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What is Pheochromocytoma Overview and Management about?
Pheochromocytoma is a rare neuroendocrine tumor that originates from chromaffin cells of the adrenal medulla or extra-adrenal sympathetic ganglia. It secretes excess catecholamines, mainly epinephrine and norepinephrine. Clinical presentation includes paroxysmal or sustained hypertension, severe headaches, palpitations, and sweating. Biochemical testing involves measuring catecholamines and their metabolites in 24-hour urine or plasma samples. Localization of the tumor is typically done with CT or MRI imagi
- Author
- michael
- Language
- EN