Abstract Library

#2737 Identification of a Novel MAFA Missense Mutation Causing Familial Insulinomatosis

Introduction: Insulinomatosis is a rare pancreatic disease characterized by an adult-onset condition of recurrent hyperinsulinemic hypoglycemia caused by multiple insulin-secreting neuroendocrine tumors.

Conference: 17th Annual ENETSConcerence (2020)

Presenting Author: Fottner C

Authors: Fottner C, Sollfrank S, Ghiasi M, Ferrata M, Schad A,

Keywords: Insulinomatosis, Insulinoma, hyperinsulinemic hypoglycemia, MAFA,

#2218 More than Rare Pheochromocytomas: Bilateral and Hemorrhagic, Giant and Metastatic

Introduction: Pheochromocytomas (PCC) are rare neuroendocrine tumors. These catecholamine-secreting tumors, with an average size of 4.9cm, are multiple in 10% of cases. About 10% are malignant but distant metastases are rare. Non-traumatic adrenal hemorrhage is an unusual potentially fatal event seen in PCC.

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author: Peralta Ferreira M

Authors: Peralta Ferreira M, Sousa Fernandes M, Roque R, Matos C, Strecht J,

Keywords: pheochromocytoma, giant, hemorrhagic, metastatic, bilateral,