Pheochromocytoma and functional paraganglioma

Curr Opin Oncol. 2004 Jan;16(1):8-12. doi: 10.1097/00001622-200401000-00003.

Abstract

Purpose: 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.

Publication types

  • Review

MeSH terms

  • Adrenal Gland Neoplasms / epidemiology
  • Adrenal Gland Neoplasms / physiopathology*
  • Adrenal Gland Neoplasms / radiotherapy
  • Diagnosis, Differential
  • Humans
  • Hypertension / etiology
  • Paraganglioma / diagnosis
  • Paraganglioma / epidemiology
  • Paraganglioma / physiopathology*
  • Pheochromocytoma / epidemiology
  • Pheochromocytoma / physiopathology*
  • Pheochromocytoma / radiotherapy
  • Radiopharmaceuticals / therapeutic use

Substances

  • Radiopharmaceuticals