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10.3748/wjg.v22.i11.3105

http://scihub22266oqcxt.onion/10.3748/wjg.v22.i11.3105
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C4789986!4789986!27003988
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suck abstract from ncbi


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pmid27003988      World+J+Gastroenterol 2016 ; 22 (11): 3105-16
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  • Multidisciplinary management of nonfunctional neuroendocrine tumor of the pancreas #MMPMID27003988
  • Folkert IW; Hernandez P; Roses RE
  • World J Gastroenterol 2016[Mar]; 22 (11): 3105-16 PMID27003988show ga
  • Pancreatic neuroendocrine tumors (PNETs) are a rare and diverse group of tumors; nonfunctional (NF) PNETs account for the majority of cases. Most patients with NF-PNETs have metastatic disease at the time of presentation. A variety of treatment modalities exist, including medical, liver directed, and surgical treatments. Aggressive surgical management is associated with prolonged survival, however available data are limited by selection bias and the frequent combination of PNETs with carcinoid tumors. Although few patients with metastatic disease will be cured, application of currently available therapies in a multidisciplinary setting can lead to excellent outcomes with prolonged patient survival.
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