This webinar will cover a basic overview of paraganglioma/pheochromocytoma (PPGL), its’ association with hereditary cancer syndromes, and management of associated syndromes. A specific focus on genetic testing will be addressed, denoting the high rate of pathogenic variants in PPGL and characteristics that increase or decrease likelihood of pathogenic findings. Additional information on specific hereditary PPGL syndromes will be described in detail, as well as updates to NCCN guidelines and recent literature.
Level of Instruction: Intermediate