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Pheochromocytoma Diagnosis

Biochemical Diagnosis

Initial testing for pheochromocytoma should include measurements of metanephrines (metabolic products of catecholamines) in blood, urine, or both. Elevation of more than 4-fold above the upper reference intervals is associated with close to 100% probability of pheochromocytoma or paraganglioma.

Tumor Localization Testing

Tumor localization testing should only be initiated if the biochemical test results indicate a relatively high probability of pheochromocytoma, except in patients with a hereditary predisposition or a previous history of the tumor. Computed tomography (CT) or magnetic resonance imaging (MRI) is the recommended method used for initial tumor localization. MRI is preferred in:

  • Children or pregnant women due to concerns regarding radiation exposure
  • Patients allergic to CT contrast dye
  • Situations where no additional radiation exposure is desired
  • Detection of extra-adrenal pheochromocytoma in a very unusual location


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The health information contained herein is provided for educational purposes only and is not intended to replace discussions with a healthcare provider. Decisions regarding patient care must be made with a healthcare provider, to consider the unique characteristics of the patient.

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