Abstract Library

#4071 Hospital record data on the clinical presentation and diagnostic investigations of small intestinal neuroendocrine tumors (SI-NETs)

Introduction: The diagnosis of small intestinal neuroendocrine tumors(SI-NETs) is often delayed due to non-specific symptoms, difficulty imaging, and lack of awareness.

Conference:

Presenting Author: Gould H

Authors: Gould H, Kapish A, Karategos T, Abbas S, Olive S,

Keywords: small intestinal neuroendocrine tumor, investigation, Colonoscopy, CT, presentation, symptoms, Diagnosis,

#3444 Earlier diagnosis of Neuroendocrine Tumors (NETs) through transformation of the South Wales NET Service

Introduction: Neuroendocrine tumors (NETs) are heterogeneous cancers, arising mainly from the gastroenteropancreatic tract. Delayed diagnosis and mislabelling are widely recognised internationally in midgut NETs with little data describing how to improve diagnosis times. In 2017, transformation of the South Wales NET Service included a change to a gastroenterology-led service model, alongside education and forming working relationships with gastroenterologists and surgeons.

Conference:

Presenting Author:

Authors: Gould H, Kapish A, Karategos T, Abbas S, Taylor R,

Keywords: midgut NET, midgut neuroendocrine tumor, diagnosis, diagnostic delay, investigation, mislabel, imaging,

#2124 A Case Report of a Malignant Insulinoma

Introduction: Despite rare (1-2% of pancreatic tumors/PT), insulinomas are the most common functional pNET. The diagnosis is established by demonstrating inappropriately high serum insulin levels during a spontaneous or induced episode of hypoglycemia.

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author:

Authors: Zoumblios C, Tegos T, Kyriakopoulos G, Argyrakos T, Alevizopoulos N,

Keywords: malignant, insulinoma,

#1930 Concomitant Intraductal Papillary Mucinous Neoplasms and Neuroendocrine Tumors of the Pancreas: More than just a Coincidence?

Introduction: Intraductal papillary mucinous neoplasms (IPMNs) and pancreatic neuroendocrine tumors (pNETs) are rare tumors. Up to now 14 patients with association of endocrine and exocrine neoplasms of the pancreas have been reported in literature: this association is not expected to be frequent

Conference: 14th Annual ENETSConcerence (2017)

Presenting Author: Cortegoso Valdivia P

Authors: Venezia L, Cortegoso Valdivia P, De Angelis C,

Keywords: IPMN, NET, pancreas,

#1928 Pancreatic Involvement in VHL Disease: The Turin Experience

Introduction: Von Hippel-Lindau disease (VHL) is a rare heritable genetic syndrome. Its typical manifestations concern CNS but it may affect other organs such as the pancreas.

Conference: 14th Annual ENETSConcerence (2017)

Presenting Author: Cortegoso Valdivia P

Authors: Cortegoso Valdivia P, Venezia L, De Angelis C,

Keywords: VHL,