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Article

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

European journal of gastroenterology & hepatology - 1 Aug 2014

Karakaxas Dimitrios, Gazouli Maria, Liakakos Theodoros, Vaiopoulou Anna, Apessou Dimitra, Papaparaskeva Kleo, Patapis Pavlos, Dervenis Christos

Abstract excerpt

Pancreatic neuroendocrine tumors (PNETs) share a unique genetic identity, functional behavior, and clinical course. Compared with tumors of the exocrine pancreas, they are rare and show a different biologic behavior and prognosis. On the basis of data from recent studies, all PNETs, outside of small insulinomas, should be considered potentially malignant and treated accordingly. Untreated tumors have a high...

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PMID: 24987821
DOI: 10.1097/MEG.0000000000000138

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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