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Secretory neuroendocrine tumors are usually associated with much higher levels of catecholamines than the upper limit of the established norm.
Pheochromocytoma The most common catecholamine-secretory (adrenaline and noradrenaline) is a tumor, which in 90% of cases is located in the medullary (brain) part of the adrenal gland. This type of tumor can occur alone or in the form of multiple endocrine neoplasms. The clinical picture includes hypertension, often marked by paroxysmal attacks, accompanied by tachycardia, chest pain, paleness, headache, nausea.
Other types of tumors that can occasionally cause paroxysmal or persistent hypertension are: Paraganglioma.
The test contains 3 fractions of free catecholamines (unconjugated) (adrenaline, noradrenaline and dopamine) in 24-hour urine and is an informative tool for diagnosing pheochromocytoma and other tumors of neural origin.
It is usually used as a confirmatory test if an elevated amount of methanephrine is detected in plasma or urine.
The diagnostic value is higher if samples are taken during a hypertensive crisis. Because the production of catecholamines by tumor cells is interrupted, the determination of catecholamines in 24-hour urine is more informative than testing them in plasma.
Sampling:
Container required for collection: 2-3 liter container and disposable plastic cup for urine, on which is placed (marked) the total amount of urine in 24 hours.
Increased levels of catecholamines in the urine:
Testing process
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