Well-differentiated pancreatic neuroendocrine tumours (PanNETs) and poorly differentiated pancreatic neuroendocrine carcinomas (PanNECs): concepts, issues and a practical diagnostic approach to high-grade (G3) cases
Author:
Affiliation:
1. Department of Pathology; University of Pittsburgh Medical Center; Pittsburgh PA USA
2. Department of Pathology; Memorial Sloan Kettering Cancer Center; New York NY USA
Publisher
Wiley
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/his.13408/fullpdf
Reference47 articles.
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2. One hundred years after ‘carcinoid’: epidemiology of and prognostic factors for neuroendocrine tumours in 35,825 cases in the United States;Yao;J. Clin. Oncol.,2008
3. Pancreatic neuroendocrine tumours (PNETs): incidence, prognosis and recent trend toward improved survival;Halfdanarson;Ann. Oncol.,2008
4. Epidemiology of gastroenteropancreatic neuroendocrine tumours;Fraenkel;Best Pract. Res. Clin. Gastroenterol.,2012
5. Consensus guidelines for the management and treatment of neuroendocrine tumours;Kunz;Pancreas,2013
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