ea0026p585 | Clinical case reports | ECE2011
Zuhur Sayid Shafi
, Karaman Ozcan
, Yildirim Sumeyra
, Erdamar Sibel
, Senturk Hakan
, Altuntas Yuksel
Background: MEN-1 is a rare disease characterized by parathyroid adenoma or hyperplasia, pituitary adenoma and pancreatic neuroendocrine tumors (PNET). Gastrinomas are the most common functional PNET in MEN-1 disease. Insulinomas and glucagonomas constitute approximately 20 and 3% of PNETs in MEN-1 disease. Most of insulinomas are benign in nature but about 70% of cases of glucagonomas present with metastasis at diagnosis. Coexistence of various PNETs are very rare...