发布求助
文献互助 智能选刊 最新文献

Urology Case Reports最新文献

筛选
英文 中文
A rare giant renal angiomyolipoma in a 17-year-old male: A case report 一名 17 岁男性的罕见巨型肾血管瘤：病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-11-22 DOI: 10.1016/j.eucr.2024.102887
Fred Laizer , Hanson Nkini , Heri Babu , Erasto Medard , Amon Bamanyis , Teodros Veronesi
{"title":"A rare giant renal angiomyolipoma in a 17-year-old male: A case report","authors":"Fred Laizer ,&nbsp;Hanson Nkini ,&nbsp;Heri Babu ,&nbsp;Erasto Medard ,&nbsp;Amon Bamanyis ,&nbsp;Teodros Veronesi","doi":"10.1016/j.eucr.2024.102887","DOIUrl":"10.1016/j.eucr.2024.102887","url":null,"abstract":"<div><div>Renal angiomyolipoma is an uncommon benign tumor that mostly affects adults and is highly associated with tuberous sclerosis. It's very uncommon for it to affect adolescents. In this case, a 17-year-old male with abdominal pain and distension was diagnosed with sporadic giant renal angiomyolipoma. Histopathology confirmed the diagnosis after a successful nephrectomy. Though rare in teenagers, giant renal angiomyolipoma can be managed with surgery. Histopathology is a mainstay of confirming the diagnosis.</div></div><div><h3>Conclusion</h3><div>This case highlights the difficulties in managing big retroperitoneal tumors in teenagers and the necessity of taking sporadic angiomyolipoma into account when making a differential diagnosis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102887"},"PeriodicalIF":0.5,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142723873","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}
引用次数: 0
Comprehensive genomic profiling of primary bladder mucinous adenocarcinoma, a rare genitourinary cancer: A case report 原发性膀胱粘液腺癌--一种罕见的泌尿生殖系统癌症--的综合基因组图谱分析：病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-11-22 DOI: 10.1016/j.eucr.2024.102892
Shinkuro Yamamoto , Shingo Ashida , Tomoya Nao , Kaho Murakami , Ryohei Iga , Tsutomu Shimamoto , Hideo Fukuhara , Nobutaka Shimizu , Satoshi Fukata , Atsushi Kurabayashi , Takashi Karashima , Keiji Inoue
{"title":"Comprehensive genomic profiling of primary bladder mucinous adenocarcinoma, a rare genitourinary cancer: A case report","authors":"Shinkuro Yamamoto ,&nbsp;Shingo Ashida ,&nbsp;Tomoya Nao ,&nbsp;Kaho Murakami ,&nbsp;Ryohei Iga ,&nbsp;Tsutomu Shimamoto ,&nbsp;Hideo Fukuhara ,&nbsp;Nobutaka Shimizu ,&nbsp;Satoshi Fukata ,&nbsp;Atsushi Kurabayashi ,&nbsp;Takashi Karashima ,&nbsp;Keiji Inoue","doi":"10.1016/j.eucr.2024.102892","DOIUrl":"10.1016/j.eucr.2024.102892","url":null,"abstract":"<div><div>Primary bladder mucinous adenocarcinoma is a rare genitourinary cancer. Here, we present the case of a 75-year-old woman where pathological and imaging findings led to the diagnosis of primary bladder mucinous adenocarcinoma. She underwent treatment with paclitaxel–ifosfamide–cisplatin (TIP). After two cycles of TIP therapy, FoundationOne CDx, a comprehensive genomic profiling test, was performed, revealing variants in <em>ATM</em>, <em>SMAD4</em>, <em>BRD4</em>, and <em>NOTCH3</em>. These genomic profiling test results may lead to the development of novel therapeutic agents for primary bladder mucinous adenocarcinoma.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102892"},"PeriodicalIF":0.5,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142702425","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}
引用次数: 0
Atypical carcinoid of the primary kidney with retroperitoneal metastasis 15 years later: A case report and literature review 原发性肾脏非典型类癌，15 年后腹膜后转移：病例报告和文献综述
IF 0.5
Urology Case Reports Pub Date : 2024-11-21 DOI: 10.1016/j.eucr.2024.102893
Qiang Wang, Dong Zhuo, Houbao Huang, Jianping Tao
{"title":"Atypical carcinoid of the primary kidney with retroperitoneal metastasis 15 years later: A case report and literature review","authors":"Qiang Wang,&nbsp;Dong Zhuo,&nbsp;Houbao Huang,&nbsp;Jianping Tao","doi":"10.1016/j.eucr.2024.102893","DOIUrl":"10.1016/j.eucr.2024.102893","url":null,"abstract":"<div><div>Primary renal neuroendocrine tumors (NETs) are extremely rare among renal malignancies. According to pathological manifestations, carcinoid can be divided into four types: typical carcinoid, atypical carcinoid, large cell and small cell neuroendocrine carcinoma. Primary or secondary retroperitoneal carcinoid is even rarer than renal carcinoid. This article reports a patient with renal carcinoid complicated with retroperitoneal metastasis, who developed retroperitoneal metastasis 15 years after radical nephrectomy. Through the analysis of this case and the combination of the existing published literature, it is aimed to provide valuable references for clinicians in treating patients with renal carcinoid or with metastasis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102893"},"PeriodicalIF":0.5,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142702406","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}
引用次数: 0
Asymptomatic migration of ureteral stent to superior vena cava after ultrasound-guided percutaneous nephrolithotomy: An extremely rare case and review of the literature 超声引导下经皮肾镜碎石术后输尿管支架无症状移位至上腔静脉：极罕见病例及文献综述
IF 0.5
Urology Case Reports Pub Date : 2024-11-21 DOI: 10.1016/j.eucr.2024.102891
Amir Hossein Hassani , Hooman Kamran , Javad Kojuri , Helia Bazroodi , Hossein Fatemian , Alireza Rasekhi , Nima Naderi , Saeed Kooshafar , Anahita Dehghani , Abdolreza Haghpanah
{"title":"Asymptomatic migration of ureteral stent to superior vena cava after ultrasound-guided percutaneous nephrolithotomy: An extremely rare case and review of the literature","authors":"Amir Hossein Hassani ,&nbsp;Hooman Kamran ,&nbsp;Javad Kojuri ,&nbsp;Helia Bazroodi ,&nbsp;Hossein Fatemian ,&nbsp;Alireza Rasekhi ,&nbsp;Nima Naderi ,&nbsp;Saeed Kooshafar ,&nbsp;Anahita Dehghani ,&nbsp;Abdolreza Haghpanah","doi":"10.1016/j.eucr.2024.102891","DOIUrl":"10.1016/j.eucr.2024.102891","url":null,"abstract":"<div><div>Ureteral stent migration should be considered a rare complication of urologic procedures. We report a 69-year-old woman diagnosed with ureteral stent migration two weeks after undergoing percutaneous nephrolithotomy while she was symptom-free. The stent passed through the heart and extended to the superior vena cava and right brachiocephalic vein. After excluding thrombus formation, the stent was retrieved using an endovascular approach. Stent migration to the superior vena cava while being asymptomatic is extremely rare. Considering this complication is crucial to prevent consequent fatal events. This case report highlights this rare complication of ureteral stent placement and reviews its management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102891"},"PeriodicalIF":0.5,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142723871","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}
引用次数: 0
Imaging in Zinner Syndrome, A Case Series: The Wolf in Sheep’s Clothing 津纳综合征的成像，病例系列：披着羊皮的狼
IF 0.5
Urology Case Reports Pub Date : 2024-11-15 DOI: 10.1016/j.eucr.2024.102889
V. Pramod, S.C. Sanjay, S. Tanuj Sai Kumar
{"title":"Imaging in Zinner Syndrome, A Case Series: The Wolf in Sheep’s Clothing","authors":"V. Pramod,&nbsp;S.C. Sanjay,&nbsp;S. Tanuj Sai Kumar","doi":"10.1016/j.eucr.2024.102889","DOIUrl":"10.1016/j.eucr.2024.102889","url":null,"abstract":"<div><div>Zinner syndrome is a rare congenital malformation of the Wolffian duct with seminal vesicle cyst, ipsilateral renal agenesis and ejaculatory duct obstruction, seen in less than 0.002 % of the male population. An increased awareness among clinicians, urologists, and radiologists is essential, as early diagnosis and management can impact fertility outcomes. This review aims to explain and illustrate Zinner syndrome through imaging case studies. Emphasis is made on considering Zinner syndrome in the differential diagnosis of young males with pelvic pain and renal agenesis, highlighting the importance of radiological evaluation for the management of this uncommon yet clinically significant condition.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102889"},"PeriodicalIF":0.5,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142723872","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}
引用次数: 0
Neonatal epididymo-orchitis caused by Salmonella: A case of successful non-surgical management 沙门氏菌引起的新生儿附睾睾丸炎：一例成功的非手术治疗
IF 0.5
Urology Case Reports Pub Date : 2024-11-15 DOI: 10.1016/j.eucr.2024.102886
Avaneesh Kunta , Samantha Gibson , Abhishek Seth , Kenneth A. Alexander , Adriana Cadilla , Pamela Ellsworth
{"title":"Neonatal epididymo-orchitis caused by Salmonella: A case of successful non-surgical management","authors":"Avaneesh Kunta ,&nbsp;Samantha Gibson ,&nbsp;Abhishek Seth ,&nbsp;Kenneth A. Alexander ,&nbsp;Adriana Cadilla ,&nbsp;Pamela Ellsworth","doi":"10.1016/j.eucr.2024.102886","DOIUrl":"10.1016/j.eucr.2024.102886","url":null,"abstract":"<div><div>Neonatal epididymo-orchitis (EO) is a rare condition, particularly when caused by S<em>almonella</em>, a pathogen typically associated with gastroenteritis. We present the case of a 15-day-old male who developed right-sided scrotal swelling and erythema. Scrotal ultrasound confirmed EO without signs of torsion or abscess. Further investigation revealed potential <em>Salmonella</em> exposure from feeding bottles, and stool PCR confirmed the diagnosis. The patient responded well to antibiotics, avoiding surgical intervention. This case highlights the rarity of <em>Salmonella</em> EO in neonates and the value of early imaging, thorough history-taking, and environmental exposure assessment in guiding conservative management and avoiding surgery.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102886"},"PeriodicalIF":0.5,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142702405","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}
引用次数: 0
Urethral clear cell adenocarcinoma in an adult female: A rare case report 一名成年女性的尿道透明细胞腺癌：罕见病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-11-13 DOI: 10.1016/j.eucr.2024.102882
Yacob Sheiferawe Seman , Michael Teklehaimanot Abera , Fadil Nuredin Abrar , Tesfaye Kebede Legesse , Mesfin Asefa Tola , Tsiyon Nigusie Alemu
{"title":"Urethral clear cell adenocarcinoma in an adult female: A rare case report","authors":"Yacob Sheiferawe Seman ,&nbsp;Michael Teklehaimanot Abera ,&nbsp;Fadil Nuredin Abrar ,&nbsp;Tesfaye Kebede Legesse ,&nbsp;Mesfin Asefa Tola ,&nbsp;Tsiyon Nigusie Alemu","doi":"10.1016/j.eucr.2024.102882","DOIUrl":"10.1016/j.eucr.2024.102882","url":null,"abstract":"<div><div>Clear cell adenocarcinoma of the urethra is an extremely rare malignancy with a poor outcome, mainly affecting females in old age. We present the case of a 42-year-old female patient who presented with progressively worsening lower urinary tract symptoms, leading to a cystoscopy-guided core needle biopsy diagnosis of clear cell adenocarcinoma of the urethra. We will mainly discuss the cross-sectional imaging and pathological aspects of the case.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"58 ","pages":"Article 102882"},"PeriodicalIF":0.5,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142702404","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}
引用次数: 0
Spontaneous regression of metastatic clear cell renal cell carcinoma: A report of a rare case and a review of the literature 转移性透明细胞肾细胞癌的自然消退：一例罕见病例的报告和文献综述
IF 0.5
Urology Case Reports Pub Date : 2024-11-01 DOI: 10.1016/j.eucr.2024.102868
Anoushka Mullasseril , Anh B. Lam , Alekhya Mitta , Daniel Morton , Andrew McIntosh , Sanjay Patel , Theresa Thai , Anand Annan , Adanma Ayanambakkam
{"title":"Spontaneous regression of metastatic clear cell renal cell carcinoma: A report of a rare case and a review of the literature","authors":"Anoushka Mullasseril ,&nbsp;Anh B. Lam ,&nbsp;Alekhya Mitta ,&nbsp;Daniel Morton ,&nbsp;Andrew McIntosh ,&nbsp;Sanjay Patel ,&nbsp;Theresa Thai ,&nbsp;Anand Annan ,&nbsp;Adanma Ayanambakkam","doi":"10.1016/j.eucr.2024.102868","DOIUrl":"10.1016/j.eucr.2024.102868","url":null,"abstract":"<div><div>Renal cell carcinoma (RCC) is the seventh most common cancer in the United States; clear cell RCC (ccRCC) is the most common subtype. We report a case of spontaneous regression of metastatic ccRCC and discuss possible underlying mechanisms informed by a literature review. While regression of metastatic RCC has been described following nephrectomy or treatment of the primary tumor, spontaneous regression is rare. Postulated underlying causes include tumor necrosis and immune-mediated responses. Of 29 identified cases of spontaneous regression, only ours occurred after only a biopsy. Better understanding of the pathophysiology of spontaneous regression in RCC will improve its management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"57 ","pages":"Article 102868"},"PeriodicalIF":0.5,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142586530","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}
引用次数: 0
Complicated case of bilateral emphysematous pyelonephritis and emphysematous cystitis successfully treated with transurethral drainage and ureteral stents 经尿道引流和输尿管支架成功治疗双侧气肿性肾盂肾炎和气肿性膀胱炎的复杂病例
IF 0.5
Urology Case Reports Pub Date : 2024-11-01 DOI: 10.1016/j.eucr.2024.102877
Yoshihiro Kawaguchi , Yoshikado Miyagawa , Shigehisa Mizuta , Kosuke Ueda , Kiyoaki Nishihara , Makoto Nakiri , Tsukasa Igawa
{"title":"Complicated case of bilateral emphysematous pyelonephritis and emphysematous cystitis successfully treated with transurethral drainage and ureteral stents","authors":"Yoshihiro Kawaguchi ,&nbsp;Yoshikado Miyagawa ,&nbsp;Shigehisa Mizuta ,&nbsp;Kosuke Ueda ,&nbsp;Kiyoaki Nishihara ,&nbsp;Makoto Nakiri ,&nbsp;Tsukasa Igawa","doi":"10.1016/j.eucr.2024.102877","DOIUrl":"10.1016/j.eucr.2024.102877","url":null,"abstract":"<div><div>Emphysematous pyelonephritis and emphysematous cystitis are intractable diseases. Eight cases of bilateral emphysematous pyelonephritis and emphysematous cystitis have been reported, but no treatment has been established. An 88-year-old female was admitted with traumatic subarachnoid hemorrhage, and on the fourth day of hospitalization, she developed fever and septic shock. A computed tomography scan revealed bilateral emphysematous pyelonephritis and emphysematous cystitis. The patient was treated with bilateral double-J stents and an indwelling urethral catheter. This is the first report of bilateral emphysematous pyelonephritis and emphysematous cystitis treated conservatively with drainage and an internal stent, which may be a treatment option.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"57 ","pages":"Article 102877"},"PeriodicalIF":0.5,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142586529","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}
引用次数: 0
Hydronephrosis secondary to isolated renal tuberculosis in an immunocompetent adolescent: “A case report” 一名免疫功能正常的青少年继发于孤立性肾结核的肾积水："病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-11-01 DOI: 10.1016/j.eucr.2024.102876
Zamari Noori, Mohammad Jawid Nazari
{"title":"Hydronephrosis secondary to isolated renal tuberculosis in an immunocompetent adolescent: “A case report”","authors":"Zamari Noori,&nbsp;Mohammad Jawid Nazari","doi":"10.1016/j.eucr.2024.102876","DOIUrl":"10.1016/j.eucr.2024.102876","url":null,"abstract":"<div><div>Isolated renal tuberculosis is a rare form of extrapulmonary TB, especially in immunocompetent individuals. This case report details the diagnosis and management of a 14-year-old male who presented with massive hydronephrosis of unknown cause. Initial investigations, including urine cultures, were inconclusive. However, percutaneous nephrostomy provided a key diagnostic opportunity. This case highlights the importance of considering TB in the differential diagnosis of patients with unexplained urinary tract abnormalities, even in immunocompetent patients.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"57 ","pages":"Article 102876"},"PeriodicalIF":0.5,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142592943","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}
引用次数: 0
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信