Abstract Library

#4602 The role of microbiome diversity in neuroendocrine tumour (NET) development and progression: Insights from a cohort study

Introduction: The gut microbiome may influence neuroendocrine tumour (NET) development, particularly gastrointestinal NETs, yet data on this connection within Pakistan are limited. This study explores microbiome diversity’s role in NET progression.

Conference:

Presenting Author: Fatima A

Authors: Fatima A,

Keywords: Bacterial imbalance, Prognostic biomarker,

#4600 Artificial intelligence in predicting neuroendocrine tumour (NET) outcomes: A model-based prognostic approach

Introduction: Neuroendocrine tumours (NETs) vary widely in clinical behaviour, complicating prognosis. Traditional models often struggle with accuracy due to the complexity of NETs. Artificial intelligence (AI) offers tools for enhanced prognostic precision by analysing complex datasets. This study explores an AI-driven approach to predict outcomes in NET patients at Cantonment General Hospital, Pakistan.

Conference:

Presenting Author: Fatima A

Authors: Fatima A,

Keywords: artificial intelligence, machine learning, Precision medicine, Personalised treatment,

#4460 Digestive neuroendocrine tumours G1 and G2: Experience of the medical oncology department at the Oran University Hospital Establishment 1st November 1954

Introduction: The histological classification of neuroendocrine tumours (NETs) remains complex, and their grading is a major prognostic factor, essential for guiding appropriate management. Moreover, NETs raise unresolved histogenetic questions. The treatment of grade 1 (G1) NETs primarily relies on somatostatin analogues, while grade 2 (G2) NETs, being more heterogeneous, may require management that includes chemotherapy or targeted therapy.

Conference:

Presenting Author:

Authors: Kehili H, Bengueddache A, Boumansour N, Larbi Bounsbia L, Bechikh A,

Keywords: Digestive Neuroendocrine Tumour, Grade 1, Grade 2, Somatostatin Analogue,

#4218 Primary hepatic neuroendocrine tumor in a series of 8 cases

Introduction: Primary neuroendocrine (NET) tumors of the liver are extremely rare, accounting for 0.3% of all NETs; unlike metastatic neuroendocrine tumors, rarely cause carcinoid syndrome. Edmonson reported the first case in 1958. Since then, fewer than 150 cases have been reported in the literature. Before making the diagnosis of primary hepatic neuroendocrine tumor it is imperative to explore the patients, several radiological investigations can help to pinpoint the primary which is most often digestive.

Conference:

Presenting Author:

Authors: Samia K, Fatima H, Benali T, Nabil B, Aisha B,

Keywords: neuroendocrine tumor, primary, hepatic, metastasis, rare, neuroendocrin carcinoma,

#3755 Large cell neuroendocrine carcinoma of the breast

Introduction: Primary neuroendocrine breast carcinomas are rare and little-known tumors. They account for only 2 % to 5 % of breast cancers. Diagnosis is based on neuroendocrine architecture associated with the expression of neuroendocrine markers.

Conference:

Presenting Author:

Authors: Samia K, Siham C, Fatima H,

Keywords: large cell neuroendocrine carcinoma, neuroendocrine marker, chromogranin, synaptophysin, mastectomy,