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Pancreatic Neuroendocrine Tumors: an Update
Pancreatic neuroendocrine tumors (pNETs) are rare and comprise only 1–2 % of all pancreatic neoplastic disease. Although the majority of these tumors are sporadic (90 %), pNETs can arise in the setting of several different hereditary genetic syndromes, most commonly multiple endocrine neoplasia type...
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| Pubblicato in: | Indian J Surg |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer India
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4689705/ https://ncbi.nlm.nih.gov/pubmed/26722203 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12262-015-1360-2 |
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