Inflammatory myofibroblastic tumor(IMT) is an uncommon soft tissue neoplasm rarely reported in the urinary tract. A 54-year-old male presented to our institution with low back and abdominal pain, hematuria, and lower urinary tract symptoms for 2 months. We performed abdominal contrast-enhanced computed tomography (CT) and magnetic resonance imaging (MRI), which showed a mass in the right renal pelvis-inferior calyx. Then, we performed the laparoscopic radical nephroureterectomy.
{"title":"Inflammatory myofibroblastic tumor of the right renal pelvis: A case report","authors":"Xiaorui Zhu, Xueli Dong, Hongzhou Sheng, Renbin Deng, Xianzhong Duan","doi":"10.1016/j.eucr.2025.102969","DOIUrl":"10.1016/j.eucr.2025.102969","url":null,"abstract":"<div><div>Inflammatory myofibroblastic tumor(IMT) is an uncommon soft tissue neoplasm rarely reported in the urinary tract. A 54-year-old male presented to our institution with low back and abdominal pain, hematuria, and lower urinary tract symptoms for 2 months. We performed abdominal contrast-enhanced computed tomography (CT) and magnetic resonance imaging (MRI), which showed a mass in the right renal pelvis-inferior calyx. Then, we performed the laparoscopic radical nephroureterectomy.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102969"},"PeriodicalIF":0.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143373078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-29DOI: 10.1016/j.eucr.2025.102962
Sarah Cairo, Gabriella Grisotti, Hanmin Lee
Incomplete obliteration of the allantois during development gives rise to urachal remnants. Presentation is variable and can range from draining umbilicus to chronic granuloma to acute infection requiring management with antibiotics and surgical excision. High index of suspicion is required to diagnoses more unusual presentations. This is a report on a case of urachal remnant presenting as a suprapubic sinus in a pediatric patient.
{"title":"Rare presentation of urachal remnant with suprapubic sinus: A case report","authors":"Sarah Cairo, Gabriella Grisotti, Hanmin Lee","doi":"10.1016/j.eucr.2025.102962","DOIUrl":"10.1016/j.eucr.2025.102962","url":null,"abstract":"<div><div>Incomplete obliteration of the allantois during development gives rise to urachal remnants. Presentation is variable and can range from draining umbilicus to chronic granuloma to acute infection requiring management with antibiotics and surgical excision. High index of suspicion is required to diagnoses more unusual presentations. This is a report on a case of urachal remnant presenting as a suprapubic sinus in a pediatric patient.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102962"},"PeriodicalIF":0.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137792","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-28DOI: 10.1016/j.eucr.2025.102963
Shang Xu, Xinning Wang, Wei Jiao
Prostate stromal sarcoma is very rare among patients with prostate cancer, accounting for <0.1 % of prostate malignancy. Here, we report a case of prostate stromal sarcoma combined with incidental adenocarcinoma with normal serum PSA after radical prostatectomy. This case is unique in that the occurrence of incidental adenocarcinoma might interfere with the postoperative follow-up and treatment. We can only draw from the experiences of case reports and retrospective analysis. This article describes a presentation of a rare tumor case and a review of the literature.
{"title":"A case of stromal sarcoma of the prostate with the incidental detection of prostate adenocarcinoma","authors":"Shang Xu, Xinning Wang, Wei Jiao","doi":"10.1016/j.eucr.2025.102963","DOIUrl":"10.1016/j.eucr.2025.102963","url":null,"abstract":"<div><div>Prostate stromal sarcoma is very rare among patients with prostate cancer, accounting for <0.1 % of prostate malignancy. Here, we report a case of prostate stromal sarcoma combined with incidental adenocarcinoma with normal serum PSA after radical prostatectomy. This case is unique in that the occurrence of incidental adenocarcinoma might interfere with the postoperative follow-up and treatment. We can only draw from the experiences of case reports and retrospective analysis. This article describes a presentation of a rare tumor case and a review of the literature.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102963"},"PeriodicalIF":0.5,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-25DOI: 10.1016/j.eucr.2025.102944
Haidong Yang , Wenli Yang , Nanjun Duan , Jing Luo , Zhengyan Yang , Weiran Zhang , Wei Feng , Haifeng Wang
Renal pelvic cancer is relatively rare in clinical practice, and renal pelvic cancer characterized by renal infarction is even rarer. We here report a case of renal pelvic urothelial carcinoma with squamous metaplasia with renal infarction as the main imaging feature, and summarize the imaging manifestations of some rare renal pelvic carcinomas.
Conclusion
The imaging features of renal pelvis cancer are diverse and often confused with some benign and malignant diseases, suggesting that extra caution should be exercised in the diagnosis and treatment of renal pelvis cancer.
{"title":"Renal pelvic urothelial carcinoma with imaging features presenting as renal infarction 1 case report and literature review","authors":"Haidong Yang , Wenli Yang , Nanjun Duan , Jing Luo , Zhengyan Yang , Weiran Zhang , Wei Feng , Haifeng Wang","doi":"10.1016/j.eucr.2025.102944","DOIUrl":"10.1016/j.eucr.2025.102944","url":null,"abstract":"<div><div>Renal pelvic cancer is relatively rare in clinical practice, and renal pelvic cancer characterized by renal infarction is even rarer. We here report a case of renal pelvic urothelial carcinoma with squamous metaplasia with renal infarction as the main imaging feature, and summarize the imaging manifestations of some rare renal pelvic carcinomas.</div></div><div><h3>Conclusion</h3><div>The imaging features of renal pelvis cancer are diverse and often confused with some benign and malignant diseases, suggesting that extra caution should be exercised in the diagnosis and treatment of renal pelvis cancer.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102944"},"PeriodicalIF":0.5,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143349261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-24DOI: 10.1016/j.eucr.2025.102947
Basmah Al Ghanim , Mohammed Al Bagshi , Faisal Altwijri , Basim Al Baqawi , Mahmoud Trbay
Urethral polyps are rare benign lesions causing urinary tract obstruction in pediatric patients, predominantly affecting males. They arise from the posterior urethra in males and mid-urethra in females.
An 11-day-old male with antenatal hydronephrosis presented with UTI. Imaging revealed bilateral grade II hydronephrosis, distended bladder, and grade 5 bilateral vesicoureteral reflux. A fibroepithelial urethral polyp was identified and treated with bipolar resection.
Postoperative evaluation showed complete resolution of symptoms, emphasizing the importance of comprehensive urological evaluation in neonates with antenatal hydronephrosis.
{"title":"Fibroepithelial urethral polyp causing complex urinary tract obstruction in a neonate: A rare case report and management","authors":"Basmah Al Ghanim , Mohammed Al Bagshi , Faisal Altwijri , Basim Al Baqawi , Mahmoud Trbay","doi":"10.1016/j.eucr.2025.102947","DOIUrl":"10.1016/j.eucr.2025.102947","url":null,"abstract":"<div><div>Urethral polyps are rare benign lesions causing urinary tract obstruction in pediatric patients, predominantly affecting males. They arise from the posterior urethra in males and mid-urethra in females.</div><div>An 11-day-old male with antenatal hydronephrosis presented with UTI. Imaging revealed bilateral grade II hydronephrosis, distended bladder, and grade 5 bilateral vesicoureteral reflux. A fibroepithelial urethral polyp was identified and treated with bipolar resection.</div><div>Postoperative evaluation showed complete resolution of symptoms, emphasizing the importance of comprehensive urological evaluation in neonates with antenatal hydronephrosis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102947"},"PeriodicalIF":0.5,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-23DOI: 10.1016/j.eucr.2025.102961
Eltahir Ahmed Eltahir , Ghassan Mahmoud Mohammed Yousuf , Walyeldin Elnour Mohamed Elfakey , Moneer Ali Abdallah , Muna Mohammed Ahmed Hamid Ahmed
Introduction
Chyluria is characterized by the passage of milky urine resulting from abnormal lymphatic drainage into the urinary tract. In parasitic cases, it is commonly caused by Wuchereria bancrofti and has varying severities. Diagnosis relies on clinical, laboratory, and radiological assessments, with treatment options spanning dietary modifications to surgical interventions.
Case presentation
A 43-year-old male presented with chyluria for one year. He received medical treatment for filariasis without response. sclerotherapy with 5 % povidone Iodine was done successfully.
Conclusion
Severe cases of chyluria can be treated successfully with povidone Iodine 5 %.
{"title":"Severe filarial chyluria Managed successfully with sclerotherapy: A case report from Sudan","authors":"Eltahir Ahmed Eltahir , Ghassan Mahmoud Mohammed Yousuf , Walyeldin Elnour Mohamed Elfakey , Moneer Ali Abdallah , Muna Mohammed Ahmed Hamid Ahmed","doi":"10.1016/j.eucr.2025.102961","DOIUrl":"10.1016/j.eucr.2025.102961","url":null,"abstract":"<div><h3>Introduction</h3><div>Chyluria is characterized by the passage of milky urine resulting from abnormal lymphatic drainage into the urinary tract. In parasitic cases, it is commonly caused by Wuchereria bancrofti and has varying severities. Diagnosis relies on clinical, laboratory, and radiological assessments, with treatment options spanning dietary modifications to surgical interventions.</div></div><div><h3>Case presentation</h3><div>A 43-year-old male presented with chyluria for one year. He received medical treatment for filariasis without response. sclerotherapy with 5 % povidone Iodine was done successfully.</div></div><div><h3>Conclusion</h3><div>Severe cases of chyluria can be treated successfully with povidone Iodine 5 %.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102961"},"PeriodicalIF":0.5,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-22DOI: 10.1016/j.eucr.2025.102958
Mohammed Salah E. Khalifa Salem , Abdul Alherek , Daniel DaSilva , Jacob Varghese , Alain Mwamba Mukendi
Bilateral ureteropelvic junction obstruction resulting from distinct vascular anomalies on each side, with a pre-ureteric vena cava on the right and crossing vessels on the left, has not been previously documented in the literature. Even more intriguing is the association between a grade 3 hydronephrosis and a type 2 circumcaval ureter. This unprecedented report discusses this association and its management.
{"title":"Unprecedented Association: Bilateral UPJ obstruction with grade 3 hydronephrosis caused by Type 2 circumcaval right ureter and left lower pole crossing vessels","authors":"Mohammed Salah E. Khalifa Salem , Abdul Alherek , Daniel DaSilva , Jacob Varghese , Alain Mwamba Mukendi","doi":"10.1016/j.eucr.2025.102958","DOIUrl":"10.1016/j.eucr.2025.102958","url":null,"abstract":"<div><div>Bilateral ureteropelvic junction obstruction resulting from distinct vascular anomalies on each side, with a pre-ureteric vena cava on the right and crossing vessels on the left, has not been previously documented in the literature. Even more intriguing is the association between a grade 3 hydronephrosis and a type 2 circumcaval ureter. This unprecedented report discusses this association and its management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102958"},"PeriodicalIF":0.5,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.eucr.2025.102956
Marco Rosario, Jerome Kyle San Jose, David Ende
Traumatic testicular dislocation is a rare consequence of blunt scrotal injury. Testicular dislocation typically results from high-energy trauma, such as motor vehicle accidents or falls, leading to dislodgement of the testicle from its normal anatomical position. We present a rare case of a young man with traumatic unilateral dislocation and exteriorisation of the testicle through a sub corona penile defect, following a high-speed motorbike accident.
{"title":"Traumatic testicular dislocation and exteriorisation through penis: A case report","authors":"Marco Rosario, Jerome Kyle San Jose, David Ende","doi":"10.1016/j.eucr.2025.102956","DOIUrl":"10.1016/j.eucr.2025.102956","url":null,"abstract":"<div><div>Traumatic testicular dislocation is a rare consequence of blunt scrotal injury. Testicular dislocation typically results from high-energy trauma, such as motor vehicle accidents or falls, leading to dislodgement of the testicle from its normal anatomical position. We present a rare case of a young man with traumatic unilateral dislocation and exteriorisation of the testicle through a sub corona penile defect, following a high-speed motorbike accident.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102956"},"PeriodicalIF":0.5,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.eucr.2025.102959
Lauren Poniatowski , Raymond Tse , Caitlin Smith , Mike Tretiakov , Todd Blumberg , Margarett Shnorhavorian
We present the case of a newborn male with congenital amniotic band syndrome and a constriction band involving the right inguinal crease, scrotum and perineum. He was diagnosed prenatally and referred to our institution after developing a right femoral nerve palsy. Surgical management included excision of the constriction band and Z-plasty closure. We discuss the considerations for safe and cosmetic surgical outcomes in this rare presentation of amniotic band syndrome. A multidisciplinary approach to management is essential during workup and surgical intervention.
{"title":"Amniotic constriction band of the pelvis in a newborn male","authors":"Lauren Poniatowski , Raymond Tse , Caitlin Smith , Mike Tretiakov , Todd Blumberg , Margarett Shnorhavorian","doi":"10.1016/j.eucr.2025.102959","DOIUrl":"10.1016/j.eucr.2025.102959","url":null,"abstract":"<div><div>We present the case of a newborn male with congenital amniotic band syndrome and a constriction band involving the right inguinal crease, scrotum and perineum. He was diagnosed prenatally and referred to our institution after developing a right femoral nerve palsy. Surgical management included excision of the constriction band and Z-plasty closure. We discuss the considerations for safe and cosmetic surgical outcomes in this rare presentation of amniotic band syndrome. A multidisciplinary approach to management is essential during workup and surgical intervention.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102959"},"PeriodicalIF":0.5,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.eucr.2025.102957
Mohamed Ali Bedoui, Ahmed Saadi, Bourgou Ibrahim, Seif Mokadem, Amine Hermi, Bilel Saïdani, Haroun Ayed, Marouene Chakroun, Riadh Ben Slama
Solitary fibrous tumor (SFTs), initially described in the 1930s, are a group of rare heterogeneous tumors primarily located in the pleural area but can manifest in any site.This article focuses on the case of a patient with a localized retroperitoneal pubic tumor treated surgically, which demonstrates on one hand the heterogeneity of clinical manifestations, the limited diagnostic contribution of imaging, and on the other hand the histological diagnostic difficulty despite the recent contribution of immunohistochemistry. Management remains primarily surgical, to the detriment of other alternatives that have not yet shown encouraging results.
{"title":"Retro vesical solitary fibrous tumor: A case report","authors":"Mohamed Ali Bedoui, Ahmed Saadi, Bourgou Ibrahim, Seif Mokadem, Amine Hermi, Bilel Saïdani, Haroun Ayed, Marouene Chakroun, Riadh Ben Slama","doi":"10.1016/j.eucr.2025.102957","DOIUrl":"10.1016/j.eucr.2025.102957","url":null,"abstract":"<div><div>Solitary fibrous tumor (SFTs), initially described in the 1930s, are a group of rare heterogeneous tumors primarily located in the pleural area but can manifest in any site.This article focuses on the case of a patient with a localized retroperitoneal pubic tumor treated surgically, which demonstrates on one hand the heterogeneity of clinical manifestations, the limited diagnostic contribution of imaging, and on the other hand the histological diagnostic difficulty despite the recent contribution of immunohistochemistry. Management remains primarily surgical, to the detriment of other alternatives that have not yet shown encouraging results.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102957"},"PeriodicalIF":0.5,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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