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Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report
BACKGROUND: Plexiform fibromyxoma (PF) is a rare mesenchymal tumor, with limited case reports worldwide. Common clinical symptoms are abdominal discomfort and bleeding signs, which frequently present slow-onset in reported cases. Herein, we report a case of gastric PF presenting as acute onset and w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895193/ https://www.ncbi.nlm.nih.gov/pubmed/35321180 http://dx.doi.org/10.12998/wjcc.v10.i7.2253 |
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author | Zhang, Rui Xia, Li-Gang Huang, Kai-Bin Chen, Nan-Di |
author_facet | Zhang, Rui Xia, Li-Gang Huang, Kai-Bin Chen, Nan-Di |
author_sort | Zhang, Rui |
collection | PubMed |
description | BACKGROUND: Plexiform fibromyxoma (PF) is a rare mesenchymal tumor, with limited case reports worldwide. Common clinical symptoms are abdominal discomfort and bleeding signs, which frequently present slow-onset in reported cases. Herein, we report a case of gastric PF presenting as acute onset and with pyemia accom-panying tumor rupture. We resected the tumor as well as the distal gastric, bulbus duodeni and gallbladder for treatment in emergency surgery. Notably, before the onset of the disease, the patient received coronavirus disease 2019 (COVID-19) vaccines. CASE SUMMARY: A 26-year-old man was admitted to our hospital, due to abdominal pain and fever after having received COVID-19 vaccines. Laboratory examination indicated severe sepsis. Computed tomography scan revealed a large mass in the abdomen. Deformation of the gastrointestinal tract was seen during gastroscopy. After failure of anti-infective treatment and symptoms of shock developed, he received an emergency surgery. We found a huge and partly ruptured mass, with thick purulence. Microscopically, the mass was composed of spindle cells with clarified cytoplasm, accompanied by myxoid stroma and arborizing blood vessels. Immunohistochemistry showed the tumor cells as positive for smooth muscle actin and succinate dehydrogenase subunit B but negative for DOG-1 and CD117. Finally, the patient was diagnosed with gastric PF and discharged from the hospital. CONCLUSION: Gastric PF manifesting as tumor rupture combined with pyemia is rare. Timely surgery is critical for optimal prognosis. |
format | Online Article Text |
id | pubmed-8895193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-88951932022-03-22 Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report Zhang, Rui Xia, Li-Gang Huang, Kai-Bin Chen, Nan-Di World J Clin Cases Case Report BACKGROUND: Plexiform fibromyxoma (PF) is a rare mesenchymal tumor, with limited case reports worldwide. Common clinical symptoms are abdominal discomfort and bleeding signs, which frequently present slow-onset in reported cases. Herein, we report a case of gastric PF presenting as acute onset and with pyemia accom-panying tumor rupture. We resected the tumor as well as the distal gastric, bulbus duodeni and gallbladder for treatment in emergency surgery. Notably, before the onset of the disease, the patient received coronavirus disease 2019 (COVID-19) vaccines. CASE SUMMARY: A 26-year-old man was admitted to our hospital, due to abdominal pain and fever after having received COVID-19 vaccines. Laboratory examination indicated severe sepsis. Computed tomography scan revealed a large mass in the abdomen. Deformation of the gastrointestinal tract was seen during gastroscopy. After failure of anti-infective treatment and symptoms of shock developed, he received an emergency surgery. We found a huge and partly ruptured mass, with thick purulence. Microscopically, the mass was composed of spindle cells with clarified cytoplasm, accompanied by myxoid stroma and arborizing blood vessels. Immunohistochemistry showed the tumor cells as positive for smooth muscle actin and succinate dehydrogenase subunit B but negative for DOG-1 and CD117. Finally, the patient was diagnosed with gastric PF and discharged from the hospital. CONCLUSION: Gastric PF manifesting as tumor rupture combined with pyemia is rare. Timely surgery is critical for optimal prognosis. Baishideng Publishing Group Inc 2022-03-06 2022-03-06 /pmc/articles/PMC8895193/ /pubmed/35321180 http://dx.doi.org/10.12998/wjcc.v10.i7.2253 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 Zhang, Rui Xia, Li-Gang Huang, Kai-Bin Chen, Nan-Di Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title | Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title_full | Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title_fullStr | Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title_full_unstemmed | Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title_short | Huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: A case report |
title_sort | huge gastric plexiform fibromyxoma presenting as pyemia by rupture of tumor: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895193/ https://www.ncbi.nlm.nih.gov/pubmed/35321180 http://dx.doi.org/10.12998/wjcc.v10.i7.2253 |
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