1.
Saudi J Anaesth
; 16(2): 240-242, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35431728
RESUMO
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.