Year 2017 / Volume 109 / Number 6
Letter to the Editor
Pancreatic neuroendocrine tumors

480-481

DOI: 10.17235/reed.2017.4725/2016

Modesto Varas Lorenzo, Esteban Cugat Andorra, Jaume Capdevila Castillón,

Abstract
Endocrine or pancreatic neuroendocrine tumors (PNET) were first cited in the 1950s; they may be sporadic or associated with hereditary syndromes, benign or malignant, functioning or non-functioning. Nowadays, NF-PNETs are the most frequent and their prevalence ranges from 50% to 91%. In our current series (including 70 cases, 33% malignant, 52 operated) the frequency was 72% as compared to 37% in the historical series.
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References
Bibliografía:
1. Varas M, Gornals J, Ponseti J.Mª, et al. Tumores endocrinos o apudomas pancreáticos. Rev Esp Enferm Dig 2011; 103: 184-190.
2. Cienfuegos JA, Rotellar F, Salguero J, et al. A single institution´s 21-year experience with surgically resected pancreatic neuroendocrine tumors: an anlysis of survival and prognostic factors. Rev Esp Enferm Dig 2016; 108: 689-96.
3. Gornals J, Varas M, Catalá I, et al. Diagnóstico definitivo de los tumores neuroendocrinos (TNE) mediante PAAF ecodirigida por ultrasonografía endoscópica (USE). Rev Esp Enferm Dig 2011; 103: 123-128.
4. Alventosa C, Ferrer L, Huguet JM, et al. Síndrome de Zollinger-Ellison. Rev Esp Enferm Dig 2013; 105: 640-2.
5. Chheda Y, Arora D, Patel R, et al. A retrospective analysis of neuroendocrine tumour of páncreas: a single institute study. Intern J Res Med Sci 2015; 3: 3041-45.
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Varas Lorenzo M, Cugat Andorra E, Capdevila Castillón J. Pancreatic neuroendocrine tumors. 4725/2016


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Publication history

Received: 12/11/2016

Accepted: 18/11/2016

Online First: 03/03/2017

Published: 01/06/2017

Article Online First time: 111 days

Article editing time: 201 days


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