Abstract Library

#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,

#1866 NET – Incidental Findings: Small, Silent and Innocent?

Introduction: Neuroendocrine tumours (NETs) are rare neoplasms, with an overall incidence of 2 cases per 100,000 individuals per year. This number is increasing due to improved diagnosis, classification and higher imaging sensitivity, which lead to discovering of small and clinically insignificant NETs.

Conference: 14th Annual ENETSConcerence (2017)

Presenting Author: Roque R

Authors: Peralta Ferreira M, Strecht J, Alberto Teixeira J, Glória L, Roque R,

Keywords: NET, incidentaloma,

#1530 Bizarre Neuroendocrine Tumour Presentations

Introduction: Herein we present two cases of neuroendocrine tumours (NET)with atypical presentations.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author: Palmela C

Authors: Palmela C, Cunha C, Costa Santos M, Glória L, Roque R,

Keywords: cutaneous metastasis, GI bleeding,

#1469 Theragnostic Approach of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NET) – The Role of Nuclear Medicine (NM) in a Multidisciplinary Team

Introduction: NET pts are a clinical challenge requiring intervention of multiple medical specialties

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author: Lucio T

Authors: Lucio T, Gaspar C, Cunha C, Roque R, Glória L,

Keywords: PRRT, GEP-NET,

#1131 M-TORC1 Complex Is Significantly Over-Activated in SDHx-Mutated Paragangliomas

Introduction: The activation patterns of mTOR pathway in sporadic and hereditary pheochromocytomas (PCC) and paragangliomas (PGL) are poorly recognized.

Conference: 12th Annual ENETSConcerence (2015)

Presenting Author: Volante M

Authors: Oudijk L, Papathomas T, De Krijger R, Gimenez-Roqueplo A, Mannelli M,

Keywords: PCC, PGL, mTOR, SDHx,