
Urinary catecholamines and their metabolites are important signaling mediators in normal physiological processes. Changes in their concentrations in 24-hour urine are closely associated with a variety of pathological conditions.
Pheochromocytomas and paragangliomas synthesize, secrete, and release excessive amounts of catecholamines. Depending on the quantity, type, and form of catecholamine secretion, patients may present with different clinical manifestations.
The incidence of pheochromocytoma and paraganglioma is approximately 2–5 cases per million people per year. Among patients with hypertension, these tumors account for 0.1%–0.6% of cases, whereas the detection rate in autopsy reports is approximately 0.05%, suggesting that many cases remain undiagnosed.
Because missed diagnosis of pheochromocytoma and paraganglioma may lead to severe cardiovascular complications, early diagnosis is particularly important. Clinically, measurement of epinephrine (E), norepinephrine (NE), dopamine (DA), metanephrine (MN), normetanephrine (NMN), and 3-methoxytyramine (3-MT) in 24-hour urine is a primary basis for the qualitative diagnosis of pheochromocytoma and paraganglioma.

