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Complete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report 完全性阴道横隔并发脓瘘、原发性膀胱输尿管反流和异位输尿管伴肾丢失1例
IF 0.5
Urology Case Reports Pub Date : 2025-05-28 DOI: 10.1016/j.eucr.2025.103081
Izadora Gabriela Coutinho , Paulo Acácio Egger , Ailton Fernandes Junior , Angelo Cezar Bolognese Junior , Abikeilla Ariane Bomfim Gomes Bernardi , Amanda Yumi Ono Valderrama
{"title":"Complete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report","authors":"Izadora Gabriela Coutinho ,&nbsp;Paulo Acácio Egger ,&nbsp;Ailton Fernandes Junior ,&nbsp;Angelo Cezar Bolognese Junior ,&nbsp;Abikeilla Ariane Bomfim Gomes Bernardi ,&nbsp;Amanda Yumi Ono Valderrama","doi":"10.1016/j.eucr.2025.103081","DOIUrl":"10.1016/j.eucr.2025.103081","url":null,"abstract":"<div><div>A transverse vaginal septum is a rare Müllerian anomaly caused by incomplete fusion between the Müllerian ducts and the urogenital sinus. It can obstruct menstrual flow, leading to hematocolpos, hydrocolpos, or pyocolpos. We report a 12-year-old girl with recurrent hematocolpos, abdominal pain, urinary symptoms, and infections. Imaging showed a complete transverse vaginal septum and grade II vesicoureteral reflux. She underwent surgical drainage, septum resection, and ureteral reimplantation. Recovery was favorable, with symptom resolution and preserved renal function. This case emphasizes the need for early diagnosis and a multidisciplinary approach to avoid long-term complications in complex urogenital anomalies.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103081"},"PeriodicalIF":0.5,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144190199","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary renal parenchymal squamous cell carcinoma involving the renal pelvis: a case report and review of the literature 原发性肾实质鳞状细胞癌累及肾盂1例报告及文献复习
IF 0.5
Urology Case Reports Pub Date : 2025-05-28 DOI: 10.1016/j.eucr.2025.103083
Junjun Wu , Lei Wang , Pengpeng Zhao , Fuxiang Lin , Zhanping Xu
{"title":"Primary renal parenchymal squamous cell carcinoma involving the renal pelvis: a case report and review of the literature","authors":"Junjun Wu ,&nbsp;Lei Wang ,&nbsp;Pengpeng Zhao ,&nbsp;Fuxiang Lin ,&nbsp;Zhanping Xu","doi":"10.1016/j.eucr.2025.103083","DOIUrl":"10.1016/j.eucr.2025.103083","url":null,"abstract":"<div><div>Primary squamous cell carcinoma (SCC) of the renal parenchyma represents an exceptionally rare malignancy. We present an SCC case demonstrating renal pelvis invasion, histopathologically confirmed following radical nephrectomy. Postoperative adjuvant chemotherapy was initiated, with subsequent development of pulmonary and adrenal metastases at the 10th-month follow-up. After treatment adjustment, the patient is currently 12 months after the operation and is in good general condition. This case illustrates that a definitive diagnosis of primary renal parenchymal SCC remains achievable despite concomitant renal pelvis involvement, emphasizing the importance of comprehensive histopathological evaluation in such rare presentations.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103083"},"PeriodicalIF":0.5,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Isolated testicular metastasis from prostate cancer following three years of hormone therapy and radiotherapy 经过3年的激素治疗和放射治疗的前列腺癌的分离睾丸转移
IF 0.5
Urology Case Reports Pub Date : 2025-05-27 DOI: 10.1016/j.eucr.2025.103080
Ali Tabibi, Mohammad Sajjad Zabihi, Mahyar Najarian, Mehdi Dadpour
{"title":"Isolated testicular metastasis from prostate cancer following three years of hormone therapy and radiotherapy","authors":"Ali Tabibi,&nbsp;Mohammad Sajjad Zabihi,&nbsp;Mahyar Najarian,&nbsp;Mehdi Dadpour","doi":"10.1016/j.eucr.2025.103080","DOIUrl":"10.1016/j.eucr.2025.103080","url":null,"abstract":"<div><div>This case report presents a 61-year-old male patient diagnosed with high-risk prostate cancer who underwent hormone therapy and radiotherapy. Three years after beginning treatment, rising prostate-specific antigen (PSA) levels led to a PET CT scan, which identified isolated metastases in the left testicle. The patient then underwent a radical orchiectomy. One-year follow up revealed undetectable PSA and no evidence of any metastases. The significance of this case lies in the uncommon occurrence of testicular metastasis from prostate cancer, particularly when presenting in isolation after a prolonged period following hormone therapy and radiotherapy.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103080"},"PeriodicalIF":0.5,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167153","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute renal failure in the setting of bilateral ureteral obstruction secondary to plasmacytoid variant urothelial cell carcinoma 浆细胞样变尿路上皮细胞癌继发于双侧输尿管梗阻的急性肾功能衰竭
IF 0.5
Urology Case Reports Pub Date : 2025-05-27 DOI: 10.1016/j.eucr.2025.103084
Madison Dale , Claudia Studebaker-DeMartino , Rocco Morabito Jr. , Vincent Graffeo
{"title":"Acute renal failure in the setting of bilateral ureteral obstruction secondary to plasmacytoid variant urothelial cell carcinoma","authors":"Madison Dale ,&nbsp;Claudia Studebaker-DeMartino ,&nbsp;Rocco Morabito Jr. ,&nbsp;Vincent Graffeo","doi":"10.1016/j.eucr.2025.103084","DOIUrl":"10.1016/j.eucr.2025.103084","url":null,"abstract":"<div><div>Plasmacytoid urothelial carcinoma (PUC) is an aggressive variant of urothelial cell carcinoma (UCC) that has a tendency for unique presentation at time of diagnosis. We present a 68-year-old male who developed generalized abdominal pain with an incidental finding of acute renal failure secondary to ureteral strictures. He was subsequently diagnosed with PUC. Management of PUC is multifactorial with neoadjuvant chemotherapy followed by radical cystectomy. Despite these invasive treatments, the prognosis is often significantly inferior to typical UCC. This case demonstrates the need for high clinical suspicion in the setting of unpredicted strictures within the abdomen and pelvis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103084"},"PeriodicalIF":0.5,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144178213","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vacuum-assisted mini-ECIRS for calyceal diverticular stones in a recipient of a kidney transplant: A case report 真空辅助微型ecirs治疗肾移植受者肾盏憩室结石一例报告
IF 0.5
Urology Case Reports Pub Date : 2025-05-27 DOI: 10.1016/j.eucr.2025.103079
Ponthakorn Srithongsongsaeng, Kun Sirisopana, Surawach Piyawannarat, Yada Phengsalae, Premsant Sangkum, Wisoot Kongchareonsombat, Chinnakhet Ketsuwan
{"title":"Vacuum-assisted mini-ECIRS for calyceal diverticular stones in a recipient of a kidney transplant: A case report","authors":"Ponthakorn Srithongsongsaeng,&nbsp;Kun Sirisopana,&nbsp;Surawach Piyawannarat,&nbsp;Yada Phengsalae,&nbsp;Premsant Sangkum,&nbsp;Wisoot Kongchareonsombat,&nbsp;Chinnakhet Ketsuwan","doi":"10.1016/j.eucr.2025.103079","DOIUrl":"10.1016/j.eucr.2025.103079","url":null,"abstract":"<div><div>Urolithiasis in renal allografts can cause serious complications, particularly when involving calyceal diverticula due to altered anatomy. We report the case of a 44-year-old female recipient of a kidney transplant who presented with recurrent urinary tract infections and elevated serum creatinine levels. Imaging revealed a calyceal diverticular stone. After a failed retrograde approach, she underwent vacuum-assisted mini-endoscopic combined intrarenal surgery (ECIRS). A flexible ureteroscope enabled precise puncture and direct visualization for diverticular neck incision and fulguration. The procedure was successful with no complications. Vacuum-assisted mini-ECIRS is a safe and effective option for complex stone cases in recipients of transplants.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103079"},"PeriodicalIF":0.5,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spontaneous bladder perforation with urinary ascites secondary to posterior urethral valves and suspected atypical congenital nephrotic syndrome of a premature neonate: A case report 早产儿自发性膀胱穿孔伴后尿道瓣膜继发尿性腹水1例，疑为不典型先天性肾病综合征
IF 0.5
Urology Case Reports Pub Date : 2025-05-24 DOI: 10.1016/j.eucr.2025.103078
Alicia Phillips , Miranda Floen , Teri Mauch , Claudia Berrondo
{"title":"Spontaneous bladder perforation with urinary ascites secondary to posterior urethral valves and suspected atypical congenital nephrotic syndrome of a premature neonate: A case report","authors":"Alicia Phillips ,&nbsp;Miranda Floen ,&nbsp;Teri Mauch ,&nbsp;Claudia Berrondo","doi":"10.1016/j.eucr.2025.103078","DOIUrl":"10.1016/j.eucr.2025.103078","url":null,"abstract":"<div><div>Fetal bladder rupture is a rare phenomenon with few reported cases in the literature. It is often a complication of congenital abnormalities causing urinary obstruction, such as posterior urethral valves (PUV). Congenital nephrotic syndrome (CNS) is another rare genitourinary disorder characterized by proteinuria, hypoalbuminemia and edema presenting in the first 3 months of life. We present a case of a premature male infant delivered at 32 weeks with fetal ascites from bladder rupture secondary to PUV. The infant also exhibited clinical features suggestive of CNS. This case illustrates the value of comprehensive differential diagnosis, medical decision making, and collaborative multidisciplinary care.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103078"},"PeriodicalIF":0.5,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144138433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome 一例meyer - rokitansky - kuster - hauser综合征患者的直肠阴道瘘
IF 0.5
Urology Case Reports Pub Date : 2025-05-21 DOI: 10.1016/j.eucr.2025.103075
Puvvada Sandeep, S. Shanthakumar, Venkata Mahesh Chalumuru, D. Ramesh, Tarun Dilip Javali
{"title":"Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome","authors":"Puvvada Sandeep,&nbsp;S. Shanthakumar,&nbsp;Venkata Mahesh Chalumuru,&nbsp;D. Ramesh,&nbsp;Tarun Dilip Javali","doi":"10.1016/j.eucr.2025.103075","DOIUrl":"10.1016/j.eucr.2025.103075","url":null,"abstract":"<div><div>MRKH syndrome is defined by the congenital absence of the uterus and the upper two-thirds of the vagina in females, who otherwise exhibit normal secondary sexual characteristics and possess a typical 46, XX karyotype. Here we report a case of 23 year old female diagnosed with Mayer-Rokitansky-Kuster-Hauser syndrome when presenting with features of rectovaginal fistula.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103075"},"PeriodicalIF":0.5,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144147087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report 迟发不完全膀胱重复：意外误诊罕见病例报告
IF 0.5
Urology Case Reports Pub Date : 2025-05-19 DOI: 10.1016/j.eucr.2025.103074
Aya Mohamed Nasr Ibrahim , Mohab Alsaid Saad , Mustafa I. Al-Shalah , Zaid F. Altawallbeh , Abdelrahman Elkhiat , Mohamed Elsaqa , Hasan Ahmad Matar , Akhmad Asaad Matar , Mostafa Said
{"title":"Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report","authors":"Aya Mohamed Nasr Ibrahim ,&nbsp;Mohab Alsaid Saad ,&nbsp;Mustafa I. Al-Shalah ,&nbsp;Zaid F. Altawallbeh ,&nbsp;Abdelrahman Elkhiat ,&nbsp;Mohamed Elsaqa ,&nbsp;Hasan Ahmad Matar ,&nbsp;Akhmad Asaad Matar ,&nbsp;Mostafa Said","doi":"10.1016/j.eucr.2025.103074","DOIUrl":"10.1016/j.eucr.2025.103074","url":null,"abstract":"<div><div>Incomplete bladder duplication (BD) is a rare congenital anomaly in which two bladder halves remain partially connected and share a single urethra; only 12 cases have been recorded. A 60-year-old female with severe lower urinary tract symptoms (LUTS) following hysterectomy and sacrocolpopexy. Initially suspected to be mesh-related, cystourethroscopy and MRI revealed an incomplete sagittal bladder septum. Laser excision resolved her symptoms. While surgery is rarely needed for BD, this case underscores its necessity in symptomatic patients. This case of incomplete BD without associated multiple congenital malformations emphasizes the need to consider rare congenital anomalies even in atypical presentation.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103074"},"PeriodicalIF":0.5,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144178212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful healing of a suprapubic and inguinal necrotizing fasciitis in an 18-month-old girl using sugar dressings: A case report 糖敷料治疗18个月女童耻骨上及腹股沟坏死性筋膜炎1例
IF 0.5
Urology Case Reports Pub Date : 2025-05-19 DOI: 10.1016/j.eucr.2025.103073
Roland Muyisa , Emile Watumwa , Charmante Pendeza , Angelique Makelele , Marina Maha , Pascal Kalondero
{"title":"Successful healing of a suprapubic and inguinal necrotizing fasciitis in an 18-month-old girl using sugar dressings: A case report","authors":"Roland Muyisa ,&nbsp;Emile Watumwa ,&nbsp;Charmante Pendeza ,&nbsp;Angelique Makelele ,&nbsp;Marina Maha ,&nbsp;Pascal Kalondero","doi":"10.1016/j.eucr.2025.103073","DOIUrl":"10.1016/j.eucr.2025.103073","url":null,"abstract":"<div><div>Necrotizing fasciitis (NF) is a severe infection, rare in pediatrics, often challenging to diagnose. An 18-month-old girl presented with fever and swelling after a minor cut. Over six days, her condition worsened, leading to the diagnosis of NF. Surgical debridement revealed extensive necrosis. After intensive care with sugar dressings and broad-spectrum antibiotics, her wound improved significantly. She was discharged after 21 days, emphasizing the importance of hygiene and timely medical care.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103073"},"PeriodicalIF":0.5,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144107936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful living donor kidney transplantation following ex vivo repair of renal artery aneurysm 肾动脉瘤体外修复后活体肾移植成功
IF 0.5
Urology Case Reports Pub Date : 2025-05-19 DOI: 10.1016/j.eucr.2025.103076
Daniel Alejandro Arreola-Ramírez , Sahara Hurtado-Gómez , Alec Anceno , Fernando Fernández Varela-Gómez , Nancy Berenice Guzmán-Martínez , Hirepan Armenta-Álvarez , Alan Gabriel Contreras-Saldívar
{"title":"Successful living donor kidney transplantation following ex vivo repair of renal artery aneurysm","authors":"Daniel Alejandro Arreola-Ramírez ,&nbsp;Sahara Hurtado-Gómez ,&nbsp;Alec Anceno ,&nbsp;Fernando Fernández Varela-Gómez ,&nbsp;Nancy Berenice Guzmán-Martínez ,&nbsp;Hirepan Armenta-Álvarez ,&nbsp;Alan Gabriel Contreras-Saldívar","doi":"10.1016/j.eucr.2025.103076","DOIUrl":"10.1016/j.eucr.2025.103076","url":null,"abstract":"<div><div>Renal-artery aneurysms (RAA), rare vascular lesions (≈0.1 % prevalence), may be detected during living-donor evaluations. We report a successful right kidney transplant from a 33-year-old woman with an 11 × 13 mm saccular RAA at the first bifurcation, detected by CT angiography. Following hand-assisted laparoscopic nephrectomy, ex vivo repair involved aneurysm excision and reconstruction with a 6-mm heparin-bonded ePTFE graft. Cold ischemia was 110 min; implantation into the 69-year-old recipient was uneventful. Immediate postoperative diuresis occurred; discharge creatinine was 1.2 mg/dL. At 18 months, both remain asymptomatic with stable renal function and normotension.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103076"},"PeriodicalIF":0.5,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144114833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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