A pheochromocytoma is a tumor of chromaffin cells that originates from either the adrenal medulla or extra-adrenal sympathetic tissues. The diagnosis of pheochromocytoma is based on elevated concentrations of plasma and urinary catecholamines or their metabolites. In most patients, the anatomic localization of the tumor is determined with computed tomography or magnetic resonance imaging. However, metaiodobenzylguanidine-scintigraphy or positron emission tomography (PET) can also easily identify the foci of neuroendocrine tumors. We diagnosed a patient with pheochromocytoma and high urinary norepinephrine levels, whose PET images revealed diffuse 18F-fluoro-2-deoxy-D-glucose (18FDG) accumulation in the shoulder, lower neck, and perivertebra...