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Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report
BACKGROUND: Carcinoma of the ampulla of Vater is an uncommon ampullo-pancreatobiliary neoplasm, and the most common histological type is adenocarcinoma with a tubular growth pattern. Invasive micropapillary carcinoma (IMPC) is an aggressive variant of adenocarcinoma in several organs that is associa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040169/ https://www.ncbi.nlm.nih.gov/pubmed/33889635 http://dx.doi.org/10.12998/wjcc.v9.i11.2671 |
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author | Noguchi, Hirotsugu Higashi, Michiyo Idichi, Tetsuya Kurahara, Hiroshi Mataki, Yuko Tasaki, Takashi Kitazono, Ikumi Ohtsuka, Takao Tanimoto, Akihide |
author_facet | Noguchi, Hirotsugu Higashi, Michiyo Idichi, Tetsuya Kurahara, Hiroshi Mataki, Yuko Tasaki, Takashi Kitazono, Ikumi Ohtsuka, Takao Tanimoto, Akihide |
author_sort | Noguchi, Hirotsugu |
collection | PubMed |
description | BACKGROUND: Carcinoma of the ampulla of Vater is an uncommon ampullo-pancreatobiliary neoplasm, and the most common histological type is adenocarcinoma with a tubular growth pattern. Invasive micropapillary carcinoma (IMPC) is an aggressive variant of adenocarcinoma in several organs that is associated with lymph node metastasis and poor prognosis. IMPC was first described as a histological subtype of breast cancer; however, IMPC of the ampulla of Vater is extremely rare, with only three articles reported in the English literature. CASE SUMMARY: We have reported a case of IMPC of the ampulla of Vater in an 80-year-old man. Microscopically, the surface area of the carcinoma was composed of tubulopapillary structures mimicking intra-ampullary papillary-tubular neoplasm, and the deep invasive front area exhibited a pattern of IMPC. The carcinoma showed lymphatic invasion and extensive lymph node metastasis. The immunohistochemical study revealed mixed intestinal and gastric/pan-creatobiliary phenotypes. CONCLUSION: This rare subtype tumor in the ampulla of Vater showed a histologically mixed phenotype and exhibited aggressive behavior. |
format | Online Article Text |
id | pubmed-8040169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-80401692021-04-21 Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report Noguchi, Hirotsugu Higashi, Michiyo Idichi, Tetsuya Kurahara, Hiroshi Mataki, Yuko Tasaki, Takashi Kitazono, Ikumi Ohtsuka, Takao Tanimoto, Akihide World J Clin Cases Case Report BACKGROUND: Carcinoma of the ampulla of Vater is an uncommon ampullo-pancreatobiliary neoplasm, and the most common histological type is adenocarcinoma with a tubular growth pattern. Invasive micropapillary carcinoma (IMPC) is an aggressive variant of adenocarcinoma in several organs that is associated with lymph node metastasis and poor prognosis. IMPC was first described as a histological subtype of breast cancer; however, IMPC of the ampulla of Vater is extremely rare, with only three articles reported in the English literature. CASE SUMMARY: We have reported a case of IMPC of the ampulla of Vater in an 80-year-old man. Microscopically, the surface area of the carcinoma was composed of tubulopapillary structures mimicking intra-ampullary papillary-tubular neoplasm, and the deep invasive front area exhibited a pattern of IMPC. The carcinoma showed lymphatic invasion and extensive lymph node metastasis. The immunohistochemical study revealed mixed intestinal and gastric/pan-creatobiliary phenotypes. CONCLUSION: This rare subtype tumor in the ampulla of Vater showed a histologically mixed phenotype and exhibited aggressive behavior. Baishideng Publishing Group Inc 2021-04-16 2021-04-16 /pmc/articles/PMC8040169/ /pubmed/33889635 http://dx.doi.org/10.12998/wjcc.v9.i11.2671 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://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. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Noguchi, Hirotsugu Higashi, Michiyo Idichi, Tetsuya Kurahara, Hiroshi Mataki, Yuko Tasaki, Takashi Kitazono, Ikumi Ohtsuka, Takao Tanimoto, Akihide Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title | Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title_full | Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title_fullStr | Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title_full_unstemmed | Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title_short | Rare histological subtype of invasive micropapillary carcinoma in the ampulla of Vater: A case report |
title_sort | rare histological subtype of invasive micropapillary carcinoma in the ampulla of vater: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040169/ https://www.ncbi.nlm.nih.gov/pubmed/33889635 http://dx.doi.org/10.12998/wjcc.v9.i11.2671 |
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