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Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers

The purpose of this study was to evaluate the diagnostic performance of multiparametric ultrasound (mpUS; grayscale US, color Doppler US, strain elastography, and contrast-enhanced US) in the assessment of testicular lesions with negative tumoral markers. MpUS imaging data, patient age, serum tumor...

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Autores principales: Liu, Hui, Dong, Lin, Xiang, Li-Hua, Xu, Guang, Wan, Jing, Fang, Yan, Ding, Shi-Si, Jin, Ye, Sun, Li-Ping, Xu, Hui-Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933978/
https://www.ncbi.nlm.nih.gov/pubmed/35708357
http://dx.doi.org/10.4103/aja202235
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author Liu, Hui
Dong, Lin
Xiang, Li-Hua
Xu, Guang
Wan, Jing
Fang, Yan
Ding, Shi-Si
Jin, Ye
Sun, Li-Ping
Xu, Hui-Xiong
author_facet Liu, Hui
Dong, Lin
Xiang, Li-Hua
Xu, Guang
Wan, Jing
Fang, Yan
Ding, Shi-Si
Jin, Ye
Sun, Li-Ping
Xu, Hui-Xiong
author_sort Liu, Hui
collection PubMed
description The purpose of this study was to evaluate the diagnostic performance of multiparametric ultrasound (mpUS; grayscale US, color Doppler US, strain elastography, and contrast-enhanced US) in the assessment of testicular lesions with negative tumoral markers. MpUS imaging data, patient age, serum tumor markers, scrotal pain, cryptorchidism, and related clinical information were retrospectively collected for patients who underwent mpUS examination between January 2013 and December 2019. Histologic results or follow-up examinations were used as the reference standard. In total, 83 lesions from 79 patients were included in the analysis. Fifty-six patients were finally diagnosed with benign tumors, and 23 patients were ultimately diagnosed with malignant tumors. Chi-square tests or Fisher’s exact tests were used to assess the difference between the two groups. Stepwise multivariate logistic regression analysis showed that lesion diameter (odds ratio [OR] = 1.072, P = 0.005), vascularization on color Doppler US (OR = 4.066, P = 0.001), and hyperenhancement during the early phase (OR = 6.465, P = 0.047) were significant independent risk factors for malignancy; however, when compared with neoplastic lesions, pain (OR = 0.136, P < 0.001), absence of vascularization on color Doppler US (OR = 1.680, P = 0.042), and nonenhancement during the late phase (OR = 3.461, P = 0.031) were strongly associated with nonneoplastic lesions. MpUS features are useful for differentiating testicular lesions with negative tumoral markers and improving the preoperative diagnosis, which may avoid inappropriate radical orchiectomy.
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spelling pubmed-99339782023-02-17 Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers Liu, Hui Dong, Lin Xiang, Li-Hua Xu, Guang Wan, Jing Fang, Yan Ding, Shi-Si Jin, Ye Sun, Li-Ping Xu, Hui-Xiong Asian J Androl Original Article The purpose of this study was to evaluate the diagnostic performance of multiparametric ultrasound (mpUS; grayscale US, color Doppler US, strain elastography, and contrast-enhanced US) in the assessment of testicular lesions with negative tumoral markers. MpUS imaging data, patient age, serum tumor markers, scrotal pain, cryptorchidism, and related clinical information were retrospectively collected for patients who underwent mpUS examination between January 2013 and December 2019. Histologic results or follow-up examinations were used as the reference standard. In total, 83 lesions from 79 patients were included in the analysis. Fifty-six patients were finally diagnosed with benign tumors, and 23 patients were ultimately diagnosed with malignant tumors. Chi-square tests or Fisher’s exact tests were used to assess the difference between the two groups. Stepwise multivariate logistic regression analysis showed that lesion diameter (odds ratio [OR] = 1.072, P = 0.005), vascularization on color Doppler US (OR = 4.066, P = 0.001), and hyperenhancement during the early phase (OR = 6.465, P = 0.047) were significant independent risk factors for malignancy; however, when compared with neoplastic lesions, pain (OR = 0.136, P < 0.001), absence of vascularization on color Doppler US (OR = 1.680, P = 0.042), and nonenhancement during the late phase (OR = 3.461, P = 0.031) were strongly associated with nonneoplastic lesions. MpUS features are useful for differentiating testicular lesions with negative tumoral markers and improving the preoperative diagnosis, which may avoid inappropriate radical orchiectomy. Wolters Kluwer - Medknow 2022-06-10 /pmc/articles/PMC9933978/ /pubmed/35708357 http://dx.doi.org/10.4103/aja202235 Text en Copyright: © The Author(s)(2022) https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Liu, Hui
Dong, Lin
Xiang, Li-Hua
Xu, Guang
Wan, Jing
Fang, Yan
Ding, Shi-Si
Jin, Ye
Sun, Li-Ping
Xu, Hui-Xiong
Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title_full Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title_fullStr Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title_full_unstemmed Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title_short Multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
title_sort multiparametric ultrasound for the assessment of testicular lesions with negative tumoral markers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933978/
https://www.ncbi.nlm.nih.gov/pubmed/35708357
http://dx.doi.org/10.4103/aja202235
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