Surgical Treatment of Sporadic Pancreatic Neuroendocrine Tumors: A State of the Art Review

Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms. They are clinically diverse and divided into functioning and nonfunctioning disease, depending on their ability to produce symptoms due to hormone production. Surgical resection is the only curative treatment and remains the cornerstone th...

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Detalles Bibliográficos
Autores principales: Haugvik, Sven-Petter, Labori, Knut Jørgen, Edwin, Bjørn, Mathisen, Øystein, Gladhaug, Ivar Prydz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific World Journal 2012
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523601/
https://www.ncbi.nlm.nih.gov/pubmed/23304085
http://dx.doi.org/10.1100/2012/357475

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523601/
https://www.ncbi.nlm.nih.gov/pubmed/23304085
http://dx.doi.org/10.1100/2012/357475

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