| Literature DB >> 25583772 |
Matthew H Kulke, Manisha H Shah, Al B Benson, Emily Bergsland, Jordan D Berlin, Lawrence S Blaszkowsky, Lyska Emerson, Paul F Engstrom, Paul Fanta, Thomas Giordano, Whitney S Goldner, Thorvardur R Halfdanarson, Martin J Heslin, Fouad Kandeel, Pamela L Kunz, Boris W Kuvshinoff, Christopher Lieu, Jeffrey F Moley, Gitonga Munene, Venu G Pillarisetty, Leonard Saltz, Julie Ann Sosa, Jonathan R Strosberg, Jean-Nicolas Vauthey, Christopher Wolfgang, James C Yao, Jennifer Burns, Deborah Freedman-Cass.
Abstract
Neuroendocrine tumors (NETs) comprise a broad family of tumors that may or may not be associated with symptoms attributable to hormonal hypersecretion. The NCCN Clinical Practice Guidelines in Oncology for Neuroendocrine Tumors discuss the diagnosis and management of both sporadic and hereditary NETs. This selection from the guidelines focuses on sporadic NETs of the pancreas, gastrointestinal tract, lung, and thymus.Entities:
Mesh：
Year: 2015 PMID： 25583772 DOI： 10.6004/jnccn.2015.0011
Source DB: PubMed Journal: J Natl Compr Canc Netw ISSN： 1540-1405 Impact factor: 11.908