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A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma
BACKGROUND: Neuroendocrine cell carcinomas (NEC) of the colon and rectum are uncommon, representing ~ 0.1% of all colorectal carcinomas. They are associated with a much worse prognosis compared to adenocarcinoma of the colon and rectum, as death occurs in approximately half of all patients within 1 ...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206053/ https://www.ncbi.nlm.nih.gov/pubmed/35713748 http://dx.doi.org/10.1186/s40792-022-01471-0 |
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author | Kobayashi, Naoya Yoshida, Hiroshi Kawaguchi, Shinya Shiraso, Satoru Nemoto, Noriko Fujikawa, Nanako Haji, Yoichi Kono, Emiko Kokubo, Shoji Tsukuda, Kazuhiko Asano, Shigeyuki Shinya, Fumiaki |
author_facet | Kobayashi, Naoya Yoshida, Hiroshi Kawaguchi, Shinya Shiraso, Satoru Nemoto, Noriko Fujikawa, Nanako Haji, Yoichi Kono, Emiko Kokubo, Shoji Tsukuda, Kazuhiko Asano, Shigeyuki Shinya, Fumiaki |
author_sort | Kobayashi, Naoya |
collection | PubMed |
description | BACKGROUND: Neuroendocrine cell carcinomas (NEC) of the colon and rectum are uncommon, representing ~ 0.1% of all colorectal carcinomas. They are associated with a much worse prognosis compared to adenocarcinoma of the colon and rectum, as death occurs in approximately half of all patients within 1 year. Lynch syndrome (LS) is the most common cause of inherited colorectal cancer, accounting for 2–4% of newly diagnosed colorectal cancer cases. This case is extremely rare which was strongly suspected LS as the background, and NEC as the histological type of colorectal cancer. CASE PRESENTATION: The patient was a 44-year-old man presenting with vomiting as the main complaint. He had undergone ileocecal resection for cecal cancer at age 29. The diagnosis was obstructive descending colorectal cancer, and colonoscopy revealed tumors in the rectum and sigmoid colon in addition. Due to multiple occurrences of colorectal cancer and its prevalence in the patient’s family, LS was suspected. The operation which was a subtotal proctocolectomy was performed. Pathological analysis revealed complete curative resection and the descending colon cancer of the obstructed portion was at the most advanced pathological Stage IIIC in UICC TNM classification, and the tissue type was a NEC. The Ki-67 index was 70%. The results of the microsatellite instability (MSI) test showed high-frequency MSI. The BRAF V600E variant was negative. The immunoexpression of MLH1 was positive, MSH2 was negative, PMS2 was positive, and MSH6 was negative. CONCLUSIONS: Extended surgery is recommended for incipient colorectal cancer in LS cases in order to reliably reduce the risk of developing metachronous colorectal cancer. The survival outcome of surgery alone on digestive tract NECs, even locoregional lesions that are completely resection, is extremely poor. It is currently unclear if digestive tract NECs develop more readily in patients with LS. The accumulation of additional cases is necessary. |
format | Online Article Text |
id | pubmed-9206053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-92060532022-06-19 A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma Kobayashi, Naoya Yoshida, Hiroshi Kawaguchi, Shinya Shiraso, Satoru Nemoto, Noriko Fujikawa, Nanako Haji, Yoichi Kono, Emiko Kokubo, Shoji Tsukuda, Kazuhiko Asano, Shigeyuki Shinya, Fumiaki Surg Case Rep Case Report BACKGROUND: Neuroendocrine cell carcinomas (NEC) of the colon and rectum are uncommon, representing ~ 0.1% of all colorectal carcinomas. They are associated with a much worse prognosis compared to adenocarcinoma of the colon and rectum, as death occurs in approximately half of all patients within 1 year. Lynch syndrome (LS) is the most common cause of inherited colorectal cancer, accounting for 2–4% of newly diagnosed colorectal cancer cases. This case is extremely rare which was strongly suspected LS as the background, and NEC as the histological type of colorectal cancer. CASE PRESENTATION: The patient was a 44-year-old man presenting with vomiting as the main complaint. He had undergone ileocecal resection for cecal cancer at age 29. The diagnosis was obstructive descending colorectal cancer, and colonoscopy revealed tumors in the rectum and sigmoid colon in addition. Due to multiple occurrences of colorectal cancer and its prevalence in the patient’s family, LS was suspected. The operation which was a subtotal proctocolectomy was performed. Pathological analysis revealed complete curative resection and the descending colon cancer of the obstructed portion was at the most advanced pathological Stage IIIC in UICC TNM classification, and the tissue type was a NEC. The Ki-67 index was 70%. The results of the microsatellite instability (MSI) test showed high-frequency MSI. The BRAF V600E variant was negative. The immunoexpression of MLH1 was positive, MSH2 was negative, PMS2 was positive, and MSH6 was negative. CONCLUSIONS: Extended surgery is recommended for incipient colorectal cancer in LS cases in order to reliably reduce the risk of developing metachronous colorectal cancer. The survival outcome of surgery alone on digestive tract NECs, even locoregional lesions that are completely resection, is extremely poor. It is currently unclear if digestive tract NECs develop more readily in patients with LS. The accumulation of additional cases is necessary. Springer Berlin Heidelberg 2022-06-17 /pmc/articles/PMC9206053/ /pubmed/35713748 http://dx.doi.org/10.1186/s40792-022-01471-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Kobayashi, Naoya Yoshida, Hiroshi Kawaguchi, Shinya Shiraso, Satoru Nemoto, Noriko Fujikawa, Nanako Haji, Yoichi Kono, Emiko Kokubo, Shoji Tsukuda, Kazuhiko Asano, Shigeyuki Shinya, Fumiaki A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title | A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title_full | A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title_fullStr | A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title_full_unstemmed | A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title_short | A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma |
title_sort | case of strongly suspected lynch syndrome with colorectal neuroendocrine carcinoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206053/ https://www.ncbi.nlm.nih.gov/pubmed/35713748 http://dx.doi.org/10.1186/s40792-022-01471-0 |
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