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Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?

The objective of this study was to assess the clinical role of apparent diffusion coefficient (ADC) analysis in noncystic focal liver lesion (FLL) classification/characterization. Six hundred liver magnetic resonances with multi-b (b = 50, 400, 800 s/mm(2)) diffusion-weighted imaging (DwI) were retr...

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Autores principales: Mungai, Francesco, Morone, Mario, Villanacci, Alberta, Bondioni, Maria Pia, Mazzoni, Lorenzo Nicola, Grazioli, Luigi, Colagrande, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602426/
https://www.ncbi.nlm.nih.gov/pubmed/25058143
http://dx.doi.org/10.1097/MD.0000000000000040
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author Mungai, Francesco
Morone, Mario
Villanacci, Alberta
Bondioni, Maria Pia
Mazzoni, Lorenzo Nicola
Grazioli, Luigi
Colagrande, Stefano
author_facet Mungai, Francesco
Morone, Mario
Villanacci, Alberta
Bondioni, Maria Pia
Mazzoni, Lorenzo Nicola
Grazioli, Luigi
Colagrande, Stefano
author_sort Mungai, Francesco
collection PubMed
description The objective of this study was to assess the clinical role of apparent diffusion coefficient (ADC) analysis in noncystic focal liver lesion (FLL) classification/characterization. Six hundred liver magnetic resonances with multi-b (b = 50, 400, 800 s/mm(2)) diffusion-weighted imaging (DwI) were retrospectively reviewed. Mean ADC was measured in 388 lesions (195 benign and 193 malignant) excluding internal necrotic areas. Cystic benign lesions were excluded from analysis. Sensitivity and specificity in distinguishing benign from malignant lesions were calculated. Analysis of variance was performed to detect differences among subgroups of solid lesions. Mean ADC of malignant lesions was 0.980 × 10(−3) mm(2)/s, significantly (P < 0.05) lower than mean ADC of benign lesions (1.433 × 10(−3) mm(2)/s). Applying an ADC cutoff of 1.066 × 10(−3) mm(2)/s, specificity and sensitivity for malignancy were respectively 86.6% and 73.6%. Of all lesions, >1/3 (39.5%) presented values lower than 1 × 10(−3) mm(2)/s, with 90.0% chance of malignancy. Above 1.5 × 10(−3) mm(2)/s (about 20% of all lesions) chance of malignancy was 9.5%. DwI cannot assist in noncystic FLL characterization, but can help in FLL classification in about half the cases.
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spelling pubmed-46024262015-10-27 Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist? Mungai, Francesco Morone, Mario Villanacci, Alberta Bondioni, Maria Pia Mazzoni, Lorenzo Nicola Grazioli, Luigi Colagrande, Stefano Medicine (Baltimore) Article The objective of this study was to assess the clinical role of apparent diffusion coefficient (ADC) analysis in noncystic focal liver lesion (FLL) classification/characterization. Six hundred liver magnetic resonances with multi-b (b = 50, 400, 800 s/mm(2)) diffusion-weighted imaging (DwI) were retrospectively reviewed. Mean ADC was measured in 388 lesions (195 benign and 193 malignant) excluding internal necrotic areas. Cystic benign lesions were excluded from analysis. Sensitivity and specificity in distinguishing benign from malignant lesions were calculated. Analysis of variance was performed to detect differences among subgroups of solid lesions. Mean ADC of malignant lesions was 0.980 × 10(−3) mm(2)/s, significantly (P < 0.05) lower than mean ADC of benign lesions (1.433 × 10(−3) mm(2)/s). Applying an ADC cutoff of 1.066 × 10(−3) mm(2)/s, specificity and sensitivity for malignancy were respectively 86.6% and 73.6%. Of all lesions, >1/3 (39.5%) presented values lower than 1 × 10(−3) mm(2)/s, with 90.0% chance of malignancy. Above 1.5 × 10(−3) mm(2)/s (about 20% of all lesions) chance of malignancy was 9.5%. DwI cannot assist in noncystic FLL characterization, but can help in FLL classification in about half the cases. Wolters Kluwer Health 2014-06-04 /pmc/articles/PMC4602426/ /pubmed/25058143 http://dx.doi.org/10.1097/MD.0000000000000040 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Article
Mungai, Francesco
Morone, Mario
Villanacci, Alberta
Bondioni, Maria Pia
Mazzoni, Lorenzo Nicola
Grazioli, Luigi
Colagrande, Stefano
Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title_full Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title_fullStr Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title_full_unstemmed Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title_short Diffusion Weighted MR and Apparent Diffusion Coefficient Measurement in Classification and Characterization of Noncystic Focal Liver Lesions: Does a Clinical Role Exist?
title_sort diffusion weighted mr and apparent diffusion coefficient measurement in classification and characterization of noncystic focal liver lesions: does a clinical role exist?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602426/
https://www.ncbi.nlm.nih.gov/pubmed/25058143
http://dx.doi.org/10.1097/MD.0000000000000040
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