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Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors
OBJECTIVES: To explore the clinical significance of (18)F-FDG metabolic imaging in the diagnosis and biological risk assessment of gastrointestinal stromal tumors (GIST). METHODS: This study is a clinical retrospective study. The research subjects were patients with GIST who were admitted to our hos...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479238/ https://www.ncbi.nlm.nih.gov/pubmed/36114563 http://dx.doi.org/10.1186/s40001-022-00806-9 |
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author | Du, Wen Cui, Guojin Wang, Kaiping Li, Shaojie |
author_facet | Du, Wen Cui, Guojin Wang, Kaiping Li, Shaojie |
author_sort | Du, Wen |
collection | PubMed |
description | OBJECTIVES: To explore the clinical significance of (18)F-FDG metabolic imaging in the diagnosis and biological risk assessment of gastrointestinal stromal tumors (GIST). METHODS: This study is a clinical retrospective study. The research subjects were patients with GIST who were admitted to our hospital from January 2014 to December 2019 and underwent (18)F-FDG metabolic imaging, and the relationship between biological risk and FDG metabolism was analyzed retrospectively. RESULTS: A total of 32 patients with GIST were included in this study, of which 17 patients had very low and low-risk lesions, and the FDG metabolism level did not increase; five patients had moderate-risk gastric lesions, and the FDG metabolism level was abnormally increased; 10 patients had high-risk lesions, and except for one patient with multiple lesions, the FDG metabolism level of these patients was increased. CONCLUSIONS: The level of glucose metabolism is abnormally increased in tumor cells with vigorous mitosis and has higher biological risk. The (18)F-FDG metabolism level can determine the biological risk of GIST and whether high-risk lesions involve other tissues and organs, as it more comprehensively reflects the distribution of lesions, the activity of tumor cells and the stage of the disease. |
format | Online Article Text |
id | pubmed-9479238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94792382022-09-17 Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors Du, Wen Cui, Guojin Wang, Kaiping Li, Shaojie Eur J Med Res Research OBJECTIVES: To explore the clinical significance of (18)F-FDG metabolic imaging in the diagnosis and biological risk assessment of gastrointestinal stromal tumors (GIST). METHODS: This study is a clinical retrospective study. The research subjects were patients with GIST who were admitted to our hospital from January 2014 to December 2019 and underwent (18)F-FDG metabolic imaging, and the relationship between biological risk and FDG metabolism was analyzed retrospectively. RESULTS: A total of 32 patients with GIST were included in this study, of which 17 patients had very low and low-risk lesions, and the FDG metabolism level did not increase; five patients had moderate-risk gastric lesions, and the FDG metabolism level was abnormally increased; 10 patients had high-risk lesions, and except for one patient with multiple lesions, the FDG metabolism level of these patients was increased. CONCLUSIONS: The level of glucose metabolism is abnormally increased in tumor cells with vigorous mitosis and has higher biological risk. The (18)F-FDG metabolism level can determine the biological risk of GIST and whether high-risk lesions involve other tissues and organs, as it more comprehensively reflects the distribution of lesions, the activity of tumor cells and the stage of the disease. BioMed Central 2022-09-16 /pmc/articles/PMC9479238/ /pubmed/36114563 http://dx.doi.org/10.1186/s40001-022-00806-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Du, Wen Cui, Guojin Wang, Kaiping Li, Shaojie Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title | Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title_full | Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title_fullStr | Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title_full_unstemmed | Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title_short | Clinical significance of (18)F-FDG PET/CT imaging in 32 cases of gastrointestinal stromal tumors |
title_sort | clinical significance of (18)f-fdg pet/ct imaging in 32 cases of gastrointestinal stromal tumors |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479238/ https://www.ncbi.nlm.nih.gov/pubmed/36114563 http://dx.doi.org/10.1186/s40001-022-00806-9 |
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