Mario Henrique Bitar Siqueira, Deborah Jakubowicz, Roseanne Ferreira, Sagi Shprits, Omar Buksh, Naeem Bhojani, Bilal Chughtai, Kevin C Zorn, Luca Cindolo, Giovanni Ferrari, Lorenzo Gatti, Katherine Lajkosz, Dean Elterman
Introduction: Water vapor thermal therapy (WVTT), Rezūm, is a minimally invasive therapy that uses water vapor to ablate benign prostatic tissue. This study aimed to present the prospective, multicenter outcomes of the largest cohort of prostates ≥80 mL treated with Rezūm.
Methods: This study involved a prospective, WVTT registry that collated information from two high-volume centers between April 2019 and August 2024. Baseline medical histories, uroflowmetry (peak flow rate [Qmax], postvoid residual [PVR], and validated questionnaires (International Prostate Symptom Score [IPSS], IPSS quality of life (QoL), Benign Prostatic Hyperplasia Impact Index [BPHII], International Index of Erectile Function [IIEF-15], Male Sexual Health Questionnaire for Ejaculatory Dysfunction [MSHQ-EjD]) were recorded. The main outcomes assessed included symptom scores, functional improvement, and safety at baseline, six, 12, and 24 months.
Results: A total of 259 patients with a prostate volume ≥80 mL were treated with Rezūm. The median prostate volume was 105 mL, with 207 patients (81.2%) exhibiting a median lobe. The IPSS improved from 21.8 at baseline to 5.7 at 24 months. The IPSS QoL score improved from 4.5 at baseline to 1.1 at 24 months. At baseline, the Qmax rate was 8.2 mL/s, increasing to 14.9 mL/s at 24 months. PVR volume decreased from 132.5 mL at baseline to 90 mL at 24 months. The BPHII decreased from 7.5 at baseline to 2.3 at 24 months. There was no significant change in sexual function as measured by IIEF and MSHQ.
Conclusions: Rezūm therapy is a safe, effective, and minimally invasive option for managing large prostates (≥80 mL), providing significant and sustained improvements in urinary symptoms with minimal impact on sexual function.
{"title":"Rezūm water vapor thermal therapy for large-volume (≥80 mL), symptomatic, benign prostatic enlargement: Large, multicenter, real-world cohort with two-year followup.","authors":"Mario Henrique Bitar Siqueira, Deborah Jakubowicz, Roseanne Ferreira, Sagi Shprits, Omar Buksh, Naeem Bhojani, Bilal Chughtai, Kevin C Zorn, Luca Cindolo, Giovanni Ferrari, Lorenzo Gatti, Katherine Lajkosz, Dean Elterman","doi":"10.5489/cuaj.9336","DOIUrl":"https://doi.org/10.5489/cuaj.9336","url":null,"abstract":"<p><strong>Introduction: </strong>Water vapor thermal therapy (WVTT), Rezūm, is a minimally invasive therapy that uses water vapor to ablate benign prostatic tissue. This study aimed to present the prospective, multicenter outcomes of the largest cohort of prostates ≥80 mL treated with Rezūm.</p><p><strong>Methods: </strong>This study involved a prospective, WVTT registry that collated information from two high-volume centers between April 2019 and August 2024. Baseline medical histories, uroflowmetry (peak flow rate [Qmax], postvoid residual [PVR], and validated questionnaires (International Prostate Symptom Score [IPSS], IPSS quality of life (QoL), Benign Prostatic Hyperplasia Impact Index [BPHII], International Index of Erectile Function [IIEF-15], Male Sexual Health Questionnaire for Ejaculatory Dysfunction [MSHQ-EjD]) were recorded. The main outcomes assessed included symptom scores, functional improvement, and safety at baseline, six, 12, and 24 months.</p><p><strong>Results: </strong>A total of 259 patients with a prostate volume ≥80 mL were treated with Rezūm. The median prostate volume was 105 mL, with 207 patients (81.2%) exhibiting a median lobe. The IPSS improved from 21.8 at baseline to 5.7 at 24 months. The IPSS QoL score improved from 4.5 at baseline to 1.1 at 24 months. At baseline, the Qmax rate was 8.2 mL/s, increasing to 14.9 mL/s at 24 months. PVR volume decreased from 132.5 mL at baseline to 90 mL at 24 months. The BPHII decreased from 7.5 at baseline to 2.3 at 24 months. There was no significant change in sexual function as measured by IIEF and MSHQ.</p><p><strong>Conclusions: </strong>Rezūm therapy is a safe, effective, and minimally invasive option for managing large prostates (≥80 mL), providing significant and sustained improvements in urinary symptoms with minimal impact on sexual function.</p>","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Case - Non-metastatic castration-resistant prostate cancer in a transgender woman.","authors":"Matthew Mancuso, Howard Evans, Lucas Dean","doi":"10.5489/cuaj.9278","DOIUrl":"https://doi.org/10.5489/cuaj.9278","url":null,"abstract":"","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ziv Savin, Reuben Ben-David, Avishay Shem-Tov Dlugy, Natasha Oppenheim, Ron Marom, Yotam Veredgorn, Haim Herzberg, Snir Dekalo, Gal Keren-Paz, Roy Mano, Ofer Yossepowitch
Introduction: Active surveillance (AS) requires regular monitoring to detect disease progression. Multiparametric magnetic resonance imaging (mpMRI) and targeted biopsies are commonly used to identify clinically significant prostate cancer (csPC) in AS patients, yet their diagnostic value remains unclear among this population.
Methods: We conducted a retrospective study of patients who underwent mpMRI followed by combined prostate biopsies between 2017 and 2022. Patients were categorized into AS and non-AS groups. We compared the diagnostic yield of mpMRI suspicious Prostate Imaging-Reporting & Data System (PI-RADS) 3-5 lesions using comparisons of PI-RADS score distribution and detection rates of csPC from targeted biopsies between the groups. Logistic regression was used to assess associations between AS category and outcomes. csPC detection rates of targeted and combined biopsies were assessed as well.
Results: The study consisted of 600 patients, 158 in the AS group and 442 in the non-AS group. PI-RADS scores distribution and the number of suspicious lesions were similar between AS and non-AS groups. csPC detection rates from targeted biopsies were not different between AS and non-AS patients (32% vs. 30%, p=0.68), and AS was also not associated with the rates of csPC for each PI-RADS score. The addition of systematic biopsies did not increase csPC detection in AS patients (36% vs. 32%, p=0.47).
Conclusions: Our findings suggest that mpMRI suspicious PI-RADS 3-5 lesions are reliable for csPC diagnosis during AS, and that targeted biopsies alone may be sufficient for its detection; however, further prospective research is needed to validate these results and optimize biopsy strategies within AS protocols.
主动监测(AS)需要定期监测以发现疾病进展。多参数磁共振成像(mpMRI)和靶向活检通常用于识别AS患者的临床显著前列腺癌(csPC),但其在该人群中的诊断价值尚不清楚。方法:我们对2017年至2022年间接受mpMRI和联合前列腺活检的患者进行了回顾性研究。患者分为AS组和非AS组。我们比较了mpMRI可疑前列腺影像报告和数据系统(PI-RADS) 3-5病变的诊出率,比较了两组间PI-RADS评分分布和靶向活检csPC的检出率。使用逻辑回归来评估AS类别与结果之间的关联。同时评估靶向活检和联合活检的csPC检出率。结果:研究共纳入600例患者,其中AS组158例,非AS组442例。AS组与非AS组PI-RADS评分分布及可疑病灶数量相似。靶向活检的csPC检出率在AS和非AS患者之间没有差异(32% vs 30%, p=0.68),并且AS也与每次PI-RADS评分的csPC检出率无关。增加系统活检并没有增加AS患者的csPC检测(36% vs. 32%, p=0.47)。结论:我们的研究结果表明,mpMRI可疑PI-RADS 3-5病变对AS期间的csPC诊断是可靠的,单独的靶向活检可能足以检测到它;然而,需要进一步的前瞻性研究来验证这些结果并优化AS方案中的活检策略。
{"title":"MRI suspicious lesions in patients under active surveillance: Do systematic biopsies still add value?","authors":"Ziv Savin, Reuben Ben-David, Avishay Shem-Tov Dlugy, Natasha Oppenheim, Ron Marom, Yotam Veredgorn, Haim Herzberg, Snir Dekalo, Gal Keren-Paz, Roy Mano, Ofer Yossepowitch","doi":"10.5489/cuaj.9254","DOIUrl":"https://doi.org/10.5489/cuaj.9254","url":null,"abstract":"<p><strong>Introduction: </strong>Active surveillance (AS) requires regular monitoring to detect disease progression. Multiparametric magnetic resonance imaging (mpMRI) and targeted biopsies are commonly used to identify clinically significant prostate cancer (csPC) in AS patients, yet their diagnostic value remains unclear among this population.</p><p><strong>Methods: </strong>We conducted a retrospective study of patients who underwent mpMRI followed by combined prostate biopsies between 2017 and 2022. Patients were categorized into AS and non-AS groups. We compared the diagnostic yield of mpMRI suspicious Prostate Imaging-Reporting & Data System (PI-RADS) 3-5 lesions using comparisons of PI-RADS score distribution and detection rates of csPC from targeted biopsies between the groups. Logistic regression was used to assess associations between AS category and outcomes. csPC detection rates of targeted and combined biopsies were assessed as well.</p><p><strong>Results: </strong>The study consisted of 600 patients, 158 in the AS group and 442 in the non-AS group. PI-RADS scores distribution and the number of suspicious lesions were similar between AS and non-AS groups. csPC detection rates from targeted biopsies were not different between AS and non-AS patients (32% vs. 30%, p=0.68), and AS was also not associated with the rates of csPC for each PI-RADS score. The addition of systematic biopsies did not increase csPC detection in AS patients (36% vs. 32%, p=0.47).</p><p><strong>Conclusions: </strong>Our findings suggest that mpMRI suspicious PI-RADS 3-5 lesions are reliable for csPC diagnosis during AS, and that targeted biopsies alone may be sufficient for its detection; however, further prospective research is needed to validate these results and optimize biopsy strategies within AS protocols.</p>","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: This study aimed to evaluate the performance of three artificial intelligence (AI) models - ChatGPT, Gemini, and Copilot - in addressing priapism-related inquiries. The accuracy, comprehensiveness, and clinical applicability of AI-generated responses were systematically analyzed.
Methods: Frequently asked questions (FAQs) regarding priapism were collected from medical guidelines, literature, and online health platforms. Each AI model generated responses, which were independently assessed by two experts based on accuracy, fluency, and clinical relevance. The Global Quality Score (GQS) was used for evaluation. Statistical analysis was performed using one-way ANOVA, with a significance threshold of p<0.05.
Results: ChatGPT and Gemini demonstrated comparable performance across all thematic categories, with mean scores ranging from 4.5-4.9, while Copilot showed significantly lower scores (3.2-4.2, p<0.001). Both ChatGPT and Gemini provided clinically relevant and accurate information, whereas Copilot's responses frequently lacked guideline-based recommendations.
Conclusions: ChatGPT and Gemini were statistically comparable in generating reliable, clinically useful responses, making them valuable tools for medical education and patient counseling. Copilot, however, exhibited lower accuracy and applicability. These findings highlight the need for continuous refinement of AI models to enhance their role in clinical decision-making while ensuring human expertise remains central to patient care.
{"title":"Comparative assessment of AI models in addressing questions on priapism: An evaluation of response quality and clinical utility.","authors":"Halis Ahmet, Hacibey Ibrahim","doi":"10.5489/cuaj.9302","DOIUrl":"https://doi.org/10.5489/cuaj.9302","url":null,"abstract":"<p><strong>Introduction: </strong>This study aimed to evaluate the performance of three artificial intelligence (AI) models - ChatGPT, Gemini, and Copilot - in addressing priapism-related inquiries. The accuracy, comprehensiveness, and clinical applicability of AI-generated responses were systematically analyzed.</p><p><strong>Methods: </strong>Frequently asked questions (FAQs) regarding priapism were collected from medical guidelines, literature, and online health platforms. Each AI model generated responses, which were independently assessed by two experts based on accuracy, fluency, and clinical relevance. The Global Quality Score (GQS) was used for evaluation. Statistical analysis was performed using one-way ANOVA, with a significance threshold of p<0.05.</p><p><strong>Results: </strong>ChatGPT and Gemini demonstrated comparable performance across all thematic categories, with mean scores ranging from 4.5-4.9, while Copilot showed significantly lower scores (3.2-4.2, p<0.001). Both ChatGPT and Gemini provided clinically relevant and accurate information, whereas Copilot's responses frequently lacked guideline-based recommendations.</p><p><strong>Conclusions: </strong>ChatGPT and Gemini were statistically comparable in generating reliable, clinically useful responses, making them valuable tools for medical education and patient counseling. Copilot, however, exhibited lower accuracy and applicability. These findings highlight the need for continuous refinement of AI models to enhance their role in clinical decision-making while ensuring human expertise remains central to patient care.</p>","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Agustin Perez-Londoño, Sumedh Kaul, Aaron Fleishman, Ruslan Korets, Heidi Rayala, Peter Chang, Andrew Wagner, Joaquim Bellmunt, Aria F Olumi, Boris Gershman
Introduction: High-grade T1 (HGT1) bladder cancer is considered to have high five-year recurrence and progression rates, at 50-70% and 25-50%, respectively; however, contemporary data are lacking. We examined the contemporary outcomes of HGT1 bladder cancer to inform patient counseling, management, and clinical trial design.
Methods: We identified patients aged ≥18 years with a new diagnosis of HGT1 bladder cancer between 2010 and 2022 treated at our institution. Recurrence-free (RFS), progression-free (PFS), and cancer-specific (CSS) survival were estimated using the Kaplan-Meier method. Associations of baseline characteristics with outcomes were evaluated using Cox regression.
Results: A total of 213 patients were included, representing 332 cancer occurrences. Median age at diagnosis was 72 (interquartile range [IQR] 65-80) years. Median followup for RFS, PFS, and CSS was 13, 20, and 36 months, respectively. The one-, three-, and five-year event-free rates were 65%, 51%, and 48% for RFS; 85%, 78%, and 72% for PFS; and 99%, 95%, and 95% for CSS. There was a median of 1 (IQR 1-2) recurrence per patient, with a median time to first recurrence of seven months (IQR 4-14) and a median time between recurrences of seven months (IQR 5-18). Larger tumor size was associated with increased risks of recurrence. Receipt of adjuvant intravesical therapy was associated with reduced risks of recurrence and progression.
Conclusions: Contemporary five-year recurrence and progression rates for HGT1 bladder cancer remain high at 53% and 28%, respectively. The disease burden is substantial, with a median time between recurrences of seven months. These results can inform patient counseling, management, and clinical trial design.
{"title":"Contemporary outcomes and disease burden of high-grade T1 bladder cancer.","authors":"Agustin Perez-Londoño, Sumedh Kaul, Aaron Fleishman, Ruslan Korets, Heidi Rayala, Peter Chang, Andrew Wagner, Joaquim Bellmunt, Aria F Olumi, Boris Gershman","doi":"10.5489/cuaj.9329","DOIUrl":"https://doi.org/10.5489/cuaj.9329","url":null,"abstract":"<p><strong>Introduction: </strong>High-grade T1 (HGT1) bladder cancer is considered to have high five-year recurrence and progression rates, at 50-70% and 25-50%, respectively; however, contemporary data are lacking. We examined the contemporary outcomes of HGT1 bladder cancer to inform patient counseling, management, and clinical trial design.</p><p><strong>Methods: </strong>We identified patients aged ≥18 years with a new diagnosis of HGT1 bladder cancer between 2010 and 2022 treated at our institution. Recurrence-free (RFS), progression-free (PFS), and cancer-specific (CSS) survival were estimated using the Kaplan-Meier method. Associations of baseline characteristics with outcomes were evaluated using Cox regression.</p><p><strong>Results: </strong>A total of 213 patients were included, representing 332 cancer occurrences. Median age at diagnosis was 72 (interquartile range [IQR] 65-80) years. Median followup for RFS, PFS, and CSS was 13, 20, and 36 months, respectively. The one-, three-, and five-year event-free rates were 65%, 51%, and 48% for RFS; 85%, 78%, and 72% for PFS; and 99%, 95%, and 95% for CSS. There was a median of 1 (IQR 1-2) recurrence per patient, with a median time to first recurrence of seven months (IQR 4-14) and a median time between recurrences of seven months (IQR 5-18). Larger tumor size was associated with increased risks of recurrence. Receipt of adjuvant intravesical therapy was associated with reduced risks of recurrence and progression.</p><p><strong>Conclusions: </strong>Contemporary five-year recurrence and progression rates for HGT1 bladder cancer remain high at 53% and 28%, respectively. The disease burden is substantial, with a median time between recurrences of seven months. These results can inform patient counseling, management, and clinical trial design.</p>","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mehmet Sefa Altay, Tugay Aksakalli, Ahmet Emre Cinislioğlu, Fevzi Bedir, Hüseyin Kocatürk, İbrahim Karabulut, Hüseyin Koçakgöl, Adem Utlu, Emre Şam, Şaban Oğuz Demirdöğen, İsa Özbey
Introduction: Erectile dysfunction (ED) is a significant issue that adversely affects the quality of life in young men. Venous leakage is a common etiologic factors of ED. This study aimed to evaluate the clinical efficacy and safety of venous ligation applied to incidentally detected dorsal penile vein anomalies during penoscrotal surgeries.
Methods: The study included 32 young male patients who presented with ED and underwent surgery for penoscrotal pathology (e.g., varicocele, hydrocele, spermatocele), during which an isolated dorsal penile vein anomaly was concurrently ligated. Patients were assessed preoperatively and at three and six months postoperatively using the International Index of Erectile Function (IIEF-5). Postoperative erectile response, patient satisfaction, and the presence of complications were also evaluated.
Results: The mean age was 33.1±5.4 years. The median operative time was 20 minutes (18-25), and the median followup duration was six months (6-9). The median IIEF-5 score increased from 18 (17-19) preoperatively to 21 (20-22) at three months and 22 (22-24) at six months (p1<0.001, p2<0.001, p3<0.001). Patient satisfaction improved significantly, with median satisfaction scores of 8 (8-9) at three months and 9 (8-10) at six months (p3<0.001). The need for PDE5i therapy decreased markedly, from 100% preoperatively to 56.2% at three months and 31.3% at six months (p1<0.001, p2<0.001, p3<0.001). No perioperative or postoperative complications were recorded.
Conclusions: Venous ligation applied to incidentally detected dorsal penile vein anomalies during penoscrotal surgeries represents an effective and reliable therapeutic option for young patients with ED.
{"title":"The impact of venous ligation on erectile dysfunction in young patients with an abnormal dorsal penile vein: Clinical outcomes of a novel surgical procedure.","authors":"Mehmet Sefa Altay, Tugay Aksakalli, Ahmet Emre Cinislioğlu, Fevzi Bedir, Hüseyin Kocatürk, İbrahim Karabulut, Hüseyin Koçakgöl, Adem Utlu, Emre Şam, Şaban Oğuz Demirdöğen, İsa Özbey","doi":"10.5489/cuaj.9357","DOIUrl":"https://doi.org/10.5489/cuaj.9357","url":null,"abstract":"<p><strong>Introduction: </strong>Erectile dysfunction (ED) is a significant issue that adversely affects the quality of life in young men. Venous leakage is a common etiologic factors of ED. This study aimed to evaluate the clinical efficacy and safety of venous ligation applied to incidentally detected dorsal penile vein anomalies during penoscrotal surgeries.</p><p><strong>Methods: </strong>The study included 32 young male patients who presented with ED and underwent surgery for penoscrotal pathology (e.g., varicocele, hydrocele, spermatocele), during which an isolated dorsal penile vein anomaly was concurrently ligated. Patients were assessed preoperatively and at three and six months postoperatively using the International Index of Erectile Function (IIEF-5). Postoperative erectile response, patient satisfaction, and the presence of complications were also evaluated.</p><p><strong>Results: </strong>The mean age was 33.1±5.4 years. The median operative time was 20 minutes (18-25), and the median followup duration was six months (6-9). The median IIEF-5 score increased from 18 (17-19) preoperatively to 21 (20-22) at three months and 22 (22-24) at six months (p1<0.001, p2<0.001, p3<0.001). Patient satisfaction improved significantly, with median satisfaction scores of 8 (8-9) at three months and 9 (8-10) at six months (p3<0.001). The need for PDE5i therapy decreased markedly, from 100% preoperatively to 56.2% at three months and 31.3% at six months (p1<0.001, p2<0.001, p3<0.001). No perioperative or postoperative complications were recorded.</p><p><strong>Conclusions: </strong>Venous ligation applied to incidentally detected dorsal penile vein anomalies during penoscrotal surgeries represents an effective and reliable therapeutic option for young patients with ED.</p>","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Wyatt MacNevin, Dara Liu, Robert Fraser, Karen Milford, Daniel T Keefe
{"title":"Case - Pediatric ureteropelvic junction obstruction leading to emphysematous pyelonephritis: A rare presentation of a life-threatening condition.","authors":"Wyatt MacNevin, Dara Liu, Robert Fraser, Karen Milford, Daniel T Keefe","doi":"10.5489/cuaj.9352","DOIUrl":"https://doi.org/10.5489/cuaj.9352","url":null,"abstract":"","PeriodicalId":50613,"journal":{"name":"Cuaj-Canadian Urological Association Journal","volume":" ","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}