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Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature
Primary synovial sarcoma of the duodenal bulb is a rare mesenchymal tumor with special morphological features. It usually originates from the major joints or tendon sheaths of the extremities and mostly seen in young population, but rarely found in gastrointestinal tract. In this manuscript, we repo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799197/ https://www.ncbi.nlm.nih.gov/pubmed/35117930 http://dx.doi.org/10.21037/tcr-20-1107 |
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author | Yang, Hanteng Cheng, Xiaocheng Zhu, Wei Xiao, Jingying Li, Fan Ren, Yanxian Wang, Keshen Jiao, Zuoyi Luo, Changjiang |
author_facet | Yang, Hanteng Cheng, Xiaocheng Zhu, Wei Xiao, Jingying Li, Fan Ren, Yanxian Wang, Keshen Jiao, Zuoyi Luo, Changjiang |
author_sort | Yang, Hanteng |
collection | PubMed |
description | Primary synovial sarcoma of the duodenal bulb is a rare mesenchymal tumor with special morphological features. It usually originates from the major joints or tendon sheaths of the extremities and mostly seen in young population, but rarely found in gastrointestinal tract. In this manuscript, we reported the first case of synovial sarcoma arising between the intestinal wall of the duodenal bulb with a concomitant SYT/SSX type of the t(X;18) translocation. A 49-year-old male presented to our hospital with a 2-month history of upper abdominal pain along with a 4-day amply jaundice. Tumor marker testing showed only a slight increase of carbohydrate antigen 19-9 (CA19-9). A computed tomography scan of his abdomen showed that indeterminate tissue occupied the duodenal bulb wall, compressed the surrounding tissues, and measured roughly 5.0 cm × 7.7 cm × 8.7 cm. Since the sarcoma grows between the intestinal wall, which cannot be detected by endoscopy, an initial diagnosis of duodenal wall stromal tumor was made at that time. Postoperative Immunohistochemistry results showed that the tumor was positive for the expression of transducin-like enhancer of split 1, B-cell lymphoma 2, and Vimentin. These pathological findings were indicative of the diagnosis of synovial sarcoma, but still did not provide sufficient diagnostic evidence. Finally we confirmed the diagnosis by using fluorescence in situ hybridization (FISH) with detection of the t(X;18) (SYT-SSX) translocation. No such lesions were found on preoperative examination, so a diagnosis of primary duodenal synovial sarcoma was made. After literature review, we found four reports of duodenal synovial sarcomas, all of which could be detected endoscopically, but there were no results of long-term follow-up. This case is the first reported case of synovial sarcoma arising between the intestinal walls of the duodenal bulb treated twice with ifosfamide and followed up for 13 months without recurrence. |
format | Online Article Text |
id | pubmed-8799197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87991972022-02-02 Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature Yang, Hanteng Cheng, Xiaocheng Zhu, Wei Xiao, Jingying Li, Fan Ren, Yanxian Wang, Keshen Jiao, Zuoyi Luo, Changjiang Transl Cancer Res Case Report Primary synovial sarcoma of the duodenal bulb is a rare mesenchymal tumor with special morphological features. It usually originates from the major joints or tendon sheaths of the extremities and mostly seen in young population, but rarely found in gastrointestinal tract. In this manuscript, we reported the first case of synovial sarcoma arising between the intestinal wall of the duodenal bulb with a concomitant SYT/SSX type of the t(X;18) translocation. A 49-year-old male presented to our hospital with a 2-month history of upper abdominal pain along with a 4-day amply jaundice. Tumor marker testing showed only a slight increase of carbohydrate antigen 19-9 (CA19-9). A computed tomography scan of his abdomen showed that indeterminate tissue occupied the duodenal bulb wall, compressed the surrounding tissues, and measured roughly 5.0 cm × 7.7 cm × 8.7 cm. Since the sarcoma grows between the intestinal wall, which cannot be detected by endoscopy, an initial diagnosis of duodenal wall stromal tumor was made at that time. Postoperative Immunohistochemistry results showed that the tumor was positive for the expression of transducin-like enhancer of split 1, B-cell lymphoma 2, and Vimentin. These pathological findings were indicative of the diagnosis of synovial sarcoma, but still did not provide sufficient diagnostic evidence. Finally we confirmed the diagnosis by using fluorescence in situ hybridization (FISH) with detection of the t(X;18) (SYT-SSX) translocation. No such lesions were found on preoperative examination, so a diagnosis of primary duodenal synovial sarcoma was made. After literature review, we found four reports of duodenal synovial sarcomas, all of which could be detected endoscopically, but there were no results of long-term follow-up. This case is the first reported case of synovial sarcoma arising between the intestinal walls of the duodenal bulb treated twice with ifosfamide and followed up for 13 months without recurrence. AME Publishing Company 2020-09 /pmc/articles/PMC8799197/ /pubmed/35117930 http://dx.doi.org/10.21037/tcr-20-1107 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Case Report Yang, Hanteng Cheng, Xiaocheng Zhu, Wei Xiao, Jingying Li, Fan Ren, Yanxian Wang, Keshen Jiao, Zuoyi Luo, Changjiang Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title | Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title_full | Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title_fullStr | Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title_full_unstemmed | Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title_short | Primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
title_sort | primary synovial sarcoma of the duodenal bulb: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799197/ https://www.ncbi.nlm.nih.gov/pubmed/35117930 http://dx.doi.org/10.21037/tcr-20-1107 |
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