Year 2016 / Volume 108 / Number 11
Editorial
Pancreas neuroendocrine tumors - not so rare or benign

687-688

DOI: 10.17235/reed.2016.4672/2016

Fernando Pereira Pérez,

Abstract
Neuroendocrine tumors (NETs) are a heterogeneous group of neoplasms characterized by a common embryonic origin and highly variable clinical outcome.
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References
1. Manual GETNE [Grupo Nacional de Tumores Neuroendocrinos] de diagnóstico y tratamiento de los tumores neuroendocrinos. ED: R. García-Carbonero, J. Aller, E. Martín, I. Sevilla. ISBN: 978-84-695-8312-8. Octubre de 2013
2. M. Falconi, B. Eriksson, G. Kaltsas et al. ENETS Consensus Guidelines Update for the Management of Patients with Functional Pancreatic Neuroendocrine Tumors and Non-Functional Pancreatic Neuroendocrine Tumors. Neuroendocrinology 2016; 103: 153–171
3. J. A. Cienfuegos, F. Rotellar F, J. Salguero et al. A single institution’s 21-year experience with surgically resected pancreatic neuroendocrine tumors: an analysis of survival and prognostic factors. REED 2016
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Publication history

Received: 12/10/2016

Accepted: 13/10/2016

Online First: 19/10/2016

Published: 02/11/2016

Article Online First time: 7 days

Article editing time: 21 days


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