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Pancreatic neuroendocrine tumor accompanied with multiple liver metastases
Pancreatic neuroendocrine tumor (P-NET) is rare and slow-growing. Current classifications predict its prognosis and postoperative recurrence. Curative resection is ideal, although often difficult, because over 80% of patients have unresectable multiple liver metastases and extrahepatic metastasis. A...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Baishideng Publishing Group Inc
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4163742/ https://ncbi.nlm.nih.gov/pubmed/25232452 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4254/wjh.v6.i8.596 |
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