Primary Neuroendocrine Neoplasm of the Anterior Sacral Region Treated by Laparoscopic Resection

Author:

Kimura Naoya1,Hiraki Masatsugu1,Koga Hiroki1,Akashi Michiaki2,Kohya Naohiko1,Samejima Ryuichiro1

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

Reference33 articles.

1. 1) Pearse AG. The cytochemistry and ultrastucture of polypeptide hormone-producing cells of the APUD series and the embryologic, physiologic and pathologic implications of the concept. J Histochem Cytochem. 1969 May;17(5):303–313.

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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