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A pheochromocytoma
is a catecholamine-secreting tumor of chromaffin cells typically located
in the adrenals. It causes persistent or paroxysmal hypertension.
Diagnosis is by measuring catecholamine products in blood or urine.
Imaging tests, especially CT or MRI, help localize tumors. Treatment
involves removal of the tumor when possible. Drug therapy for control
of BP includes α-blockade,
usually combined with β-blockade.
The catecholamines secreted include norepinephrine, epinephrine, dopamine, and dopa in varying proportions. About 90% of pheochromocytomas are in the adrenal medulla, but they may also be located in other tissues derived from neural crest cells. Possible sites include the following:
Pheochromocytomas in the adrenal medulla occur equally in both sexes, are bilateral in 10% of cases (20% in children), and are malignant in < 10%. Of extra-adrenal tumors, 30% are malignant. Although pheochromocytomas occur at any age, peak incidence is between the 20s and 40s. About 25% are now thought to be due to germline mutations.
Pheochromocytomas vary in size but average 5 to 6 cm in diameter. They weigh 50 to 200 g, but tumors weighing several kg have been reported. Rarely, they are large enough to be palpated or cause symptoms due to pressure or obstruction. Regardless of the histologic appearance, the tumor is considered benign if it has not invaded the capsule and no metastases are found, although exceptions occur.
Pheochromocytomas may be part of the syndrome of familial multiple endocrine neoplasia (MEN), types IIA and IIB, in which other endocrine tumors (parathyroid or medullary carcinoma of the thyroid) coexist or develop subsequently (see Multiple Endocrine Neoplasia (MEN) Syndromes). Pheochromocytoma develops in 1% of patients with neurofibromatosis (von Recklinghausen's disease) and may occur with hemangiomas and renal cell carcinoma, as in von Hippel-Lindau disease. Familial pheochromocytomas and carotid body tumors may be due to mutations of the enzyme succinate dehydrogenase.
Symptoms and Signs
Hypertension, which is paroxysmal in 45% of patients, is prominent. About 1/1000 hypertensive patients has a pheochromocytoma. Common symptoms and signs are tachycardia, diaphoresis, postural hypotension, tachypnea, cold and clammy skin, severe headache, angina, palpitations, nausea, vomiting, epigastric pain, visual disturbances, dyspnea, paresthesias, constipation, and a sense of impending doom. Paroxysmal attacks may be provoked by palpation of the tumor, postural changes, abdominal compression or massage, induction of anesthesia, emotional trauma, unopposed β-blockade (which paradoxically increases BP by blocking β-mediated vasodilation), or micturition (if the tumor is in the bladder). In elderly patients, severe weight loss with persistent hypertension is suggestive of pheochromocytoma.
Physical examination, except for the presence of hypertension, is usually normal unless done during a paroxysmal attack. Retinopathy and cardiomegaly are often less severe than might be expected for the degree of hypertension, but a specific catecholamine cardiomyopathy can occur.
Diagnosis
Pheochromocytoma is suspected in patients with typical symptoms or particularly sudden, severe, or intermittent unexplained hypertension. Diagnosis involves demonstrating high levels of catecholamine products in the serum or urine.
Blood
tests:
Plasma free metanephrine is up to 99% sensitive. This test has superior sensitivity to measurement of circulating epinephrine and norepinephrine because plasma metanephrines are elevated continuously, unlike epinephrine and norepinephrine, which are secreted intermittently; however, grossly elevated plasma norepinephrine renders the diagnosis highly probable.
Urine tests:
Urinary metanephrine is less specific than plasma free metanephrine, but sensitivity is about 95%. Two or 3 normal results while the patient is hypertensive render the diagnosis extremely unlikely. Measurement of urinary norepinephrine and epinephrine is nearly as accurate. The principal urinary metabolic products of epinephrine and norepinephrine are the metanephrines vanillylmandelic acid (VMA) and homovanillic acid (HVA). Healthy people excrete only very small amounts of these substances. Normal values for 24 h are as follows: free epinephrine and norepinephrine < 100 μg (< 582 nmol), total metanephrine < 1.3 mg (< 7.1 μmol), VMA < 10 mg (< 50 μmol), HVA < 15 mg (< 82.4 μmol). In pheochromocytoma, increased urinary excretion of epinephrine and norepinephrine and their metabolic products is intermittent. Elevated excretion of these compounds may also occur in other disorders (eg, neuroblastoma, coma, dehydration, sleep apnea) or extreme stress; in patients being treated with rauwolfia alkaloids, methyldopa , or catecholamines; or after ingestion of foods containing large quantities of vanilla (especially if renal insufficiency is present).
Other tests:
Blood volume is constricted and may falsely elevate Hb and Hct levels. Hyperglycemia, glycosuria, or overt diabetes mellitus may be present, with elevated fasting levels of plasma free fatty acid and glycerol. Plasma insulin level is inappropriately low for the plasma glucose. After removal of the pheochromocytoma, hypoglycemia may occur, especially in patients treated with oral antihyperglycemics.
Provocative tests with histamine or tyramine are hazardous and should not be used. Glucagon 0.5 to 1 mg injected rapidly IV provokes a rise in BP > 35/25 mm Hg within 2 min in normotensive patients with pheochromocytoma but is now generally unnecessary. Phentolamine
mesylate must be available to terminate any hypertensive
crisis.
Screening tests are preferred to provocative tests. The general approach is to measure plasma metanephrines, 24-h urinary catecholamines or their metabolites as a screening test and to avoid provocative tests. In patients with elevated plasma catecholamines, a suppression test using oral clonidine or IV pentolinium can be used but is rarely necessary.
Imaging tests to
localize tumors are usually done in patients with abnormal screening results. Tests should include CT and MRI of the chest and abdomen with and without contrast. With isotonic contrast media, no adrenoceptor blockade is necessary. PET has also been used successfully. Repeated sampling of plasma catecholamine concentrations during catheterization of the vena cava with sampling at different locations, including the adrenal veins, can help localize the tumor: there will be a step up in norepinephrine level in a vein draining the tumor. Adrenal vein norepinephrine-to-epinephrine ratios may help in the hunt for a small adrenal source. Radiopharmaceuticals with nuclear imaging techniques can also help localize pheochromocytomas. 123I-metaiodobenzylguanidine (MIBG) is the most used compound outside the US; 0.5 mCi is injected IV and the patient is scanned on days 1, 2, and 3. Normal adrenal tissue rarely picks up this isotope, but 85% of pheochromocytomas do. The imaging is usually positive only when the lesion is large enough to be obvious on CT or MRI, but it can help confirm that a mass is likely to be the source of the catecholamines. 131I-MIBG is a less sensitive alternative.
Signs of an associated genetic disorder (eg, café-au-lait patches in neurofibromatosis) should be sought. Patients should be screened for MEN with a serum Ca (and possibly calcitonin ) and any other tests as directed by clinical findings.
Treatment
Surgical removal is the treatment of choice. The operation is usually delayed until hypertension is controlled by a combination of α- and β-blockers (usually phenoxybenzamine 20 to 40 mg po tid and propranolol 20 to 40 mg po tid). β-Blockers should not be used until adequate α-blockade has been achieved. Some α-blockers, such as doxazosin , may be equally effective but better tolerated.
The most effective and safest preoperative α-blockade is phenoxybenzamine 0.5 mg/kg IV in 0.9% saline over 2 h on each of the 3 days before the operation. Na nitroprusside can be infused for hypertensive crises preoperatively or intraoperatively. When bilateral tumors are documented or suspected (as in a patient with MEN), sufficient hydrocortisone (100 mg IV bid) given before and during surgery avoids acute glucocorticoid insufficiency from bilateral adrenalectomy.
Most pheochromocytomas can be removed laparoscopically. BP must be continuously monitored via an intra-arterial catheter, and volume status is closely monitored. Anesthesia should be induced with a nonarrhythmogenic drug (eg, a thiobarbiturate) and continued with enflurane. During surgery, paroxysms of hypertension should be controlled with injections of phentolamine 1 to 5 mg IV or nitroprusside infusion (2 to 4 μg/kg/min), and tachyarrhythmias should be controlled with propranolol 0.5 to 2 mg IV. If a muscle relaxant is needed, drugs that do not release histamine are preferred. Atropine should not be used preoperatively. Preoperative blood transfusion (1 to 2 units) may be given before the tumor is removed in anticipation of blood loss. If BP has been well controlled before surgery, a diet high in salt is recommended to increase blood volume. An infusion of norepinephrine 4 to 12 mg/L in a dextrose-containing solution should be started if hypotension develops. Some patients whose hypotension responds poorly to levarterenol may benefit from hydrocortisone 100 mg IV, but adequate fluid replacement is usually all that is required.
Malignant metastatic
pheochromocytoma should be treated with α- and β-blockers. The tumor may be indolent and survival long-lasting. However, even with rapid tumor growth, BP can be controlled. 131I-MIBG prolongs life when used to treat residual disease. Radiation therapy may reduce bone pain; chemotherapy is rarely effective but can be attempted if all else fails.
Last full review/revision November 2007 by Ashley B. Grossman, MD
Content last modified November 2007
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