1. • A review of the patient’s family history helps identify hereditary syndromes.

2. Laboratory Tests:

   • Blood Tests: Measure hormone levels, including catecholamines and metanephrines.
   • Urine Tests: Check for hormone levels.

3. Imaging Studies:

   • CT Scan: Used to visualize the tumor.
   • Magnetic Resonance Imaging (MRI): Helps detect tumors or other conditions.
   • M-iodobenzylguanidine (MIBG) Imaging: Detects radioactive substances taken up by the tumor.
   • Positron Emission Tomography (PET): Also detects radioactive substances in the tumor.

4. Genetic Testing:

   • Determines if the tumor is part of an inherited syndrome by looking for specific genetic mutations.

5. Treatment Options:

   • Surgical removal of the tumor is the primary choice.
   • Medication may be needed to manage symptoms.
   • Chemotherapy or radiation therapy may be used for malignant pheochromocytomas.

6. Specialists Involved:

   • Endocrinologist: Specializes in endocrine system disorders.
   • Surgeon: Performs medical operations.

Remember, if you or someone you know shows symptoms of pheochromocytoma (such as high blood pressure, palpitations, sweating, or headache), seek medical attention promptly1.{% if Copilot_language == “Español” %} ¡Espero que esta información te sea útil!{% elif Copilot_language == “Français” %} J’espère que ces informations vous seront utiles !{% elif Copilot_language == “Deutsch” %} Ich hoffe, diese Informationen sind hilfreich!{% endif %}