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Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions

BACKGROUND: In recent years, with the development of imaging technology, the accurate diagnosis of precancerous lesions of digestive system and early lymphoma has attracted wide attention in the medical field. METHODS: In this study, 82 patients with gastrointestinal diseases, including 32 patients...

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Autores principales: Chen, Jingcong, Zhong, Yu, Zeng, Xiangling, Huang, Chunyu, Lan, Bowen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273672/
https://www.ncbi.nlm.nih.gov/pubmed/35836528
http://dx.doi.org/10.21037/tcr-22-1085
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author Chen, Jingcong
Zhong, Yu
Zeng, Xiangling
Huang, Chunyu
Lan, Bowen
author_facet Chen, Jingcong
Zhong, Yu
Zeng, Xiangling
Huang, Chunyu
Lan, Bowen
author_sort Chen, Jingcong
collection PubMed
description BACKGROUND: In recent years, with the development of imaging technology, the accurate diagnosis of precancerous lesions of digestive system and early lymphoma has attracted wide attention in the medical field. METHODS: In this study, 82 patients with gastrointestinal diseases, including 32 patients with early gastrointestinal lymphoma and 50 patients with gastrointestinal precancerous lesions, underwent dynamic contrast-enhanced computed tomography (CT) scanning. The difference (δ1, δ2) and ratio (Q1, Q2) of density between arterial phase, portal phase and plain scan were measured and compared, and the receiver operating characteristic (ROC) curve of the subjects was drawn. RESULTS: The results showed no statistically significant differences in the general condition of patients or a difference for the results of the arterial phase δ1 and Q1 between the two groups (P>0.05). However, the portal venous phase δ2 and Q2 in the early lymphoma group and in precancerous lesion group were 29.50±6.05, 41.55±10.10 Hounsfield units (HU), and 1.70±0.05, 2.06±0.31, respectively. The area under the ROC curve (AUC) values for δ2 and Q2 to identify the two diseases were 0.755 and 0.878, respectively. When δ2 and Q2 were 35.63 and 1.86 HU, the specificity was 89.60% and 67.50%, and sensitivity was 89.60% and 64.90%, respectively. When the two indexes, δ2 and Q2, were combined, the specificity and sensitivity of diagnosis were 98.99% and 56.80%, respectively. CONCLUSIONS: Dynamic contrast-enhanced CT can effectively distinguish early gastrointestinal lymphoma from precancerous lesions and improve the diagnostic accuracy.
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spelling pubmed-92736722022-07-13 Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions Chen, Jingcong Zhong, Yu Zeng, Xiangling Huang, Chunyu Lan, Bowen Transl Cancer Res Original Article BACKGROUND: In recent years, with the development of imaging technology, the accurate diagnosis of precancerous lesions of digestive system and early lymphoma has attracted wide attention in the medical field. METHODS: In this study, 82 patients with gastrointestinal diseases, including 32 patients with early gastrointestinal lymphoma and 50 patients with gastrointestinal precancerous lesions, underwent dynamic contrast-enhanced computed tomography (CT) scanning. The difference (δ1, δ2) and ratio (Q1, Q2) of density between arterial phase, portal phase and plain scan were measured and compared, and the receiver operating characteristic (ROC) curve of the subjects was drawn. RESULTS: The results showed no statistically significant differences in the general condition of patients or a difference for the results of the arterial phase δ1 and Q1 between the two groups (P>0.05). However, the portal venous phase δ2 and Q2 in the early lymphoma group and in precancerous lesion group were 29.50±6.05, 41.55±10.10 Hounsfield units (HU), and 1.70±0.05, 2.06±0.31, respectively. The area under the ROC curve (AUC) values for δ2 and Q2 to identify the two diseases were 0.755 and 0.878, respectively. When δ2 and Q2 were 35.63 and 1.86 HU, the specificity was 89.60% and 67.50%, and sensitivity was 89.60% and 64.90%, respectively. When the two indexes, δ2 and Q2, were combined, the specificity and sensitivity of diagnosis were 98.99% and 56.80%, respectively. CONCLUSIONS: Dynamic contrast-enhanced CT can effectively distinguish early gastrointestinal lymphoma from precancerous lesions and improve the diagnostic accuracy. AME Publishing Company 2022-06 /pmc/articles/PMC9273672/ /pubmed/35836528 http://dx.doi.org/10.21037/tcr-22-1085 Text en 2022 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 Original Article
Chen, Jingcong
Zhong, Yu
Zeng, Xiangling
Huang, Chunyu
Lan, Bowen
Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title_full Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title_fullStr Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title_full_unstemmed Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title_short Diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
title_sort diagnostic test of dynamic computed tomography in early gastrointestinal lymphoma and precancerous lesions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273672/
https://www.ncbi.nlm.nih.gov/pubmed/35836528
http://dx.doi.org/10.21037/tcr-22-1085
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