Pheochromocytoma= A rare catecholamine producing tumour that originate from chromaffin cells in the adrenal medulla. Patients classically present with: paroxysmal hypertension, palpitations, headache, and diaphoresis. The frequency varies from daily, weekly or monthly. Patients generally have orthostatic hypotension on physical exam.
NOTE: Surgery is the definitive treatment. Pre-operatively the patient must be given both alpha- AND beta-blocking agents!
WARNING: Never give a patient with a pheochromocytoma a beta-blocker without first giving an alpha-blocker!!!
REFERENCES
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