Literature DB >> 25168053

Multiple rectal neuroendocrine tumors: report of five cases.

Chan Seo Park1, Si Hyung Lee, Sung Bum Kim, Kyeong Ok Kim, Byung Ik Jang.   

Abstract

Carcinoids are slow growing neuroendocrine tumors (NET) originating in the enterochromaffin cells of the gastrointestinal tract. In previous studies, rectal NET comprised only about 1% of all anorectal neoplasms; however, the incidence of rectal NET has shown a recent increase. Typically, rectal NET presents as a single subepithelial nodule, and multicentricity of rectal NETs is rare, with reported incidence of 2-4.5%. Due to the rarity of multiple rectal NETs, there is no consensus or guidelines for treatment of multiple rectal NETs. However, NETs of the rectum that are less than 10 mm in diameter and do not infiltrate the muscularis propria, without distant metastasis, can be removed by endoscopy, as with solitary rectal NET. We encountered five cases of multiple rectal NETs which were treated successfully by endoscopy.

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Year:  2014        PMID: 25168053     DOI: 10.4166/kjg.2014.64.2.103

Source DB:  PubMed          Journal:  Korean J Gastroenterol        ISSN: 1598-9992


  2 in total

Review 1.  Neurofibromatosis type 1-associated multiple rectal neuroendocrine tumors: A case report and review of the literature.

Authors:  Rui Xie; Kuang-I Fu; Shao-Min Chen; Bi-Guang Tuo; Hui-Chao Wu
Journal:  World J Gastroenterol       Date:  2018-09-07       Impact factor: 5.742

2.  Multiple rectal neuroendocrine tumors: An analysis of 15 cases and literature review.

Authors:  Shu Pang; Ye Zong; Kun Zhang; Haiying Zhao; Yongjun Wang; Junxiong Wang; Chuntao Liu; Yongdong Wu; Peng Li
Journal:  Front Oncol       Date:  2022-09-14       Impact factor: 5.738

  2 in total

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