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Pheochromocytoma.

M S Eigelberger·Q Y Duh
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Abstract

The only definitive therapy for patients with pheochromocytoma is surgical resection [1,2**]. Advances in preoperative medical management of hypertension/hypovolemia and improved intraoperative anesthetic care have reduced the operative mortality rate for pheochromocytoma to less than 5% in most series. In addition, accurate preoperative localization studies have eliminated the need for extensive exploratory laparotomy. Focused approach and laparoscopic resection have become the new "gold standard," with a reduced morbidity [4**]. Large or locally invasive pheochromocytomas may still require open resection.

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3-IodobenzylguanidineAdrenal Gland NeoplasmsAdrenal MedullaAdrenalectomyAdrenergic alpha-AntagonistsAntihypertensive AgentsAntineoplastic Combined Chemotherapy ProtocolsCatecholaminesDiagnostic ImagingHumansHypertensionLaparoscopyMetanephrineNeoplastic Syndromes, HereditaryPalliative CarePheochromocytomaTachycardiaJournal ArticleReview

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M S Eigelberger, Q Y Duh. 2001. Pheochromocytoma.. https://doi.org/10.1007/s11864-001-0025-5

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