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Introduction: Pancreatic neuroendocrine tumors (PNET) are rare, heterogeneous and challenging neoplasms. Surgical resection is the only curative treatment. Recurrence can occur even after years. Diagnosis of malignancy is difficult so further studies are necessary to identify prognostic criteria.
Conference: 15th Annual ENETSConcerence (2018)
Presenting Author:
Authors: Blanco L, Dopazo C, Pando E, Caralt M, Puértolas N,
Introduction: Pancreatic neuroendocrine tumors (PNETs) represent only 1% of all pancreatic neoplasms by incidence, but 10% by prevalence. Family history of cancer is the only established risk factor so far. The impact of germline genetic variability on PNET risk is poorly understood.
Conference: 12th Annual ENETSConcerence (2015)
Presenting Author: Canzian F
Authors: Campa D, Rizzato C, Capurso G, Delle Fave G, Gazouli M,
Keywords: pancreatic neuroendocrine tumor, p16, cdkn2a, genetic polymorphisms, SNP, association, susceptibility,
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