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Urology Case Reports最新文献

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A high-grade undifferentiated prostate malignancy in a young male suggestive of male adnexal tumour of Wolffian origin – A rare case and diagnostic challenge 年轻男性的高级别未分化前列腺恶性肿瘤提示男性附件肿瘤的起源-一个罕见的病例和诊断的挑战
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-27 DOI: 10.1016/j.eucr.2026.103359
Rowan Klein Nulend , Kathleen Lockhart , Kevin Tree , Linh NK. Tran , Bashar Matti , Yelise Foon , Ali Moghimi , Daniel Wong , Jordan Butler , Lawrence HC. Kim , Audrey Wang , Manish I. Patel
{"title":"A high-grade undifferentiated prostate malignancy in a young male suggestive of male adnexal tumour of Wolffian origin – A rare case and diagnostic challenge","authors":"Rowan Klein Nulend ,&nbsp;Kathleen Lockhart ,&nbsp;Kevin Tree ,&nbsp;Linh NK. Tran ,&nbsp;Bashar Matti ,&nbsp;Yelise Foon ,&nbsp;Ali Moghimi ,&nbsp;Daniel Wong ,&nbsp;Jordan Butler ,&nbsp;Lawrence HC. Kim ,&nbsp;Audrey Wang ,&nbsp;Manish I. Patel","doi":"10.1016/j.eucr.2026.103359","DOIUrl":"10.1016/j.eucr.2026.103359","url":null,"abstract":"<div><div>We report a rare case of a high-grade, poorly differentiated prostatic malignancy in a 24-year-old, initially presenting with haematuria and urinary retention following trauma. Imaging and cystoscopy revealed a large prostate mass. Although a final histopathological diagnosis could not be definitively determined, expert review suggests this may resemble a male adnexal tumour of Wolffian origin, an extremely rare pathology. The patient underwent neoadjuvant chemotherapy, followed by radical cystoprostatectomy and adjuvant radiotherapy. He remains in remission 18 months post-treatment. This case underscores the importance of thorough investigation and multidisciplinary management of rare, aggressive prostatic tumours in young patients.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103359"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146188675","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
[A rare case of complex pyelocutaneous fistula following microwave ablation for recurrent renal cell carcinoma successfully managed with radical nephrectomy] 【微波消融治疗复发性肾癌合并根治性肾切除术成功治疗一例复杂肾盂皮瘘】
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-10 DOI: 10.1016/j.eucr.2026.103344
Lianpeng Gao , Bo Zhu , Xiaoxia Li , Yuyun Wu , Wenbo Zhou , Jiongming Li
{"title":"[A rare case of complex pyelocutaneous fistula following microwave ablation for recurrent renal cell carcinoma successfully managed with radical nephrectomy]","authors":"Lianpeng Gao ,&nbsp;Bo Zhu ,&nbsp;Xiaoxia Li ,&nbsp;Yuyun Wu ,&nbsp;Wenbo Zhou ,&nbsp;Jiongming Li","doi":"10.1016/j.eucr.2026.103344","DOIUrl":"10.1016/j.eucr.2026.103344","url":null,"abstract":"<div><div>A complex pyelocutaneous fistula developed after microwave ablation for recurrent clear cell renal carcinoma following partial nephrectomy. The fistula persisted despite prolonged drainage, antibiotics, ureteral stenting, and other conservative measures. Definitive management required laparoscopic radical nephrectomy with complete excision of the fistulous tract and involved psoas tissue. Histopathology showed chronic inflammation without residual malignancy. This case supports early consideration of radical nephrectomy for refractory, anatomically complex pyelocutaneous fistulas.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103344"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146038742","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
Recurrent bladder paraganglioma with peritoneal dissemination: An unusual pattern of metastatic progression. Case report and literature review 复发性膀胱副神经节瘤伴腹膜播散：一种不寻常的转移进展模式。病例报告及文献复习
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-10 DOI: 10.1016/j.eucr.2026.103342
Paolo Guedes Oliva , Pablo Jiménez Marrero , Rubén Espino Espino , Reinaldo Marrero Domínguez , Irene Expósito Remedios , Rafael Camacho Galán
{"title":"Recurrent bladder paraganglioma with peritoneal dissemination: An unusual pattern of metastatic progression. Case report and literature review","authors":"Paolo Guedes Oliva ,&nbsp;Pablo Jiménez Marrero ,&nbsp;Rubén Espino Espino ,&nbsp;Reinaldo Marrero Domínguez ,&nbsp;Irene Expósito Remedios ,&nbsp;Rafael Camacho Galán","doi":"10.1016/j.eucr.2026.103342","DOIUrl":"10.1016/j.eucr.2026.103342","url":null,"abstract":"<div><div>We report the case of a 26-year-old man diagnosed with multifocal bladder paraganglioma, an exceptionally rare neuroendocrine tumor. The patient presented with hypertension and adrenergic symptoms triggered by micturition, associated with elevated metanephrines and multiple pelvic lesions. He underwent complete laparoscopic resection, including partial cystectomy, achieving initial biochemical remission. Early local recurrence and subsequent peritoneal carcinomatosis<u>, an uncommon metastatic pattern,</u> were observed, requiring systemic therapy. This case highlights the diagnostic challenges, potential for aggressive behavior, and limited therapeutic options in metastatic bladder paraganglioma, underscoring the need for high clinical suspicion, adequate preoperative management, and long-term follow-up.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103342"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145980327","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
Solitary adrenal gland metastasis detected at 24-month follow-up for muscle-invasive bladder cancer 肌肉浸润性膀胱癌患者24个月随访发现单发肾上腺转移
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2025-12-30 DOI: 10.1016/j.eucr.2025.103334
Nicola Schiavone , Marco Finati , Anna Ricapito , Antonio Fanelli , Gaetano Valerio Palella , Ugo Giovanni Falagario , Luigi Cormio , Carlo Bettocchi , Gian Maria Busetto , Giuseppe Carrieri
{"title":"Solitary adrenal gland metastasis detected at 24-month follow-up for muscle-invasive bladder cancer","authors":"Nicola Schiavone ,&nbsp;Marco Finati ,&nbsp;Anna Ricapito ,&nbsp;Antonio Fanelli ,&nbsp;Gaetano Valerio Palella ,&nbsp;Ugo Giovanni Falagario ,&nbsp;Luigi Cormio ,&nbsp;Carlo Bettocchi ,&nbsp;Gian Maria Busetto ,&nbsp;Giuseppe Carrieri","doi":"10.1016/j.eucr.2025.103334","DOIUrl":"10.1016/j.eucr.2025.103334","url":null,"abstract":"<div><div>Solitary adrenal metastasis from bladder urothelial carcinoma is extremely uncommon. We report a 52-year-old man with high-grade pT3bN0R0 urothelial carcinoma of the bladder, who developed a <strong>solitary</strong> right adrenal metastasis (59 × 31 mm) 20 months after neoadjuvant chemotherapy and cystectomy (visible at the November 2024 CT, absent in March 2024). Surgical adrenalectomy was aborted due to adhesions and muscular invasion. After systemic therapy, the disease progressed with bilateral adrenal involvement. Adrenal metastases occur in 14 % of bladder cancer cases, isolated adrenal involvement is rare and aggressive; guidelines emphasise individualized multimodal management and suggest that earlier PET/CT may improve outcomes.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103334"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145897994","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
A rare entity in the retroperitoneum: Case report of a primary seminoma 腹膜后罕见肿瘤：原发性精原细胞瘤1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-02 DOI: 10.1016/j.eucr.2025.103335
Luowu Wang, Ke Yang, Chaojin Liang, Jun xing, Yao Bai
{"title":"A rare entity in the retroperitoneum: Case report of a primary seminoma","authors":"Luowu Wang,&nbsp;Ke Yang,&nbsp;Chaojin Liang,&nbsp;Jun xing,&nbsp;Yao Bai","doi":"10.1016/j.eucr.2025.103335","DOIUrl":"10.1016/j.eucr.2025.103335","url":null,"abstract":"<div><div>Primary retroperitoneal seminoma is an extremely rare extragonadal germ cell tumor. A 61-year-old male was referred following the discovery of a retroperitoneal mass on routine physical examination. Computed tomography and PET-CT revealed a soft-tissue nodule near the left renal hilum, suggestive of a neoplasm. The patient underwent surgical resection, and histopathology confirmed seminoma. Scrotal ultrasound showed no testicular abnormalities, thereby excluding a metastatic origin and confirming the diagnosis of primary retroperitoneal seminoma. This case underscores the importance of considering this rare entity in the differential diagnosis of retroperitoneal masses.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103335"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145898023","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
A case report: Synchronous occurrence of clear cell renal cell carcinoma and low-malignant-potential multicystic renal tumor within the same kidney 透明细胞肾细胞癌与低恶性潜能多囊肾肿瘤同时发生1例。
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-28 DOI: 10.1016/j.eucr.2026.103360
Chaojin Liang, Ke Yang, Jun Xing, Luowu Wang, Yao Bai, Yuanman Luo
{"title":"A case report: Synchronous occurrence of clear cell renal cell carcinoma and low-malignant-potential multicystic renal tumor within the same kidney","authors":"Chaojin Liang,&nbsp;Ke Yang,&nbsp;Jun Xing,&nbsp;Luowu Wang,&nbsp;Yao Bai,&nbsp;Yuanman Luo","doi":"10.1016/j.eucr.2026.103360","DOIUrl":"10.1016/j.eucr.2026.103360","url":null,"abstract":"<div><div>The simultaneous occurrence of different tumor types in the same kidney is relatively rare. This report describes a 76-year-old male patient presenting with concurrent clear cell renal cell carcinoma (ccRCC) and <u>multilocular cystic renal neoplasm of low malignant potential (MCRNLMP)</u> in a single kidney. CT imaging revealed a solid mass in the upper pole and a Bosniak III cyst in the lower pole. The patient underwent radical nephrectomy, and pathological examination confirmed the coexistence of both lesions. This highlights the limitations of imaging diagnosis and underscores the critical importance of histopathological diagnosis for treatment decision-making.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103360"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146167241","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
Management of a crochet hook penetrating perineal injury: A case report 钩针刺穿会阴伤1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2025-12-30 DOI: 10.1016/j.eucr.2025.103336
Asmelash Gebresilase Tewelde , Yirgalem Teklebirhan Gebreziher , Hadush Tesfay Negash , Birhane Mekonen Negash
{"title":"Management of a crochet hook penetrating perineal injury: A case report","authors":"Asmelash Gebresilase Tewelde ,&nbsp;Yirgalem Teklebirhan Gebreziher ,&nbsp;Hadush Tesfay Negash ,&nbsp;Birhane Mekonen Negash","doi":"10.1016/j.eucr.2025.103336","DOIUrl":"10.1016/j.eucr.2025.103336","url":null,"abstract":"<div><div>Removing an embedded barbed hook in the body without causing further tissue damage is a challenge in the emergency department (ED). A crochet hook is one of these barbed hooks.</div><div>A 6-year-old male child presented to our hospital after 1 hour of crochet hook needle injury to the perineum. On perineal examination there was a sharp material imbedded in the anterior perineal area on the right side from the medial raphe. His follow-up course was uneventful.</div><div>The advance-and-cut method is the most practiced and successful. The choice of management techniques depends on the anatomic location and depth of the hook.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103336"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145898040","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 angiosarcoma with renal vein thrombus: Case report and Review of literature 原发性肾血管肉瘤合并肾静脉血栓1例并文献复习
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-19 DOI: 10.1016/j.eucr.2026.103351
Mauricio S. Rodríguez-Mar , Jose Manuel Torres-Zazueta , Ricardo Fernández-Ferreira , Josué Farid Elías-Delgado , Luis A. Jiménez-López , Abel A. Ricardez-Espinosa , Mariana Hernández-Ramírez
{"title":"Primary renal angiosarcoma with renal vein thrombus: Case report and Review of literature","authors":"Mauricio S. Rodríguez-Mar ,&nbsp;Jose Manuel Torres-Zazueta ,&nbsp;Ricardo Fernández-Ferreira ,&nbsp;Josué Farid Elías-Delgado ,&nbsp;Luis A. Jiménez-López ,&nbsp;Abel A. Ricardez-Espinosa ,&nbsp;Mariana Hernández-Ramírez","doi":"10.1016/j.eucr.2026.103351","DOIUrl":"10.1016/j.eucr.2026.103351","url":null,"abstract":"<div><div>Primary angiosarcoma of the kidney is extremely rare and aggressive cancer when it presents renal vein thrombus. This presentation confers poor prognosis, with limited therapeutic options. We present a case that began with anemia and macroscopic hematuria. At diagnosis, computed tomography (CT) showed thrombosis of the left renal vein, and a radical nephrectomy was performed. Histological examination revealed a carcinoma of the collecting ducts of Bellini, with immunohistochemistry positive for epithelioid angiosarcoma.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103351"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146038743","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
Targeting mutant VHL-gene results in therapy response in metastatic clear cell carcinoma of rete testis 靶向突变vhl基因在睾丸网转移性透明细胞癌中的治疗效果。
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-02-16 DOI: 10.1016/j.eucr.2026.103376
Michael Karl Melzer , Angelika Mattigk , Verena I. Gaidzik , Nadine Therese Gaisa , Julia Schwenke , Friedemann Zengerling
{"title":"Targeting mutant VHL-gene results in therapy response in metastatic clear cell carcinoma of rete testis","authors":"Michael Karl Melzer ,&nbsp;Angelika Mattigk ,&nbsp;Verena I. Gaidzik ,&nbsp;Nadine Therese Gaisa ,&nbsp;Julia Schwenke ,&nbsp;Friedemann Zengerling","doi":"10.1016/j.eucr.2026.103376","DOIUrl":"10.1016/j.eucr.2026.103376","url":null,"abstract":"<div><div>Epididymal and rete testis tumors are exceedingly rare. We report a 69-year-old male who presented with progressive swelling of the right testis/epididymis; histopathology confirmed clear cell carcinoma of the rete testis. Staging with FDG-PET-CT revealed bilateral pulmonary metastases. Subsequent gene panel sequencing identified a pathogenic variant of <em>VHL</em> and a likely pathogenic variant of <em>TP53</em>. Off-label treatment with belzutifan was initiated. Regression of the pulmonary lesion with ongoing complete remission at 12 months of follow-up was observed. This case highlights the importance of molecular profiling for personalized therapy in rare tumor entities.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103376"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147310933","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
Bladder paraganglioma with lymph node metastasis treated by surgery with long-term recurrence-free survival: A case report 膀胱副神经节瘤伴淋巴结转移行手术治疗，长期无复发生存1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-02-06 DOI: 10.1016/j.eucr.2026.103363
Takanori Hayase , Hiroshi Takashima , Yohei Sawada , Riku Mitsui , Toshiki Tsuboi , Hirohiko Morimoto , Junichi Fukushima , Satoru Hayashi
{"title":"Bladder paraganglioma with lymph node metastasis treated by surgery with long-term recurrence-free survival: A case report","authors":"Takanori Hayase ,&nbsp;Hiroshi Takashima ,&nbsp;Yohei Sawada ,&nbsp;Riku Mitsui ,&nbsp;Toshiki Tsuboi ,&nbsp;Hirohiko Morimoto ,&nbsp;Junichi Fukushima ,&nbsp;Satoru Hayashi","doi":"10.1016/j.eucr.2026.103363","DOIUrl":"10.1016/j.eucr.2026.103363","url":null,"abstract":"<div><div>We report a rare case of bladder paraganglioma with lymph node metastasis. A 51-year-old man presented with gross hematuria caused by a bladder tumor. During transurethral resection, a sudden hypertensive crisis occurred, raising suspicion of a catecholamine-producing tumor. Pathological analysis confirmed bladder paraganglioma. Partial cystectomy combined with left pelvic lymph node dissection was performed because preoperative computed tomography showed mild swelling of the left obturator lymph node. At the time of writing, the patient has remained disease-free for 5 years. This case suggests that complete surgical resection may achieve long-term recurrence-free survival even in patients with localized lymph node metastasis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103363"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146188677","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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