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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,
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