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Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature
BACKGROUND: Recently, gastrointestinal stromal tumors that have developed outside of the digestive tract have been reported. These tumors are collectively termed extra-gastrointestinal stromal tumors. Extra-gastrointestinal stromal tumors can also develop in the liver. Only eight case reports involv...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009116/ https://www.ncbi.nlm.nih.gov/pubmed/27586264 http://dx.doi.org/10.1186/s40792-016-0218-6 |
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author | Nagai, Takeshi Ueda, Kazumitsu Hakoda, Hiroyuki Okata, Shinya Nakata, Shoko Taira, Tetsuro Aoki, Shigeo Mishima, Hideyuki Sako, Akihiro Maruyama, Tsunehiko Okumura, Minoru |
author_facet | Nagai, Takeshi Ueda, Kazumitsu Hakoda, Hiroyuki Okata, Shinya Nakata, Shoko Taira, Tetsuro Aoki, Shigeo Mishima, Hideyuki Sako, Akihiro Maruyama, Tsunehiko Okumura, Minoru |
author_sort | Nagai, Takeshi |
collection | PubMed |
description | BACKGROUND: Recently, gastrointestinal stromal tumors that have developed outside of the digestive tract have been reported. These tumors are collectively termed extra-gastrointestinal stromal tumors. Extra-gastrointestinal stromal tumors can also develop in the liver. Only eight case reports involving primary GIST of the liver have been published. We report a case and review the literature regarding this disease. CASE PRESENTATION: A 70-year-old woman with a past history of gastric cancer visited our hospital for regular inspection. With extensive radiological imaging, a computed tomography scan revealed a mass with a size of 6.8 cm in the lateral segment of the liver. (18)F-Fluoro-2-deoxyglucose positron emission tomography revealed no other malignancies except for the liver tumor. Because the lesion was suspected of being a primary malignant hepatic tumor, lateral segmentectomy was performed. The immunohistochemical analysis supported the diagnosis of gastrointestinal stromal tumors in the liver. The patient has had no evidence of recurrence during the 10-month follow-up period; imatinib chemotherapy was not administered. CONCLUSIONS: Primary hepatic gastrointestinal stromal tumors had no characteristics that distinguished them from ordinary tumors in imaging examinations. Primary gastrointestinal stromal tumors might have developed from interstitial Cajal-like cells. |
format | Online Article Text |
id | pubmed-5009116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-50091162016-09-22 Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature Nagai, Takeshi Ueda, Kazumitsu Hakoda, Hiroyuki Okata, Shinya Nakata, Shoko Taira, Tetsuro Aoki, Shigeo Mishima, Hideyuki Sako, Akihiro Maruyama, Tsunehiko Okumura, Minoru Surg Case Rep Case Report BACKGROUND: Recently, gastrointestinal stromal tumors that have developed outside of the digestive tract have been reported. These tumors are collectively termed extra-gastrointestinal stromal tumors. Extra-gastrointestinal stromal tumors can also develop in the liver. Only eight case reports involving primary GIST of the liver have been published. We report a case and review the literature regarding this disease. CASE PRESENTATION: A 70-year-old woman with a past history of gastric cancer visited our hospital for regular inspection. With extensive radiological imaging, a computed tomography scan revealed a mass with a size of 6.8 cm in the lateral segment of the liver. (18)F-Fluoro-2-deoxyglucose positron emission tomography revealed no other malignancies except for the liver tumor. Because the lesion was suspected of being a primary malignant hepatic tumor, lateral segmentectomy was performed. The immunohistochemical analysis supported the diagnosis of gastrointestinal stromal tumors in the liver. The patient has had no evidence of recurrence during the 10-month follow-up period; imatinib chemotherapy was not administered. CONCLUSIONS: Primary hepatic gastrointestinal stromal tumors had no characteristics that distinguished them from ordinary tumors in imaging examinations. Primary gastrointestinal stromal tumors might have developed from interstitial Cajal-like cells. Springer Berlin Heidelberg 2016-09-01 /pmc/articles/PMC5009116/ /pubmed/27586264 http://dx.doi.org/10.1186/s40792-016-0218-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Case Report Nagai, Takeshi Ueda, Kazumitsu Hakoda, Hiroyuki Okata, Shinya Nakata, Shoko Taira, Tetsuro Aoki, Shigeo Mishima, Hideyuki Sako, Akihiro Maruyama, Tsunehiko Okumura, Minoru Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title | Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title_full | Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title_fullStr | Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title_full_unstemmed | Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title_short | Primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
title_sort | primary gastrointestinal stromal tumor of the liver: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009116/ https://www.ncbi.nlm.nih.gov/pubmed/27586264 http://dx.doi.org/10.1186/s40792-016-0218-6 |
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