Abstract Library

#4548 Carcinoid heart disease in patients with carcinoid syndrome and metastatic small intestinal neuroendocrine tumours: A single centre experience

Introduction: Carcinoid heart disease (CHD) is a significant complication of carcinoid syndrome (CS) in patients with small intestinal neuroendocrine tumours (SINET). Management is complex and more data is needed.

Conference:

Presenting Author:

Authors: Salman M, Waters M, Abbott C, Quinn M, O'Toole D,

Keywords: carcinoid heart disease, carcinoid syndrome, NET, neuroendocrine tumour, small intestinal NET,

#4100 Pheochromocytoma and paraganglioma: Gender differences in lipid profile

Introduction: Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine neoplasms potentially influencing lipid metabolism and increasing cardiovascular risk. Gender differences in PPGL are largely unknown.

Conference:

Presenting Author: Di Iasi G

Authors: Di Iasi G, Benevento E, Cannavale G, Liccardi A, Minotta R,

Keywords: gender, Pheochromocytoma, paraganglioma, lipid, cholesterol,

#3843 VIPoma presenting as chronic diarrhea in a 30-year-old Filipino female

Introduction: Pancreatic neuroendocrine tumors are rare neoplasms that arise in the endocrine tissues of the pancreas. They can secrete a variety of peptide hormones including insulin, gastrin, glucagon, and vasoactive intestinal peptide. Secretory tumors such as vasoactive intestinal polypeptides are rare neuroendocrine pancreatic neoplasms characterized by watery diarrhea, hypokalemia, and hypochlorhydria.

Conference:

Presenting Author: Edejer P

Authors: Edejer P, Mendoza R, Pascasio C, Lin T, Cornelio G,

Keywords: Pancreatic NET, Octreotide, DOTATATE, diarrhea,

#3675 Care trajectory, informational needs and challenges of patients with neuroendocrine tumors – A mixed methods study

Introduction: Patients with neuroendocrine tumors (NET) encounter different challenges, including delayed diagnosis and difficulty finding NET-specific information of high-quality.

Conference:

Presenting Author:

Authors: Bénard F, Mercier F, Huez S, Pomey M,

Keywords: neuroendocrine, cancer, needs, information, challenges,

#3583 Mixed Neuroendocrine-Non-Neuroendocrine Neoplasms (MiNEN): Characterization of the genomic and pathological profile

Introduction: A mixed non-neuroendocrine neoplasm (MiNEN) is a novel defined rare entity, made up of two morphologically distinct neoplastic components; one neuroendocrine type (NEN), and the other one non-neuroendocrine type (nNEN). As available data are limited, the epidemiology and controversial pathogenesis of MiNENs remain mostly unknown.

Conference:

Presenting Author:

Authors: Di Mauro A, Tatangelo F, Conte M, Cantile M, Scognamiglio G,

Keywords: minen neuroendocrine tumor, neuroendocrine, molecular biology, microsatellite instability, oncogenic mechanism, biomarker, oncology, minen tumor, neuroendocrine tumor, genoma sequencing,