A 2019 review provided an in-depth analysis of postoperative management strategies for patients undergoing pheochromocytoma and paraganglioma (PPGL) resection. The review outlined the complex perioperative hemodynamic challenges associated with these tumors, particularly the abrupt fluctuations in catecholamine levels during and after surgery. Methods for managing postoperative complications were extensively discussed, including the use of intravenous fluids, vasopressors, and antihypertensive agents to stabilize blood pressure. The review emphasized the importance of a multidisciplinary approach involving endocrinologists, anesthesiologists, and intensivists to mitigate cardiovascular risks such as hypertensive crises, hypotension, arrhythmias, and myocardial infarctions. Perioperative hypertension following PPGL resection requires prompt management with short-acting and easily titratable agents. Phentolamine, administered as a 5 mg intravenous bolus and maintenance dose of 0.5 mg/min, is commonly used to counter hypertensive crises during and after surgery. To mitigate reflex tachycardia associated with α-adrenoceptor blockade, esmolol is often co-administered, starting with a loading dose of 0.5–1.0 mg/kg followed by an infusion titrated to effect. Alternative options such as nicardipine, clevidipine, nitroglycerin, and magnesium sulfate provide additional strategies for blood pressure control, particularly in patients with contraindications to β-blockade. [1]