Pheochromocytoma (PCC) is a neuroendocrine tumor of the medulla of the adrenal glands (originating in the chromaffin cells), or extra-adrenal chromaffin tissue that failed to involute after birth that secretes high amounts of catecholamines. Its a hereditary disorder. Surgical resection of the tumor is the treatment of first choice, either by open laparotomy or laparoscopy