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Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma

Clinical value of magnetic resonance imaging (MRI) in identifying and diagnosing multiple cerebral glioma (MCG) from primary central nervous system lymphoma (PCNSL) was evaluated. A total of 21 patients with MCG diagnosed clinically and pathologically in Zhangzhou Municipal Hospital from March 2016...

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Autores principales: Chen, Yushan, Zhan, Alai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540358/
https://www.ncbi.nlm.nih.gov/pubmed/31289531
http://dx.doi.org/10.3892/ol.2019.10352
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author Chen, Yushan
Zhan, Alai
author_facet Chen, Yushan
Zhan, Alai
author_sort Chen, Yushan
collection PubMed
description Clinical value of magnetic resonance imaging (MRI) in identifying and diagnosing multiple cerebral glioma (MCG) from primary central nervous system lymphoma (PCNSL) was evaluated. A total of 21 patients with MCG diagnosed clinically and pathologically in Zhangzhou Municipal Hospital from March 2016 to April 2017 were selected as group A, and 30 patients with PCNSL diagnosed in Zhangzhou Affiliated Hospital of Fujian Medical University during the same period as group B. Plain MRI, enhanced MRI and diffusion weighted imaging (DWI) were performed in all patients, the apparent diffusion coefficient (ADC) value of lesions was measured, and the diagnostic efficacy of ADC for MCG and PCNSL was evaluated by receiver operating characteristic (ROC) curve. The incidence of hippocampus lesions, patchy and cystic lesions, and the heterogeneous signal of plain scan in group A was significantly higher than that in group B (P<0.05), and the incidence of basal ganglia lesions was significantly lower than that in group B (P<0.05). Mass lesions in group A were significantly less than those in group B (P<0.05). The ADC value of lesions in group A was significantly higher than that in contralateral normal white matter (P<0.05), the ADC value in group B was significantly lower than that in normal contralateral white matter (P<0.05), so the ADC value in group A was significantly higher than that in group B (P<0.05). The location, lesion shape and signal characteristic of MCG and PCNSL have their own specificity; there are significant differences in DWI signal and ADC color map signal intensity of the lesions; ADC has certain diagnostic value for MCG and PCNSL; the differential diagnosis of MCG from PCNSL by MRI is of great significance.
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spelling pubmed-65403582019-07-09 Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma Chen, Yushan Zhan, Alai Oncol Lett Articles Clinical value of magnetic resonance imaging (MRI) in identifying and diagnosing multiple cerebral glioma (MCG) from primary central nervous system lymphoma (PCNSL) was evaluated. A total of 21 patients with MCG diagnosed clinically and pathologically in Zhangzhou Municipal Hospital from March 2016 to April 2017 were selected as group A, and 30 patients with PCNSL diagnosed in Zhangzhou Affiliated Hospital of Fujian Medical University during the same period as group B. Plain MRI, enhanced MRI and diffusion weighted imaging (DWI) were performed in all patients, the apparent diffusion coefficient (ADC) value of lesions was measured, and the diagnostic efficacy of ADC for MCG and PCNSL was evaluated by receiver operating characteristic (ROC) curve. The incidence of hippocampus lesions, patchy and cystic lesions, and the heterogeneous signal of plain scan in group A was significantly higher than that in group B (P<0.05), and the incidence of basal ganglia lesions was significantly lower than that in group B (P<0.05). Mass lesions in group A were significantly less than those in group B (P<0.05). The ADC value of lesions in group A was significantly higher than that in contralateral normal white matter (P<0.05), the ADC value in group B was significantly lower than that in normal contralateral white matter (P<0.05), so the ADC value in group A was significantly higher than that in group B (P<0.05). The location, lesion shape and signal characteristic of MCG and PCNSL have their own specificity; there are significant differences in DWI signal and ADC color map signal intensity of the lesions; ADC has certain diagnostic value for MCG and PCNSL; the differential diagnosis of MCG from PCNSL by MRI is of great significance. D.A. Spandidos 2019-07 2019-05-13 /pmc/articles/PMC6540358/ /pubmed/31289531 http://dx.doi.org/10.3892/ol.2019.10352 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Chen, Yushan
Zhan, Alai
Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title_full Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title_fullStr Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title_full_unstemmed Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title_short Clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
title_sort clinical value of magnetic resonance imaging in identifying multiple cerebral gliomas from primary central nervous system lymphoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540358/
https://www.ncbi.nlm.nih.gov/pubmed/31289531
http://dx.doi.org/10.3892/ol.2019.10352
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