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Multiple Rectal Neuroendocrine Tumors: Report of Five Cases
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¹ÚÂù¼(Park Chan-Seo) - ¿µ³²´ëÇб³ ÀÇ°ú´ëÇÐ ³»°úÇб³½Ç
À̽ÃÇü(Lee Si-Hyung) - ¿µ³²´ëÇб³ ÀÇ°ú´ëÇÐ ³»°úÇб³½Ç
±è½Â¹ü(Kim Sung-Bum) - ¿µ³²´ëÇб³ ÀÇ°ú´ëÇÐ ³»°úÇб³½Ç
±è°æ¿Á(Kim Kyeong-Ok) - ¿µ³²´ëÇб³ ÀÇ°ú´ëÇÐ ³»°úÇб³½Ç
À庴ÀÍ(Jang Byung-Ik) - ¿µ³²´ëÇб³ ÀÇ°ú´ëÇÐ ³»°úÇб³½Ç
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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Multicentricity, Rectum, Neuroendocrine tumors
KMID :
0614620140640020103
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