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Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix
We examined the impact of chronic prostatitis on the diagnostic performance of multiparametric magnetic resonance imaging (mpMRI). In this retrospective study, 63 men underwent 3T mpMRI followed by MRI/ultrasound fusion biopsy to exclude/confirm clinically significant prostate cancer (csPCa). A tota...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066731/ https://www.ncbi.nlm.nih.gov/pubmed/33808402 http://dx.doi.org/10.3390/diagnostics11040623 |
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author | Merat, Sascha Blümlein, Theresa Klarhöfer, Markus Nickel, Dominik Singer, Gad Zöllner, Frank G. Schoenberg, Stefan O. Kubik-Huch, Rahel A. Hausmann, Daniel Hefermehl, Lukas |
author_facet | Merat, Sascha Blümlein, Theresa Klarhöfer, Markus Nickel, Dominik Singer, Gad Zöllner, Frank G. Schoenberg, Stefan O. Kubik-Huch, Rahel A. Hausmann, Daniel Hefermehl, Lukas |
author_sort | Merat, Sascha |
collection | PubMed |
description | We examined the impact of chronic prostatitis on the diagnostic performance of multiparametric magnetic resonance imaging (mpMRI). In this retrospective study, 63 men underwent 3T mpMRI followed by MRI/ultrasound fusion biopsy to exclude/confirm clinically significant prostate cancer (csPCa). A total of 93 lesions were included for evaluation. Images were assessed by two radiologists. Prostatitis was graded visually on T2-weighted and contrast-enhanced sequences. The correlation of prostatitis features with the assigned Prostate Imaging Reporting and Data System (PI-RADS) and the presence of csPCa were assessed, and the clinical and functional imaging parameters for differentiating between prostatitis and significant tumors were examined. Histopathological analysis was used as the reference standard. The rate of PI-RADS 3 scores tended to be higher in the presence of radiologically severe prostatitis compared with no/discrete prostatitis (n = 52 vs. n = 9; p = 0.225). In severe prostatitis, csPCa was determined in only 7.7% (4/52) of PI-RADS 3 lesions. In severe chronic prostatitis, a binary prostatitis suffix (e.g., PI-RADS 3 i+ versus i−) within the radiological report may help assess the limitations of mpMRI interpretability because of severe prostatitis and avoid unnecessary biopsies. Mean apparent diffusion coefficient (ADC(mean)) was the best marker (cutoff 0.93 × 10(−3) mm(2)/s) to differentiate between csPCa/non csPCa in severe prostatitis. |
format | Online Article Text |
id | pubmed-8066731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80667312021-04-25 Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix Merat, Sascha Blümlein, Theresa Klarhöfer, Markus Nickel, Dominik Singer, Gad Zöllner, Frank G. Schoenberg, Stefan O. Kubik-Huch, Rahel A. Hausmann, Daniel Hefermehl, Lukas Diagnostics (Basel) Article We examined the impact of chronic prostatitis on the diagnostic performance of multiparametric magnetic resonance imaging (mpMRI). In this retrospective study, 63 men underwent 3T mpMRI followed by MRI/ultrasound fusion biopsy to exclude/confirm clinically significant prostate cancer (csPCa). A total of 93 lesions were included for evaluation. Images were assessed by two radiologists. Prostatitis was graded visually on T2-weighted and contrast-enhanced sequences. The correlation of prostatitis features with the assigned Prostate Imaging Reporting and Data System (PI-RADS) and the presence of csPCa were assessed, and the clinical and functional imaging parameters for differentiating between prostatitis and significant tumors were examined. Histopathological analysis was used as the reference standard. The rate of PI-RADS 3 scores tended to be higher in the presence of radiologically severe prostatitis compared with no/discrete prostatitis (n = 52 vs. n = 9; p = 0.225). In severe prostatitis, csPCa was determined in only 7.7% (4/52) of PI-RADS 3 lesions. In severe chronic prostatitis, a binary prostatitis suffix (e.g., PI-RADS 3 i+ versus i−) within the radiological report may help assess the limitations of mpMRI interpretability because of severe prostatitis and avoid unnecessary biopsies. Mean apparent diffusion coefficient (ADC(mean)) was the best marker (cutoff 0.93 × 10(−3) mm(2)/s) to differentiate between csPCa/non csPCa in severe prostatitis. MDPI 2021-03-30 /pmc/articles/PMC8066731/ /pubmed/33808402 http://dx.doi.org/10.3390/diagnostics11040623 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Merat, Sascha Blümlein, Theresa Klarhöfer, Markus Nickel, Dominik Singer, Gad Zöllner, Frank G. Schoenberg, Stefan O. Kubik-Huch, Rahel A. Hausmann, Daniel Hefermehl, Lukas Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title | Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title_full | Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title_fullStr | Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title_full_unstemmed | Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title_short | Impact of Chronic Prostatitis on the PI-RADS Score 3: Proposal for the Addition of a Novel Binary Suffix |
title_sort | impact of chronic prostatitis on the pi-rads score 3: proposal for the addition of a novel binary suffix |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066731/ https://www.ncbi.nlm.nih.gov/pubmed/33808402 http://dx.doi.org/10.3390/diagnostics11040623 |
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