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Pheochromocytoma and functional paraganglioma

Roman S2004Current Opinion in OncologyReview

Abstract

Pheochromocytomas and paragangliomas are rare tumors of chromaffin cell origin. Their identification is likely increasing owing to the increased use of radiographic images detecting incidental adrenal masses. RECENT FINDINGS: The pathophysiology of hypertension induced by the release of catecholamines and newly discovered peptides has been shown to be more complex than the concept of episodic catecholamine release. SUMMARY: This review looks at the most recent advances in the physiology and molecular basis of these tumors.

Part of CIRS Nexus · Curated by Lauren Lowenstein, The Biotoxin Lady