ea0040p18 | (1) | ESEBEC2016
Martins D
, Baptista C
, Rodrigues D
, Miguel Melo
, Cardoso L M
, Vicente N
, Oliveira D
, Ventura M
, Lages A
, Carrilho F
Introduction: Pheochromocytoma is a rare catecholamine-secreting tumor that arises from the chromaffin tissue of the adrenal medulla. Of the reported cases, only 10% consist in bilateral lesions and the probability of multiple endocrine neoplasia should always be investigated.Clinical case: Female patient, 19 years old, presented with a clinical history with 2 years of evolution, characterized by episodes of palpitations, headache, nausea and abdominal d...