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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...

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Autores principales: Wen, Jun, Zhao, Wei, Li, Chuan, Shen, Jun-Yi, Wen, Tian-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
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.
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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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