Abstract Library

#2254 Development of a Patient-Centred Service for Neuroendocrine Tumors (NETs) in Wales: Population Based National Commissioning

Introduction: Requiring many specialities and services, NETs have complex pathways presenting a challenge to plan services in existing NHS structures

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author:

Authors: Khan M, Reynolds M, Lewis J, Bell C, Rees A,

Keywords: Service, commissioning, Mdt,

#2147 Nutritional Assessment and Vitamin Deficiencies in Patients with NETs

Introduction: As a result of disease or related to its management, patients with neuroendocrine tumours may have altered gut or pancreatic function that can cause nutritional deficiencies.

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author:

Authors: Lim S, Reynolds M, Rees D, Chaudhry R, Blackhouse J,

Keywords: Nutrition, Dietetics, Malnutrition, Vitamin Deficiency, Screening,

#2020 Expression of Somatostatin Receptors in Neuroendocrine Tumors of the Lungs with Various Degrees of Malignancy

Introduction: Diagnostics and management of patients with neuroendocrine tumors of the lung requires an individual approach

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author:

Authors: Gurevich L, Korsakova N, Voronkova I, Kazantseva I, Ashevskaya V,

Keywords: lungs, neuroendocrine tumors, somatostatin receptor, differentiation,

#1523 Multiregion Analysis Reveal Evolutionary Patterns and a Chromosomal Instability Signature in Pancreatic Neuroendocrine Tumours

Introduction: Pancreatic neuroendocrine tumors (PNETs) are potentially lethal diseases that show variable degrees of proliferation and invasiveness. Although genetic subgroups have been suggested to give prognostic information the impact of clonal evolution to the development and outcome of PNETs remains unexplored.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author: Crona J

Authors: Crona J, Backman S, Kugelberg J, Maharjan R, Björklund P,

Keywords: Cancer evolution, Molecular genetics, Neuroendocrine Tumor,

#262 Changes on Chromosome 18 are Involved in Sporadic and Familial Ileal Carcinoid Tumor Development

Introduction: Small intestine neuroendocrine tumors (ileal carcinoid) is generally considered a sporadic disease. We have identified nine families with an ileal carcinoid tumor diagnosed in two or more individuals.

Conference: 8th Annual ENETSConcerence (2011)

Presenting Author:

Authors: Tiensuu Janson E, Cunningham J, Diaz de Ståhl T, Sjöblom T, Westin G,

Keywords: genetics, ileal carcinoid, familial, pedigrees,