Pheochromocytoma/Paraganglioma: Update on Diagnosis and Management

After more than a century since they were described, pheochromocytomas and paragangliomas (PHEOs/PGLs) still pose great diagnostic and therapeutic challenges. Recent discoveries and progress in the understanding of molecular and metabolic changes associated with tumorigenesis allowed us to get closer to deciphering the secrets of these tumors. New knowledge allows us to develop novel diagnostic methods and identify specific treatment targets to improve the care of PHEO/PGL patients.