A case of clinically silent giant right pheochromocytoma and review of literature

Abstract

Clinically silent giant cystic pheochromocytoma is a rare adrenal disease; complete resection is the only curative treatment. Due to the serious surgical risk, successful resection is very difficult. We report a case of a patient with giant cystic pheochromocytoma, which was successfully resected. There were no intraoperative and postoperative complications. We analyze and report our experience.

Fig 1

Post-contrast computed tomography axial plane shows the mass pressurizing liver forward and laterally. Outside area of the mass displays significant enhancement with uneven thickness. There is no evidence of local invasion.

Fig 2

Magnetic resonance imaging coronal plane shows a giant well-defining round cystic right adrenal mass, dislocating from the right kidney downward.

Fig 3

Magnetic resonance imaging axial plane demonstrates the mass with extensive cystic part.