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Kulke MH , Benson AB , Bergsland E , Berlin JD , Blaszkowsky LS , Choti MA , Clark OH , Doherty GM , Eason J , Emerson L , Engstrom PF , Goldner WS , Heslin MJ , Kandeel F , Kunz PL , Kuvshinoff BW , Moley JF , Pillarisetty VG , Saltz L , Schteingart DE , Shah MH , Shibata S , Strosberg JR , Vauthey JN , White R , Yao JC , Freedman-Cass DA , Dwyer MA
Neuroendocrine Tumors Clinical Practice Guidelines in Oncology
Journal of the National Comprehensive Cancer Network. 2012 Jun;10(6) :724-764
PMID: WOS:000304889700006   
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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. (JNCCN 2012;10:724-764)
Notes
Kulke, Matthew H. Benson, Al B., III Bergsland, Emily Berlin, Jordan D. Blaszkowsky, Lawrence S. Choti, Michael A. Clark, Orlo H. Doherty, Gerard M. Eason, James Emerson, Lyska Engstrom, Paul F. Goldner, Whitney S. Heslin, Martin J. Kandeel, Fouad Kunz, Pamela L. Kuvshinoff, Boris W., II Moley, Jeffrey F. Pillarisetty, Venu G. Saltz, Leonard Schteingart, David E. Shah, Manisha H. Shibata, Stephen Strosberg, Jonathan R. Vauthey, Jean-Nicolas White, Rebekah Yao, James C. Freedman-Cass, Deborah A. Dwyer, Mary A. 157 Harborside press Cold spring harbor 953rf Rtagna c, 1981, american journal of medicine, v71, p855