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High-grade myofibroblastic sarcoma in the liver: A case report
Only two cases of myofibroblastic sarcoma in the liver have been reported in the literature. Here, we report the case of a male patient with high-grade myofibroblastic sarcoma mimicking echinococcosis in the liver. The 25-year-old male patient complained of right upper quadrant swelling pain for one...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658323/ https://www.ncbi.nlm.nih.gov/pubmed/29097878 http://dx.doi.org/10.3748/wjg.v23.i38.7054 |
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author | Wen, Jun Zhao, Wei Li, Chuan Shen, Jun-Yi Wen, Tian-Fu |
author_facet | Wen, Jun Zhao, Wei Li, Chuan Shen, Jun-Yi Wen, Tian-Fu |
author_sort | Wen, Jun |
collection | PubMed |
description | Only two cases of myofibroblastic sarcoma in the liver have been reported in the literature. Here, we report the case of a male patient with high-grade myofibroblastic sarcoma mimicking echinococcosis in the liver. The 25-year-old male patient complained of right upper quadrant swelling pain for one week and was initially diagnosed with echinococcosis. He was then scheduled for an exploratory laparotomy. During the operation, a huge mass exceeding 16 cm in diameter was found to occupy nearly the entire right trisegment of the liver, with a clear boundary and a round shape, and the mass was resected by right hepatic trisegmentectomy. Immunohistochemical staining revealed that the tumor tissue was positive for desmin, α-smooth muscle actin, CD56, and vimentin and negative for ALK-1, myogenin, calponin, β-catenin, S100, and glypican-3, with a Ki-67 (MIB-1) index of approximately 20%. Based on the histological manifestations and immunohistochemical staining, a diagnosis of myofibroblastic sarcoma was established. The postoperative recovery was uneventful. There was no evidence of recurrence or metastasis through the last follow-up, 6 mo after surgery, despite a lack of postoperative chemotherapy or radiotherapy. To the best of our knowledge, the present case is the first reported case of high-grade myofibroblastic sarcoma in the liver, and it is also the first reported case in a male patient. |
format | Online Article Text |
id | pubmed-5658323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-56583232017-11-02 High-grade myofibroblastic sarcoma in the liver: A case report Wen, Jun Zhao, Wei Li, Chuan Shen, Jun-Yi Wen, Tian-Fu World J Gastroenterol Case Report Only two cases of myofibroblastic sarcoma in the liver have been reported in the literature. Here, we report the case of a male patient with high-grade myofibroblastic sarcoma mimicking echinococcosis in the liver. The 25-year-old male patient complained of right upper quadrant swelling pain for one week and was initially diagnosed with echinococcosis. He was then scheduled for an exploratory laparotomy. During the operation, a huge mass exceeding 16 cm in diameter was found to occupy nearly the entire right trisegment of the liver, with a clear boundary and a round shape, and the mass was resected by right hepatic trisegmentectomy. Immunohistochemical staining revealed that the tumor tissue was positive for desmin, α-smooth muscle actin, CD56, and vimentin and negative for ALK-1, myogenin, calponin, β-catenin, S100, and glypican-3, with a Ki-67 (MIB-1) index of approximately 20%. Based on the histological manifestations and immunohistochemical staining, a diagnosis of myofibroblastic sarcoma was established. The postoperative recovery was uneventful. There was no evidence of recurrence or metastasis through the last follow-up, 6 mo after surgery, despite a lack of postoperative chemotherapy or radiotherapy. To the best of our knowledge, the present case is the first reported case of high-grade myofibroblastic sarcoma in the liver, and it is also the first reported case in a male patient. Baishideng Publishing Group Inc 2017-10-14 2017-10-14 /pmc/articles/PMC5658323/ /pubmed/29097878 http://dx.doi.org/10.3748/wjg.v23.i38.7054 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (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 Report Wen, Jun Zhao, Wei Li, Chuan Shen, Jun-Yi Wen, Tian-Fu High-grade myofibroblastic sarcoma in the liver: A case report |
title | High-grade myofibroblastic sarcoma in the liver: A case report |
title_full | High-grade myofibroblastic sarcoma in the liver: A case report |
title_fullStr | High-grade myofibroblastic sarcoma in the liver: A case report |
title_full_unstemmed | High-grade myofibroblastic sarcoma in the liver: A case report |
title_short | High-grade myofibroblastic sarcoma in the liver: A case report |
title_sort | high-grade myofibroblastic sarcoma in the liver: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658323/ https://www.ncbi.nlm.nih.gov/pubmed/29097878 http://dx.doi.org/10.3748/wjg.v23.i38.7054 |
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