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Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors

BACKGROUND: Neuroendocrine tumors (NETs) frequently occur in the gastrointestinal tract, lung, and pancreas, and the rectum and appendix are the sites with the highest incidence. Epidemiology statistics show that an estimated 8000 people every year in the United States are diagnosed with NETs occurr...

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Autores principales: Yu, Yong-Jun, Li, Yu-Wei, Shi, Yang, Zhang, Zhao, Zheng, Min-Ying, Zhang, Shi-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443838/
https://www.ncbi.nlm.nih.gov/pubmed/32879666
http://dx.doi.org/10.4251/wjgo.v12.i8.893
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author Yu, Yong-Jun
Li, Yu-Wei
Shi, Yang
Zhang, Zhao
Zheng, Min-Ying
Zhang, Shi-Wu
author_facet Yu, Yong-Jun
Li, Yu-Wei
Shi, Yang
Zhang, Zhao
Zheng, Min-Ying
Zhang, Shi-Wu
author_sort Yu, Yong-Jun
collection PubMed
description BACKGROUND: Neuroendocrine tumors (NETs) frequently occur in the gastrointestinal tract, lung, and pancreas, and the rectum and appendix are the sites with the highest incidence. Epidemiology statistics show that an estimated 8000 people every year in the United States are diagnosed with NETs occurring in the gastrointestinal tract, including the stomach, intestine, appendix, colon, and rectum. The pathological changes and clinical symptoms of NETs are not specific, and therefore they are frequently misdiagnosed. AIM: To investigate the clinical symptoms, pathological characteristics, treatment, and prognosis of rectal neuroendocrine tumors (RNETs) by analyzing the clinical and pathological data of 132 RNET cases at our hospital. METHODS: All RNETs were graded according to Ki-67 positivity and mitotic events. The tumors were staged as clinical stages I, II, III, and IV according to infiltrative depth and tumor size. COX proportional hazard model was used to assess the main risk factors for survival. RESULTS: These 132 RNETs included 83 cases of G1, 21 cases of G2, and 28 cases of G3 (neuroendocrine carcinoma) disease. Immunohistochemical staining showed that 89.4% of RNETs were positive for synaptophysin and 39.4% positive for chromogranin A. There were 19, 85, 23, and 5 cases of clinical stages I, II, III, and IV, respectively. The median patient age was 52.96 years. The diameter of tumor, depth of invasion, and pathological grade were the main reference factors for the treatment of RNETs. The survival rates at 6, 12, 36, and 60 mo after operation were 98.5%, 94.6%, 90.2%, and 85.6%, respectively. Gender, tumor size, tumor grade, lymph node or distant organ metastasis, and radical resection were the main factors associated with prognosis of RNETs. Multivariate analysis showed that tumor size and grade were independent prognostic factors. CONCLUSION: The clinical symptoms of RNETs are not specific, and they are easy to misdiagnose. Surgery is the main treatment method. The grade and stage of RNETs are the main indices to evaluate prognosis.
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spelling pubmed-74438382020-09-01 Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors Yu, Yong-Jun Li, Yu-Wei Shi, Yang Zhang, Zhao Zheng, Min-Ying Zhang, Shi-Wu World J Gastrointest Oncol Case Control Study BACKGROUND: Neuroendocrine tumors (NETs) frequently occur in the gastrointestinal tract, lung, and pancreas, and the rectum and appendix are the sites with the highest incidence. Epidemiology statistics show that an estimated 8000 people every year in the United States are diagnosed with NETs occurring in the gastrointestinal tract, including the stomach, intestine, appendix, colon, and rectum. The pathological changes and clinical symptoms of NETs are not specific, and therefore they are frequently misdiagnosed. AIM: To investigate the clinical symptoms, pathological characteristics, treatment, and prognosis of rectal neuroendocrine tumors (RNETs) by analyzing the clinical and pathological data of 132 RNET cases at our hospital. METHODS: All RNETs were graded according to Ki-67 positivity and mitotic events. The tumors were staged as clinical stages I, II, III, and IV according to infiltrative depth and tumor size. COX proportional hazard model was used to assess the main risk factors for survival. RESULTS: These 132 RNETs included 83 cases of G1, 21 cases of G2, and 28 cases of G3 (neuroendocrine carcinoma) disease. Immunohistochemical staining showed that 89.4% of RNETs were positive for synaptophysin and 39.4% positive for chromogranin A. There were 19, 85, 23, and 5 cases of clinical stages I, II, III, and IV, respectively. The median patient age was 52.96 years. The diameter of tumor, depth of invasion, and pathological grade were the main reference factors for the treatment of RNETs. The survival rates at 6, 12, 36, and 60 mo after operation were 98.5%, 94.6%, 90.2%, and 85.6%, respectively. Gender, tumor size, tumor grade, lymph node or distant organ metastasis, and radical resection were the main factors associated with prognosis of RNETs. Multivariate analysis showed that tumor size and grade were independent prognostic factors. CONCLUSION: The clinical symptoms of RNETs are not specific, and they are easy to misdiagnose. Surgery is the main treatment method. The grade and stage of RNETs are the main indices to evaluate prognosis. Baishideng Publishing Group Inc 2020-08-15 2020-08-15 /pmc/articles/PMC7443838/ /pubmed/32879666 http://dx.doi.org/10.4251/wjgo.v12.i8.893 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Control Study
Yu, Yong-Jun
Li, Yu-Wei
Shi, Yang
Zhang, Zhao
Zheng, Min-Ying
Zhang, Shi-Wu
Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title_full Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title_fullStr Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title_full_unstemmed Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title_short Clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
title_sort clinical and pathological characteristics and prognosis of 132 cases of rectal neuroendocrine tumors
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443838/
https://www.ncbi.nlm.nih.gov/pubmed/32879666
http://dx.doi.org/10.4251/wjgo.v12.i8.893
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