A Case of Pancreatic Neuroendocrine Tumor G3 Which Responded Remarkably to Chemotherapy
Author:
Affiliation:
1. Third Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan.
2. Department of Pathology and Cell Biology, School of Medicine, University of Occupational and Environmental Health, Japan.
Publisher
The University of Occupational and Environmental Health, Japan
Subject
Public Health, Environmental and Occupational Health,General Medicine
Link
https://www.jstage.jst.go.jp/article/juoeh/44/3/44_287/_pdf
Reference20 articles.
1. 1 . Schimmack S, Svejda B, Lawrence B, Kidd M & Modlin IM (2011): The diversity and commonalities of gastroenteropancreatic neuroendocrine tumors. Langenbecks Arch Surg 396 (3): 273−298
2. 2 . Ito T, Igarashi H, Nakamura K et al (2015): Epidemiological trends of pancreatic and gastrointestinal neuroendocrine tumors in Japan: a nationwide survey analysis. J Gastroenterol 50 (1): 58−64
3. 3 . Yao JC, Hassan M, Phan A et al (2008): One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States. J Clin Oncol 26 (18): 3063−3072
4. 4 . Bosman FT, World Health Organization & International Agency for Research on Cancer (2010): WHO classification of tumours of the digestive system. 4th ed. International Agency for Research on Cancer, Lyon 417pp
5. 5 . Lloyd RV, Osamura RY, Klöppel G & Rosai J (2017): WHO classification of tumours of endocrine organs. 4th ed ed. International Agency for Research on Cancer, Lyon 355pp
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