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Saudi J Anaesth
; 16(2): 240-242, 2022.
Article
in English
| MEDLINE
| ID: mdl-35431728
ABSTRACT
Pheochromocytoma are catecholamine-producing neuroendocrine tumors that can be adrenal or extra-adrenal (paraganglioma) in origin. The mainstay of definitive therapy is surgical resection, and successful management depends on careful preoperative optimization, meticulous intraoperative and postoperative hemodynamic management.