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Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging

PURPOSE: To retrospectively evaluate the effect of post-prostate-biopsy hemorrhage on the interpretation of magnetic resonance diffusion-weighted (MRDW) and magnetic resonance spectroscopic (MRS) imaging in the detection of prostate cancer. We also investigated the optimal timing for magnetic resona...

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Autores principales: Lee, Jong Yeon, Chang, In Ho, Moon, Young Tae, Kim, Kyung Do, Myung, Soon Chul, Kim, Tae Hyoung, Lee, Jong Beum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Urological Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212661/
https://www.ncbi.nlm.nih.gov/pubmed/22087361
http://dx.doi.org/10.4111/kju.2011.52.10.674
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author Lee, Jong Yeon
Chang, In Ho
Moon, Young Tae
Kim, Kyung Do
Myung, Soon Chul
Kim, Tae Hyoung
Lee, Jong Beum
author_facet Lee, Jong Yeon
Chang, In Ho
Moon, Young Tae
Kim, Kyung Do
Myung, Soon Chul
Kim, Tae Hyoung
Lee, Jong Beum
author_sort Lee, Jong Yeon
collection PubMed
description PURPOSE: To retrospectively evaluate the effect of post-prostate-biopsy hemorrhage on the interpretation of magnetic resonance diffusion-weighted (MRDW) and magnetic resonance spectroscopic (MRS) imaging in the detection of prostate cancer. We also investigated the optimal timing for magnetic resonance examination after prostate biopsy. MATERIALS AND METHODS: We reviewed the records of 135 men. All patients underwent prostate magnetic resonance imaging (MRI). The prostate was divided into eight regions according to the biopsy site. Subsequently, we measured hemorrhage on apparent diffusion coefficient (ADC) values and (choline+creatinine)/citrate ([Cho+Cr]/Cit) ratios in the same regions on the MRI. We investigated the effect of hemorrhage at ADC values and (Cho+Cr)/Cit ratios on MRI and the relationship between prostate biopsy results and MRI findings. RESULTS: The mean patient age was 68.7 years and the mean time between biopsy and MRI was 23.5 days. The total hemorrhagic score demonstrated no significant associations with intervals from biopsy to MRI. Higher hemorrhagic scores were associated with higher ADC values, prostate cancer, and noncancer groups, respectively (p<0.001). ADC values were lower in tumors than in normal tissue (p<0.001), and ADC values were inversely correlated with tumor Gleason score in biopsy cores (p<0.001). However, (Cho+Cr)/Cit ratios did not exhibit any association with prostate biopsy results and hemorrhage. CONCLUSIONS: Hemorrhage had no significant associations with the interval from biopsy to MRI. ADC values may help to detect prostate cancer and predict the aggressiveness of cancer; however, it is important to consider the bias effect of hemorrhage on the interpretation of MRDW imaging given that hemorrhage affects ADC values.
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spelling pubmed-32126612011-11-15 Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging Lee, Jong Yeon Chang, In Ho Moon, Young Tae Kim, Kyung Do Myung, Soon Chul Kim, Tae Hyoung Lee, Jong Beum Korean J Urol Original Article PURPOSE: To retrospectively evaluate the effect of post-prostate-biopsy hemorrhage on the interpretation of magnetic resonance diffusion-weighted (MRDW) and magnetic resonance spectroscopic (MRS) imaging in the detection of prostate cancer. We also investigated the optimal timing for magnetic resonance examination after prostate biopsy. MATERIALS AND METHODS: We reviewed the records of 135 men. All patients underwent prostate magnetic resonance imaging (MRI). The prostate was divided into eight regions according to the biopsy site. Subsequently, we measured hemorrhage on apparent diffusion coefficient (ADC) values and (choline+creatinine)/citrate ([Cho+Cr]/Cit) ratios in the same regions on the MRI. We investigated the effect of hemorrhage at ADC values and (Cho+Cr)/Cit ratios on MRI and the relationship between prostate biopsy results and MRI findings. RESULTS: The mean patient age was 68.7 years and the mean time between biopsy and MRI was 23.5 days. The total hemorrhagic score demonstrated no significant associations with intervals from biopsy to MRI. Higher hemorrhagic scores were associated with higher ADC values, prostate cancer, and noncancer groups, respectively (p<0.001). ADC values were lower in tumors than in normal tissue (p<0.001), and ADC values were inversely correlated with tumor Gleason score in biopsy cores (p<0.001). However, (Cho+Cr)/Cit ratios did not exhibit any association with prostate biopsy results and hemorrhage. CONCLUSIONS: Hemorrhage had no significant associations with the interval from biopsy to MRI. ADC values may help to detect prostate cancer and predict the aggressiveness of cancer; however, it is important to consider the bias effect of hemorrhage on the interpretation of MRDW imaging given that hemorrhage affects ADC values. The Korean Urological Association 2011-10 2011-10-19 /pmc/articles/PMC3212661/ /pubmed/22087361 http://dx.doi.org/10.4111/kju.2011.52.10.674 Text en © The Korean Urological Association, 2011 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Jong Yeon
Chang, In Ho
Moon, Young Tae
Kim, Kyung Do
Myung, Soon Chul
Kim, Tae Hyoung
Lee, Jong Beum
Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title_full Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title_fullStr Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title_full_unstemmed Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title_short Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging
title_sort effect of prostate biopsy hemorrhage on mrdw and mrs imaging
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212661/
https://www.ncbi.nlm.nih.gov/pubmed/22087361
http://dx.doi.org/10.4111/kju.2011.52.10.674
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