ea0104p31 | Adrenal & Cardiovascular | SFEIES24
Nasar Khan Aida
, Khan Farooq
, Ryan James
Introduction: Pheochromocytomas are rare catecholamine-secreting tumors, primarily arising from the adrenal medulla, typically presenting with hypertension, palpitations, and headaches. Diagnosis involves hormonal evaluation and CT imaging with a washout of <40-60%. Recent studies show exceptions, with some tumours mimicking non-functional adenomas, displaying >60% washout. We present a case exemplifying this, where a symptomatic patient had normal initial biochemical ...