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Wandering small intestinal stromal tumor: A case report
BACKGROUND: The occurrence of gastrointestinal stromal tumors (GISTs) in the small intestine is rare, and a case of wandering small intestinal stromal tumor has been rarely reported to date. Dissemination of this case can help inform future diagnosis and effective treatment. CASE SUMMARY: A 68-year-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602228/ https://www.ncbi.nlm.nih.gov/pubmed/36312500 http://dx.doi.org/10.12998/wjcc.v10.i29.10622 |
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author | Su, Jin-Zhan Fan, Shu-Feng Song, Xia Cao, Lu-Jun Su, Dong-Ying |
author_facet | Su, Jin-Zhan Fan, Shu-Feng Song, Xia Cao, Lu-Jun Su, Dong-Ying |
author_sort | Su, Jin-Zhan |
collection | PubMed |
description | BACKGROUND: The occurrence of gastrointestinal stromal tumors (GISTs) in the small intestine is rare, and a case of wandering small intestinal stromal tumor has been rarely reported to date. Dissemination of this case can help inform future diagnosis and effective treatment. CASE SUMMARY: A 68-year-old patient presented to us with tarry stools. Computed tomography showed a mobile tumor moving widely within the abdominal cavity. As the laboratory data showed a low range of red blood cells and an immediate surgery was not indicated, we performed digital subtraction angiography and embolization to achieve hemostasis. Surgical resection was performed after the patient’s condition improved. The tumor was successfully removed laparoscopically. Histological examination revealed submucosal GIST with infarction, which was of intermediate-risk, with mitotic count < 1 per 10 high-power field. Immunohistochemical studies revealed the following: CD117+, Dog1+, CD34+, SMA+, S100-, CK-, Des-, SOX-11-, STAT6-, Ki67 Hotspots 10%+. The patient was ultimately diagnosed with wandering small intestinal stromal tumor. CONCLUSION: When a highly vascularized tumor is clinically encountered in the small intestine, the possibility of stromal tumors should be considered. However, when the tumor cannot be visualized at its original location, the possibility of tumor migration is considered. |
format | Online Article Text |
id | pubmed-9602228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-96022282022-10-27 Wandering small intestinal stromal tumor: A case report Su, Jin-Zhan Fan, Shu-Feng Song, Xia Cao, Lu-Jun Su, Dong-Ying World J Clin Cases Case Report BACKGROUND: The occurrence of gastrointestinal stromal tumors (GISTs) in the small intestine is rare, and a case of wandering small intestinal stromal tumor has been rarely reported to date. Dissemination of this case can help inform future diagnosis and effective treatment. CASE SUMMARY: A 68-year-old patient presented to us with tarry stools. Computed tomography showed a mobile tumor moving widely within the abdominal cavity. As the laboratory data showed a low range of red blood cells and an immediate surgery was not indicated, we performed digital subtraction angiography and embolization to achieve hemostasis. Surgical resection was performed after the patient’s condition improved. The tumor was successfully removed laparoscopically. Histological examination revealed submucosal GIST with infarction, which was of intermediate-risk, with mitotic count < 1 per 10 high-power field. Immunohistochemical studies revealed the following: CD117+, Dog1+, CD34+, SMA+, S100-, CK-, Des-, SOX-11-, STAT6-, Ki67 Hotspots 10%+. The patient was ultimately diagnosed with wandering small intestinal stromal tumor. CONCLUSION: When a highly vascularized tumor is clinically encountered in the small intestine, the possibility of stromal tumors should be considered. However, when the tumor cannot be visualized at its original location, the possibility of tumor migration is considered. Baishideng Publishing Group Inc 2022-10-16 2022-10-16 /pmc/articles/PMC9602228/ /pubmed/36312500 http://dx.doi.org/10.12998/wjcc.v10.i29.10622 Text en ©The Author(s) 2022. 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. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Su, Jin-Zhan Fan, Shu-Feng Song, Xia Cao, Lu-Jun Su, Dong-Ying Wandering small intestinal stromal tumor: A case report |
title | Wandering small intestinal stromal tumor: A case report |
title_full | Wandering small intestinal stromal tumor: A case report |
title_fullStr | Wandering small intestinal stromal tumor: A case report |
title_full_unstemmed | Wandering small intestinal stromal tumor: A case report |
title_short | Wandering small intestinal stromal tumor: A case report |
title_sort | wandering small intestinal stromal tumor: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602228/ https://www.ncbi.nlm.nih.gov/pubmed/36312500 http://dx.doi.org/10.12998/wjcc.v10.i29.10622 |
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