The genetic alterations of rectal neuroendocrine tumor and indications for therapy and prognosis: a systematic review
Author:
Affiliation:
1. Department of Endocrinology, Shunyi Hospital, Beijing Traditional Chinese Medicine Hospital, Beijing 101300, China
2. Department of Endocrinology, Fangshan Hospital Beijing University of Chinese Medicine, Beijing 102400, China
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/70/2/70_EJ22-0262/_pdf
Reference73 articles.
1. 1 Yao JC, Hassan M, Phan A, Dagohoy C, Leary C, 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: 3063–3072.
2. 2 Wang AY, Ahmad NA (2006) Rectal carcinoids. Curr Opin Gastroenterol 22: 529–535.
3. 3 Ito T, Sasano H, Tanaka M, Osamura RY, Sasaki I, et al. (2010) Epidemiological study of gastroenteropancreatic neuroendocrine tumors in Japan. J Gastroenterol 45: 234–243.
4. 4 Lim T, Lee J, Kim JJ, Lee JK, Lee KT, et al. (2011) Gastroenteropancreatic neuroendocrine tumors: incidence and treatment outcome in a single institution in Korea. Asia Pac J Clin Oncol 7: 293–299.
5. 5 Volante M, Grillo F, Massa F, Maletta F, Mastracci L, et al. (2021) Neuroendocrine neoplasms of the appendix, colon and rectum. Pathologica 113: 19–27.
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1. Laparoscopic versus open surgery for rectal neuroendocrine tumors: a multicenter real-world study;BMC Cancer;2024-08-05
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