| Literature DB >> 22679117 |
Matthew H Kulke1, Al B Benson, Emily Bergsland, Jordan D Berlin, Lawrence S Blaszkowsky, Michael A Choti, Orlo H Clark, Gerard M Doherty, James Eason, Lyska Emerson, Paul F Engstrom, Whitney S Goldner, Martin J Heslin, Fouad Kandeel, Pamela L Kunz, Boris W Kuvshinoff, Jeffrey F Moley, Venu G Pillarisetty, Leonard Saltz, David E Schteingart, Manisha H Shah, Stephen Shibata, Jonathan R Strosberg, Jean-Nicolas Vauthey, Rebekah White, James C Yao, Deborah A Freedman-Cass, Mary A Dwyer.
Abstract
Neuroendocrine tumors comprise a broad family of tumors, the most common of which are carcinoid and pancreatic neuroendocrine tumors. The NCCN Neuroendocrine Tumors Guidelines discuss the diagnosis and management of both sporadic and hereditary neuroendocrine tumors. Most of the recommendations pertain to well-differentiated, low- to intermediate-grade tumors. This updated version of the NCCN Guidelines includes a new section on pathology for diagnosis and reporting and revised recommendations for the surgical management of neuroendocrine tumors of the pancreas.Entities:
Mesh：
Year: 2012 PMID： 22679117 DOI： 10.6004/jnccn.2012.0075
Source DB: PubMed Journal: J Natl Compr Canc Netw ISSN： 1540-1405 Impact factor: 11.908