Abstract Library

#3090 Retrospective Experience with Pherochromocytoma (PH) and Paraganglioma (PG) in a Single Argentinian Institution

Introduction: Pherochromocytoma (PH) and paraganglioma (PG) are neuroendocrine tumors arising in cromaffin cells in the adrenal medulla or extra adrenal paraganglia respectively. Clinical presentation is diverse. All PG/PH have malignant potential. Hereditary cases comprise up to 40% of all PG/PH.

Conference: 17th Annual ENETSConcerence (2020)

Presenting Author:

Authors: Dioca M, Calabretta M, Iglesias L, Rojas Bilbao E, Califano I,

Keywords: Pherochromocytoma and paraganglioma (PG),

#2064 The Difficulties in Managing Metastatic Pancreatic Neuroendocrine Tumours (pNETs) Causing Cushing’s Syndrome (CS)

Introduction: The pNETs causing CS are very rare and aggressive. Despite the use of various therapeutic modalities, their management is not well-established, representing nowadays a challenge.

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author:

Authors: Simó-Servat A, Teulé A, Sánchez C, Díez J, Iglesias P,

Keywords: pNETs, cushing syndrome,

#929 Prognostic Role of Smoking in Gastroenteropancreatic Neuroendocrine Tumors (GEP-NET)

Introduction: Large retrospective series identified several prognostic factors for GEP-NET such as sex, race, age, primary localization, stage or tumor grade. Several studies suggested a prognostic role of smoking in many cancer types. However, no data has been reported in GEP-NET.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author:

Authors: Pons F, Mar I, Gallego , Luque A, González ,

Keywords: smoking, prognostic, gastroenteropancreatic, neuroendocrine tumor,