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Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report
BACKGROUND: Myxofibrosarcoma (MFS) is a fibroblast-derived sarcoma that mainly occurs in subcutaneous tissue. MFS rarely occurs in the gastrointestinal tract, especially in the esophagus. CASE SUMMARY: A 79-year-old male patient was admitted to our hospital for dysphagia for a week. Computed tomogra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979301/ https://www.ncbi.nlm.nih.gov/pubmed/36874423 http://dx.doi.org/10.12998/wjcc.v11.i5.1094 |
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author | Wang, Xiao-Song Zhao, Cheng-Guang Wang, Hui-Ming Wang, Xiao-Yan |
author_facet | Wang, Xiao-Song Zhao, Cheng-Guang Wang, Hui-Ming Wang, Xiao-Yan |
author_sort | Wang, Xiao-Song |
collection | PubMed |
description | BACKGROUND: Myxofibrosarcoma (MFS) is a fibroblast-derived sarcoma that mainly occurs in subcutaneous tissue. MFS rarely occurs in the gastrointestinal tract, especially in the esophagus. CASE SUMMARY: A 79-year-old male patient was admitted to our hospital for dysphagia for a week. Computed tomography and electronic gastroscopy showed that a giant mass was located 30 cm from the incisor and extended to the cardia. There was incomplete esophageal stenosis. Endoscopic pathology showed spindle cell lesions, which were considered inflammatory myofibroblast like hyperplasia. Considering the strong demands of the patient and his family, and the fact that most inflammatory myofibroblast tumors are benign, we decided to perform endoscopic submucosal dissection (ESD) even if the tumor size was giant (9.0 cm × 3.0 cm). Postoperative pathological examination resulted in a final diagnosis of MFS. MFS rarely occurs in the gastrointestinal tract, especially in the esophagus. Surgical resection and local adjuvant radiotherapy are the first choices to improve the prognosis. This case report firstly described the ESD for esophageal giant MFS. It suggests that ESD may be an alternative treatment for primary esophageal MFS. CONCLUSION: This case report for the first time describe the successful treatment of a giant esophageal MFS by ESD, suggesting that ESD may be an alternative treatment for primary esophageal MFS, especially in elderly high-risk patients with obvious dysphagia symptoms. |
format | Online Article Text |
id | pubmed-9979301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-99793012023-03-03 Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report Wang, Xiao-Song Zhao, Cheng-Guang Wang, Hui-Ming Wang, Xiao-Yan World J Clin Cases Case Report BACKGROUND: Myxofibrosarcoma (MFS) is a fibroblast-derived sarcoma that mainly occurs in subcutaneous tissue. MFS rarely occurs in the gastrointestinal tract, especially in the esophagus. CASE SUMMARY: A 79-year-old male patient was admitted to our hospital for dysphagia for a week. Computed tomography and electronic gastroscopy showed that a giant mass was located 30 cm from the incisor and extended to the cardia. There was incomplete esophageal stenosis. Endoscopic pathology showed spindle cell lesions, which were considered inflammatory myofibroblast like hyperplasia. Considering the strong demands of the patient and his family, and the fact that most inflammatory myofibroblast tumors are benign, we decided to perform endoscopic submucosal dissection (ESD) even if the tumor size was giant (9.0 cm × 3.0 cm). Postoperative pathological examination resulted in a final diagnosis of MFS. MFS rarely occurs in the gastrointestinal tract, especially in the esophagus. Surgical resection and local adjuvant radiotherapy are the first choices to improve the prognosis. This case report firstly described the ESD for esophageal giant MFS. It suggests that ESD may be an alternative treatment for primary esophageal MFS. CONCLUSION: This case report for the first time describe the successful treatment of a giant esophageal MFS by ESD, suggesting that ESD may be an alternative treatment for primary esophageal MFS, especially in elderly high-risk patients with obvious dysphagia symptoms. Baishideng Publishing Group Inc 2023-02-16 2023-02-16 /pmc/articles/PMC9979301/ /pubmed/36874423 http://dx.doi.org/10.12998/wjcc.v11.i5.1094 Text en ©The Author(s) 2023. 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. |
spellingShingle | Case Report Wang, Xiao-Song Zhao, Cheng-Guang Wang, Hui-Ming Wang, Xiao-Yan Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title | Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title_full | Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title_fullStr | Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title_full_unstemmed | Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title_short | Giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: A case report |
title_sort | giant myxofibrosarcoma of the esophagus treated by endoscopic submucosal dissection: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979301/ https://www.ncbi.nlm.nih.gov/pubmed/36874423 http://dx.doi.org/10.12998/wjcc.v11.i5.1094 |
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