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Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review
Intussusception mostly occurs in childhood and is rare in adults. Although intussusception can occur in any part of the gastrointestinal tract, gastroduodenal intussusception caused by a gastric tumor is relatively uncommon in clinical practice. A PubMed search identified 24 published cases of gastr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150259/ https://www.ncbi.nlm.nih.gov/pubmed/35632985 http://dx.doi.org/10.1177/03000605221100772 |
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author | Zhang, Wenbing Chen, Haifeng Zhu, Lulu Kong, Zhiyuan Wang, Tingting Li, Weiping |
author_facet | Zhang, Wenbing Chen, Haifeng Zhu, Lulu Kong, Zhiyuan Wang, Tingting Li, Weiping |
author_sort | Zhang, Wenbing |
collection | PubMed |
description | Intussusception mostly occurs in childhood and is rare in adults. Although intussusception can occur in any part of the gastrointestinal tract, gastroduodenal intussusception caused by a gastric tumor is relatively uncommon in clinical practice. A PubMed search identified 24 published cases of gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor (GIST); however, it is possible that we missed other cases not included in PubMed. Here we report a case of gastroduodenal intussusception caused by gastric GIST in an 85-year-old man. He came to the hospital because of recurrent black stools. Plain computed tomography (CT) scan indicated a mass in the gastric antrum, with slight enhancement in the arterial phase on enhanced CT scan. He was diagnosed with GIST. In addition, images indicated that the mass overlapped into the duodenum, and gastroduodenal intussusception was thus considered. Gastroscopy showed a huge mass in the gastric body. According to the gastroscopy and CT results, gastroduodenal intussusception caused by a gastric tumor was considered. The patient underwent complete surgical removal, which revealed a mass originating from the gastric antrum and overlapping into the duodenum. The postoperative pathological diagnosis was intermediate-risk gastric GIST. The patient was followed up for 4 months without tumor recurrence. |
format | Online Article Text |
id | pubmed-9150259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-91502592022-05-31 Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review Zhang, Wenbing Chen, Haifeng Zhu, Lulu Kong, Zhiyuan Wang, Tingting Li, Weiping J Int Med Res Case Reports Intussusception mostly occurs in childhood and is rare in adults. Although intussusception can occur in any part of the gastrointestinal tract, gastroduodenal intussusception caused by a gastric tumor is relatively uncommon in clinical practice. A PubMed search identified 24 published cases of gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor (GIST); however, it is possible that we missed other cases not included in PubMed. Here we report a case of gastroduodenal intussusception caused by gastric GIST in an 85-year-old man. He came to the hospital because of recurrent black stools. Plain computed tomography (CT) scan indicated a mass in the gastric antrum, with slight enhancement in the arterial phase on enhanced CT scan. He was diagnosed with GIST. In addition, images indicated that the mass overlapped into the duodenum, and gastroduodenal intussusception was thus considered. Gastroscopy showed a huge mass in the gastric body. According to the gastroscopy and CT results, gastroduodenal intussusception caused by a gastric tumor was considered. The patient underwent complete surgical removal, which revealed a mass originating from the gastric antrum and overlapping into the duodenum. The postoperative pathological diagnosis was intermediate-risk gastric GIST. The patient was followed up for 4 months without tumor recurrence. SAGE Publications 2022-05-27 /pmc/articles/PMC9150259/ /pubmed/35632985 http://dx.doi.org/10.1177/03000605221100772 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Zhang, Wenbing Chen, Haifeng Zhu, Lulu Kong, Zhiyuan Wang, Tingting Li, Weiping Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title | Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title_full | Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title_fullStr | Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title_full_unstemmed | Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title_short | Gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
title_sort | gastroduodenal intussusception caused by gastric gastrointestinal stromal tumor in adults: a case report and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150259/ https://www.ncbi.nlm.nih.gov/pubmed/35632985 http://dx.doi.org/10.1177/03000605221100772 |
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