Pheochromocytoma laboratory findings: Difference between revisions
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{{Pheochromocytoma}} | {{Pheochromocytoma}} | ||
{{CMG}} | {{CMG}} {{AE}} {{AAM}} | ||
==Overview== | ==Overview== | ||
Laboratory findings consistent with the diagnosis of pheochromocytoma include elevated [[catecholamines]] and [[metanephrine]] levels | Laboratory findings consistent with the diagnosis of pheochromocytoma include elevated [[catecholamines]] and [[metanephrine]] levels. | ||
==Laboratory Findings== | ==Laboratory Findings== | ||
The diagnosis can be established by measuring [[catecholamine]]s and [[metanephrine]]s in plasma or through a 24-hour urine collection. Urinary [[vanillyl mandelic acid]] may be elevated. | The diagnosis can be established by measuring [[catecholamine]]s and [[metanephrine]]s in plasma or through a 24-hour urine collection. Urinary [[vanillyl mandelic acid]] may be elevated. | ||
Revision as of 14:49, 2 September 2015
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Risk calculators and risk factors for Pheochromocytoma laboratory findings |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Laboratory findings consistent with the diagnosis of pheochromocytoma include elevated catecholamines and metanephrine levels.
Laboratory Findings
The diagnosis can be established by measuring catecholamines and metanephrines in plasma or through a 24-hour urine collection. Urinary vanillyl mandelic acid may be elevated.