Abstract Library

#2738 Patient-Derived Organoid Models of Human Neuroendocrine Carcinoma

Introduction: Gastroenteropancreatic neuroendocrine carcinoma (GEP-NEC) is a poorly understood disease with limited treatment options. Due to its low incidence and wide tissue distribution few representative preclinical models are available

Conference: 17th Annual ENETSConcerence (2020)

Presenting Author: Tesselaar M

Authors: Dijkstra K, van den Berg J, Weber F, van de Haar J, Velds A,

Keywords: organoids, gastroenteropancreatic neuroendocrine carcinoma (GEP-NEC), disease modeling, pre-clinical models,

#1703 NeuroEndocrine Tumors of The Ampullary Region: A Rare Challenging Entity

Introduction: NeuroEndocrine Tumors (NETs) of the ampulla of Vater are rare.

Conference: 14th Annual ENETSConcerence (2017)

Presenting Author:

Authors: Milanetto A, Liço V, Alaggio R, Pasquali C,

Keywords: gastro-entero-pancreatic neuroendocrine tumors, ampulla of Vater,

#1477 Neuroendocrine Tumors of the Biliary Tract: A Retrospective, Observational Multicenter Study

Introduction: Neuroendocrine tumors of the biliary tract (BTNETs) constitute a heterogeneous group of neoplasms. Because of their rarity, the clinical behavior is unclear.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author:

Authors: Brizzi M, Massironi S, Pusceddu S, De Nigris B, Birocco N,

Keywords: Biliary tract NET,

#729 Neuroendocrine Neoplasms of the Ampulla of Vater: Clinicopathological Analysis of Nine Cases

Introduction: Neuroendocrine neoplasms (NEN) of the ampulla of Vater (AV) are rare and heterogeneous and little is known about their biological behavior.

Conference: 10th Annual ENETSConcerence (2013)

Presenting Author:

Authors: Perez-Casanova L, Meléndez C, Serrano T, Valls C, Fabregat J,

Keywords: ampulla, neuroendocrine,

#279 Coexistence of a Somatostatin-Producing Carcinoma of Duodenum and a Jejuna Gastrointestinal Stromal Tumor (GIST) in a Patient with Von Recklinghausen’s Disease

Introduction: Duodenal neuroendocrine tumors comprise 2-3% of all neuroendocrine tumors of the gastrointestinal tract. Coexistence of NF-1, NET and GIST is rare and only five cases have been described in the literature.

Conference: 8th Annual ENETSConcerence (2011)

Presenting Author:

Authors: Daraki V, Stamou K, ?amalaki E, Spyrou F, Kalikakis G,

Keywords: somatostatinoma, Neurofibromatosis Type 1 , GIST, ,