
Q

Need to screen for pheochromocytoma based on family history risk factors for pheochromocytoma

A

family history of pheochromocytoma predisposing familial syndrome (MEN2 and NF1 and VHL)

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3
Q

other reasons to screen for pheochromocytoma

A

adrenal incidentaloma on imaging pressor response during surgery or anethesia idiopathic dilated cardiomyopathy

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4
Q

if someone has unexplained idiopathic dilated cardiomyopathy need to consider

A

pheochromocytoma

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5
Q

if someone has disproportionate pressor response in surgery or gets afib with RVR need to consider

A

pheochromocytoma

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6
Q

if someone w/ headaches and anxiety develops hypertensive crisis and flash pulm edema or afib with RVR after anesthesia need to consider

A

pheochromocytoma

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7
Q

when do we see pheochromocytoma

A

>40 yrs but diagnosed at 50’s

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8
Q

sometimes symptoms of pheochromocytoma are unmasked by:

A

precipitating factor like anesthesia induction, pregnancy and physical activity

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9
Q

classic triad of pheochromocytoma is

A

headache, diaphoresis, palpitations 50% have paroxysmal HTN 95% of tumors are in the abdomen 85% are in adrenals.

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10
Q

10 percent rule of adrenal pheochromocytoma

A

10% in adrenals 10% malignant 10% are bilateral

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11
Q

test to order if you have highest pretest probability

A

order both urine and plasma metanephrines and (catecholamines too)

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12
Q

in pts who have low pretest probability, should order

A

urine catecholamines and if negative can rule out pheochromocytoma

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13
Q

If positive urine or serum catecholamines and metanephrines, need to follow this with

A

abdominal imaging CT scan or MRI

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14
Q

If imaging is unremarkable after positive screening testing with catecholamines/metanephrines and concerned for pheochromocytoma, need to look for:

A

radiolabeled metaiodobenzylguanidine to locate tumor

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15
Q

Treatment of pheochromocytoma is:

A

pre operative alpha blockade (phenoxybenzamine 10 mg PO bid) followed by low dose beta blocker (propranolol) titrated to heart rate and surgical resection and adrenalectomy (not always curative)

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16
Q

Algorithm for pheochromocytoma

A