Abstract Library
Welcome to the open-access search for all ENETS abstracts presented at the Annual ENETS Conferences.
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ENETS Abstract Search
Introduction: Meckel’s diverticulum is a rare finding in adults but can harbour malignancies such as leiomyosarcoma or neuroendocrine tumours (NET). The clinical presentation and tumour characteristics, including grading, have shown high variability in recent studies for NET.
Conference:
Presenting Author: Berckenhagen L
Authors: Berckenhagen L, Weidemann S, Amin T, Ritter A, Poppinga J,
Keywords: Meckel’s diverticula, incidental NET, acute abdomen, lower GI-bleeding,
#4614 Rare diagnosis of intrapancreatic accessory spleen mimicking PanNET
Introduction: A 44-year-old woman with hypertension and an autoimmune thyroid disease. With a positive family history of pancreatic and oesophageal cancer. Referred to our clinic for an incidental finding of a tumour in the tail of the pancreas on abdominal ultrasound by a surgeon.
Conference:
Presenting Author: Uhrík P
Authors: Uhrík P, Nosakova L, Vojtko M, Bánovčin P,
Keywords: fine needle biopsy, accessory spleen, Neuroendocrine tumour,
#4525 MRI findings of jejunal mesentery neuroendocrine tumour – A case report
Introduction: Neuroendocrine tumours arising from the mesentery are uncommon, with corresponding MRI features infrequently documented in the literature.
Conference:
Presenting Author:
Authors: Guo L, Li Z, Yang H, Dong H, Wang Y,
Keywords: Magnetic Resonance Imaging, Jejunal Mesentery, Neuroendocrine Tumour, Diagnosis,
Introduction: Grade I neuroendocrine tumours (NETs) represent a distinct clinico-histological entity that requires a tailored management approach. The treatment of these tumours has evolved, but challenges remain, especially in regions with limited access to nuclear medicine imaging.
Conference:
Presenting Author:
Authors: Boudersa A, Kouadri N, Bouguettaya A,
#4449 Treatment of MiNEN with peptide receptor radionuclide therapy
Introduction: Mixed non-neuroendocrine and neuroendocrine neoplasms (MiNENs) of gastrointestinal tract are rare tumours with characteristic histological features include at least 30% of both neuroendocrine and non-neuroendocrine components of the whole neoplasm. They are usually treated with surgical resection and chemotherapy in advanced disease. However, there is scarcity of data for the use of peptide receptor radionuclide therapy (PRRT) in these tumours.
Conference:
Presenting Author: Shekhda K
Authors: Shekhda K, Luong T, Paterson A, Navalkissoor S, Krell D,