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The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma

BACKGROUND: To define a threshold value of apparent diffusion coefficient (ADC) with which malignant breast lesions can be distinguished from benign lesions, and to evaluate the ADC change of peri-tumor tissue in breast carcinoma by echo planar-diffusion weighted imaging (EPI-DWI). METHODS: 57 breas...

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Autores principales: Yili, Zhang, Xiaoyan, Huang, Hongwen, Du, Yun, Zhang, Xin, Chen, Peng, Wang, Youmin, Guo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633008/
https://www.ncbi.nlm.nih.gov/pubmed/19144163
http://dx.doi.org/10.1186/1471-2407-9-18
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author Yili, Zhang
Xiaoyan, Huang
Hongwen, Du
Yun, Zhang
Xin, Chen
Peng, Wang
Youmin, Guo
author_facet Yili, Zhang
Xiaoyan, Huang
Hongwen, Du
Yun, Zhang
Xin, Chen
Peng, Wang
Youmin, Guo
author_sort Yili, Zhang
collection PubMed
description BACKGROUND: To define a threshold value of apparent diffusion coefficient (ADC) with which malignant breast lesions can be distinguished from benign lesions, and to evaluate the ADC change of peri-tumor tissue in breast carcinoma by echo planar-diffusion weighted imaging (EPI-DWI). METHODS: 57 breast lesions were scanned by routine MRI and EPI-DWI. The ADC values were compared between malignant and benign lesions. The sensitivity and specificity of EPI-DWI and the threshold ADC value were evaluated by Receiver Operating Characteristic curve (ROC). The ADC values of malignant lesion and layered peri-tumor tissues (from innermost layer 1 to outermost layer 4 with 5 mm every layer) in different directions were compared and the ADC values among different layers were compared. RESULTS: The ADC value of 35 malignant lesions was statistically lower than that of 22 benign lesions (P < 0.05). In ROC curve, the threshold value was 1.24 +/- 0.25*10E-3 mm(2)/s (b = 500) or 1.20 +/- 0.25*10E-3 mm(2)/s (b = 1000). The ADC value of malignant lesions was statistically lower than that of peri-tumor tissues in different directions (P < 0.05). For peri-tumor tissues, the ADC values increased gradually from layer 1 to layer 4 and there was a significant difference between the ADC values of layer 1 and layer 2 (P < 0.05); while from layer 2 outwards, there was no statistical difference among different layers. CONCLUSION: ADC value was a sensitive and specific parameter that could help to differentiate benign and malignant breast lesions. ADC changes in tissues adjacent to breast carcinoma could be detected by EPI-DWI, which made EPI-DWI a promising method for helping to determine surgical scope of breast carcinoma.
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spelling pubmed-26330082009-01-30 The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma Yili, Zhang Xiaoyan, Huang Hongwen, Du Yun, Zhang Xin, Chen Peng, Wang Youmin, Guo BMC Cancer Research Article BACKGROUND: To define a threshold value of apparent diffusion coefficient (ADC) with which malignant breast lesions can be distinguished from benign lesions, and to evaluate the ADC change of peri-tumor tissue in breast carcinoma by echo planar-diffusion weighted imaging (EPI-DWI). METHODS: 57 breast lesions were scanned by routine MRI and EPI-DWI. The ADC values were compared between malignant and benign lesions. The sensitivity and specificity of EPI-DWI and the threshold ADC value were evaluated by Receiver Operating Characteristic curve (ROC). The ADC values of malignant lesion and layered peri-tumor tissues (from innermost layer 1 to outermost layer 4 with 5 mm every layer) in different directions were compared and the ADC values among different layers were compared. RESULTS: The ADC value of 35 malignant lesions was statistically lower than that of 22 benign lesions (P < 0.05). In ROC curve, the threshold value was 1.24 +/- 0.25*10E-3 mm(2)/s (b = 500) or 1.20 +/- 0.25*10E-3 mm(2)/s (b = 1000). The ADC value of malignant lesions was statistically lower than that of peri-tumor tissues in different directions (P < 0.05). For peri-tumor tissues, the ADC values increased gradually from layer 1 to layer 4 and there was a significant difference between the ADC values of layer 1 and layer 2 (P < 0.05); while from layer 2 outwards, there was no statistical difference among different layers. CONCLUSION: ADC value was a sensitive and specific parameter that could help to differentiate benign and malignant breast lesions. ADC changes in tissues adjacent to breast carcinoma could be detected by EPI-DWI, which made EPI-DWI a promising method for helping to determine surgical scope of breast carcinoma. BioMed Central 2009-01-14 /pmc/articles/PMC2633008/ /pubmed/19144163 http://dx.doi.org/10.1186/1471-2407-9-18 Text en Copyright ©2009 Yili et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yili, Zhang
Xiaoyan, Huang
Hongwen, Du
Yun, Zhang
Xin, Chen
Peng, Wang
Youmin, Guo
The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title_full The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title_fullStr The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title_full_unstemmed The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title_short The value of diffusion-weighted imaging in assessing the ADC changes of tissues adjacent to breast carcinoma
title_sort value of diffusion-weighted imaging in assessing the adc changes of tissues adjacent to breast carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633008/
https://www.ncbi.nlm.nih.gov/pubmed/19144163
http://dx.doi.org/10.1186/1471-2407-9-18
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