Pheochromocytoma

Odessa R. Pulido, Lindsey Perea

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Pheochromocytoma is a rare tumor that has debilitating effects. These tumors originate from chromaffin cells and are located in the adrenal medulla. Tumors located outside of the adrenal medulla are known as paragangliomas. Patients usually suffer from episodes of hypertension, headaches, sweating, etc. This is due to excess circulating catecholamines. An adrenalectomy is the mainstay of treatment. However, appropriate management of hemodynamics in the perioperative period is key to a successful outcome.

Original languageAmerican English
Title of host publicationPassing the General Surgery Oral Board Exam
EditorsMarc Neff, Alec Beekley, Kahyun Yoon-Flannery, Asanthi Ratnasekera
PublisherSpringer
Pages209-210
Edition5
DOIs
StatePublished - Jan 1 2025

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