Surgical Management of Neuroendocrine Tumours of the Pancreas

Neuroendocrine tumours of the pancreas (pNET) are rare, accounting for 1–2% of all pancreatic neoplasms. They develop from pancreatic islet cells and cover a wide range of heterogeneous neoplasms. While most pNETs are sporadic, some are associated with genetic syndromes. Furthermore, some pNETs are...

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Detalles Bibliográficos
Autores principales: Souche, Regis, Hobeika, Christian, Hain, Elisabeth, Gaujoux, Sebastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565036/
https://www.ncbi.nlm.nih.gov/pubmed/32947997
http://dx.doi.org/10.3390/jcm9092993

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565036/
https://www.ncbi.nlm.nih.gov/pubmed/32947997
http://dx.doi.org/10.3390/jcm9092993

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