📢 The Call for Abstracts for the 47th Annual Meeting of the AAES is now open!
Join us in Sacramento, California, from May 22-24, 2027 and share your latest research and innovations in endocrine surgery. buff.ly/VRbxuBy
How are pheochromocytomas and paragangliomas diagnosed?
Doctors may use:
✅ Blood or urine tests to check hormone levels
✅ Imaging (CT, MRI, or specialized scans) to locate the tumor
Everyone with pheo/para needs genetic testing! Up to 40% are linked to inherited syndromes.
Most pheochromocytomas and paragangliomas are treated with surgery to safely remove the tumor. Preparation with medication before surgery is critical to control blood pressure and prevent complications.@PheoParaAlliance Centers of Excellence can be a great resource. See an expert
Pheochromocytoma ("pheos") secrete catecholamines which cause “spells” of high BP, headache, heart racing, sweating, and/or anxiety. These symptoms can be difficult to diagnose with such a rare disease. @PheoParaAlliance #TheAdrenalineRush#PheoParaPhorever#PheoParaPhearless
Join us tonight with this expert @TheAAES lineup for @PheoParaAlliance Awareness Week! Join us 8 pm EST/5 pm PST for the live event. #PheoPara#AdrenalineRush