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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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| Publicado no: | J Clin Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7565036/ https://ncbi.nlm.nih.gov/pubmed/32947997 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9092993 |
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