Primary Neuroendocrine Neoplasm of the Anterior Sacral Region Treated by Laparoscopic Resection
Author:
Affiliation:
1. Department of Surgery, Karatsu Red Cross Hospital
2. Department of Pathology, Karatsu Red Cross Hospital
Publisher
The Japanese Journal of Gastroenterological Surgery
Subject
Gastroenterology,Surgery
Link
https://www.jstage.jst.go.jp/article/jjgs/56/1/56_2021.0151/_pdf
Reference33 articles.
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2. 2) 日本神経内分泌腫瘍研究会(JNETS)膵・消化管神経内分泌腫瘍診療ガイドライン第2版作成委員会編.膵・消化管神経内分泌腫瘍(NEN)ガイドライン 第2版.東京:金原出版;2019. p. 15–16.
3. 3) Hallet J, Law CH, Cukier M, Saskin R, Liu N, Singh S. Exploring the rising incidence of neuroendocrine tumors: a population-based analysis of epidemiology, metastatic presentation, and outcomes. Cancer. 2015 Feb;121(4):589–597.
4. 4) Yao JC, Hassan M, Phan A, Dagohoy C, Leary C, Mares JE, et al. One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States. J Clin Oncol. 2008 Jun;26(18):3063–3072.
5. 5) Klimstra DS, Klöppel G, La Rosa S. Classification of neuroendocrine neoplasms of the digestive system. In: WHO Classification of Tumors Editorial Board, editors. WHO classifications of tumours. 5th ed. Vol. 1. digestive system tumors. Lyon: World Health Organaization; 2019. p. 16–21.
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