Pancreatic neuroendocrine tumors: current opinions on a rare, but potentially curable neoplasm

D Karakaxas, M Gazouli, T Liakakos… - European Journal of …, 2014 - journals.lww.com
Pancreatic neuroendocrine tumors (PNETs) share a unique genetic identity, functional
behavior, and clinical course. Compared with tumors of the exocrine pancreas, they are rare …

Molecular profiling of pancreatic neuroendocrine tumors (pNETS) and the clinical potential

M Camilli, K Papadimitriou, A Nogueira… - Expert review of …, 2018 - Taylor & Francis
Introduction: Pancreatic neuroendocrine tumors (pNETs) represent a small part of pancreatic
neoplasms, and the knowledge about their indolent clinical course remains a subject of …

[HTML][HTML] Pancreatic neuroendocrine tumors: biology, diagnosis, and treatment

C Ro, W Chai, EY Victoria, R Yu - Chinese journal of cancer, 2013 - ncbi.nlm.nih.gov
Pancreatic neuroendocrine tumors (PNETs), a group of endocrine tumors arising in the
pancreas, are among the most common neuroendocrine tumors. The genetic causes of …

Molecular pathogenesis and targeted therapy of sporadic pancreatic neuroendocrine tumors

G Capurso, L Archibugi… - Journal of Hepato‐Biliary …, 2015 - Wiley Online Library
Over the past few years, knowledge regarding the molecular pathology of sporadic
pancreatic neuroendocrine tumors (PNETs) has increased substantially, and a number of …

[PDF][PDF] Neuroendocrine tumors of the pancreas: molecular pathogenesis and current surgical management

TC Lairmore, CE Quinn… - Transl. Gastrointest …, 2014 - cdn.amegroups.cn
Neuroendocrine tumors (NET) of the pancreas are uncommon neoplasms that arise from the
pancreatic islet cells. The clinical presentation of specific tumors is characterized by unique …

Pancreatic neuroendocrine tumors

E Batcher, P Madaj, AG Gianoukakis - Endocrine research, 2011 - Taylor & Francis
Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms representing< 5% of all
pancreatic malignancies with an estimated incidence of 1–1.5 cases/100,000. PNETs are …

[引用][C] Pancreas neuroendocrine tumors-not so rare or benign

FP Pérez - Revista espanola de enfermedades digestivas, 2016 - pubmed.ncbi.nlm.nih.gov
Neuroendocrine tumors (NETs) are a heterogeneous group of neoplasms characterized by
a common embryonic origin and highly variable clinical outcome.

Pancreatic neuroendocrine tumors: an update

A Paniccia, BH Edil, RD Schulick - Indian Journal of Surgery, 2015 - Springer
Pancreatic neuroendocrine tumors (pNETs) are rare and comprise only 1–2% of all
pancreatic neoplastic disease. Although the majority of these tumors are sporadic (90%) …

[HTML][HTML] Update on pancreatic neuroendocrine tumors

LR McKenna, BH Edil - Gland surgery, 2014 - ncbi.nlm.nih.gov
Pancreatic neuroendocrine tumors (pNETs) are relatively rare tumors comprising 1-2% of all
pancreas neoplasms. In the last 10 years our understanding of this disease has increased …

Surgical management of neuroendocrine tumours of the pancreas

R Souche, C Hobeika, E Hain, S Gaujoux - Journal of Clinical Medicine, 2020 - mdpi.com
Neuroendocrine tumours of the pancreas (pNET) are rare, accounting for 1–2% of all
pancreatic neoplasms. They develop from pancreatic islet cells and cover a wide range of …