ea0032p216 | Clinical case reports – Pituitary/Adrenal | ECE2013
Gruszka Anna
, Zieleniewski Wojciech
, Kotecka-Blicharz Agnieszka
, Jarzab Barbara
, Kunert-Radek Jolanta
Introduction: Pheochromocytomas are rare neuroendocrine tumors arising from chromaffin cells of the adrenal medulla. Approximately 10% of all pheochromocytomas are malignant. There is no effective therapy for malignant pheochromocytoma (MAL-PHEO) and the overall prognosis is poor.Case report: We report 22-year survival with MAL-PHEO in a patient treated with several surgeries, 131I-metaiodobenzylguanidine and, subsequently, with long-acting fo...