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Metastatic gastric adenocarcinoma in prostate: A case report
IF 0.5
Urology Case Reports Pub Date : 2025-02-03 DOI: 10.1016/j.eucr.2025.102977
Naru Shimizu, Bunya Kawamoto, Kuniyasu Muraoka
{"title":"Metastatic gastric adenocarcinoma in prostate: A case report","authors":"Naru Shimizu,&nbsp;Bunya Kawamoto,&nbsp;Kuniyasu Muraoka","doi":"10.1016/j.eucr.2025.102977","DOIUrl":"10.1016/j.eucr.2025.102977","url":null,"abstract":"<div><div>We report a case of prostate cancer metastasis from gastric cancer. Prostate metastasis of gastric cancer as the primary tumor is very rare, and it is difficult to distinguish using hematoxylin and eosin (HE) staining alone. Because immunohistochemistry is also necessary, it is important to accurately share patient information with pathologists.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102977"},"PeriodicalIF":0.5,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143373079","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
Sarcomatoid renal pelvis carcinoma: A case report
IF 0.5
Urology Case Reports Pub Date : 2025-02-03 DOI: 10.1016/j.eucr.2025.102975
Xuechao Zhang , Yanan Jin , Weiran Zhang , Yawei Zhang , Haifeng Wang
{"title":"Sarcomatoid renal pelvis carcinoma: A case report","authors":"Xuechao Zhang ,&nbsp;Yanan Jin ,&nbsp;Weiran Zhang ,&nbsp;Yawei Zhang ,&nbsp;Haifeng Wang","doi":"10.1016/j.eucr.2025.102975","DOIUrl":"10.1016/j.eucr.2025.102975","url":null,"abstract":"<div><div>Sarcomatoid carcinoma is a malignant tumor of epithelial origin, some of the cells of which are differentiated in a sarcomatoid direction and are highly invasive. Sarcomatoid renal pelvis carcinoma (SRPC) is very rare. This article reports on an elderly woman with SRPC and discusses the clinical and pathological features and prognosis of SRPC in the hope of providing a reference for the diagnosis and treatment of this disease.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102975"},"PeriodicalIF":0.5,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143325120","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
Massive tubular ectasia of the rete testes in a patient with Marfan syndrome
IF 0.5
Urology Case Reports Pub Date : 2025-02-03 DOI: 10.1016/j.eucr.2025.102972
Ashley Lee , Su-Tong Low , Steve McCombie , Dickon Hayne
{"title":"Massive tubular ectasia of the rete testes in a patient with Marfan syndrome","authors":"Ashley Lee ,&nbsp;Su-Tong Low ,&nbsp;Steve McCombie ,&nbsp;Dickon Hayne","doi":"10.1016/j.eucr.2025.102972","DOIUrl":"10.1016/j.eucr.2025.102972","url":null,"abstract":"<div><div>This case study explores massive tubular ectasia of the rete testes in a patient with Marfan syndrome. Marfan syndrome is a connective tissue disorder and has no known association with tubular ectasia in published research. Despite the unclear pathophysiology of tubular ectasia, potential causes include mechanical obstruction and congenital deformity. The patient, a male in his 40s, presented with bilateral testicular pain and swelling up to a volume of 200 cc over two years. Tubular ectasia was diagnosed on ultrasound and MRI, no obstructive aetiology was identified. Initial conservative management was chosen, but further enlargement led to reconsideration of treatment options.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102972"},"PeriodicalIF":0.5,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143349760","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
Massive ureterocele leading to urinary retention in a male neonate: A rare presentation and successful management
IF 0.5
Urology Case Reports Pub Date : 2025-01-31 DOI: 10.1016/j.eucr.2025.102968
Rafael Nascimento Vilares, Manuela Horta, Afonso da Silva Alves Bento, Francisco Tibor Dénes, Roberto Iglesias Lopes
{"title":"Massive ureterocele leading to urinary retention in a male neonate: A rare presentation and successful management","authors":"Rafael Nascimento Vilares,&nbsp;Manuela Horta,&nbsp;Afonso da Silva Alves Bento,&nbsp;Francisco Tibor Dénes,&nbsp;Roberto Iglesias Lopes","doi":"10.1016/j.eucr.2025.102968","DOIUrl":"10.1016/j.eucr.2025.102968","url":null,"abstract":"<div><div>Ureterocele is a rare congenital anomaly characterized by the dilation of the distal ureter and its protrusion into the bladder, often related with duplex collecting renal system, leading to urinary obstruction.</div><div>While it commonly occurs in females, this case report presents the rare presentation of a massive ureterocele in a 2-day-old male neonate, causing urinary retention. A diagnostic workup revealed bilateral hydronephrosis and a massive ureterocele. Surgical intervention with endoscopic decompression of the ureterocele successfully alleviated the obstruction.</div><div>At one year follow-up, patient was completely asymptomatic and serial follow-up ultrasonography demonstrated resolution of hydronephrosis, highlighting the successful management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102968"},"PeriodicalIF":0.5,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138599","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
Renal immature teratoma in infant: A rare case report
IF 0.5
Urology Case Reports Pub Date : 2025-01-30 DOI: 10.1016/j.eucr.2025.102967
Yacobda Hamonangan Sigumonrong , Aze Andrea Putra
{"title":"Renal immature teratoma in infant: A rare case report","authors":"Yacobda Hamonangan Sigumonrong ,&nbsp;Aze Andrea Putra","doi":"10.1016/j.eucr.2025.102967","DOIUrl":"10.1016/j.eucr.2025.102967","url":null,"abstract":"<div><div>Renal teratoma is a rare malignant tumour originating from pluripotent cells. A five-month-old female presented with a painless abdominal mass initially suspected to be a Wilms tumor. A CT scan showed a large tumor in the left abdomen, leading to a left open nephrectomy. Histopathology confirmed an immature Grade III teratoma, showing ectodermal, mesodermal, and endodermal components with neuroepithelial structures. Post-operatively, the patient was stable with a good surgical wound. Diagnosis of renal teratoma relies on histology, as pre-operative imaging may mimic other tumors. Surgical removal is the primary treatment, with chemotherapy for recurrence if necessary.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102967"},"PeriodicalIF":0.5,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138194","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
Case report: Testicular manifestation of ANCA vasculitis
IF 0.5
Urology Case Reports Pub Date : 2025-01-30 DOI: 10.1016/j.eucr.2025.102966
Noah J. Sandel, Henry Wielzen
{"title":"Case report: Testicular manifestation of ANCA vasculitis","authors":"Noah J. Sandel,&nbsp;Henry Wielzen","doi":"10.1016/j.eucr.2025.102966","DOIUrl":"10.1016/j.eucr.2025.102966","url":null,"abstract":"<div><div>ANCA-associated vasculitis is a rare autoimmune disorder affecting small to medium-sized vessels, often targeting the respiratory tract and kidneys. Testicular involvement is rare and can resemble malignancy, leading to unnecessary surgery. A 36-year-old male presented with painful fingers, oral and nasal ulcers, and knee arthritis. Elevated proteinase 3 (PR3) antibodies confirmed PR3 ANCA-associated vasculitis. During hospitalization, patient developed testicular pain, and an ultrasound raised suspicion of malignancy. An inguinal orchidectomy was performed, revealing inflammation consistent with vasculitis, but no malignancy. Testicular involvement in ANCA vasculitis can mimic cancer, and increased awareness may help prevent unnecessary surgical procedures.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102966"},"PeriodicalIF":0.5,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138609","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
Bilateral testicular mass in a 21-year-old male with a history of congenital adrenal hyperplasia: A case report
IF 0.5
Urology Case Reports Pub Date : 2025-01-29 DOI: 10.1016/j.eucr.2025.102964
Amir Reza Abedi , Azade Rakhshan , Mohammad Seifi Poor
{"title":"Bilateral testicular mass in a 21-year-old male with a history of congenital adrenal hyperplasia: A case report","authors":"Amir Reza Abedi ,&nbsp;Azade Rakhshan ,&nbsp;Mohammad Seifi Poor","doi":"10.1016/j.eucr.2025.102964","DOIUrl":"10.1016/j.eucr.2025.102964","url":null,"abstract":"<div><div>A 21-year-old man was referred because of bilateral testicular swelling from 8 months ago. He had a known history of congenital adrenal hyperplasia (21-hydroxylase deficiency) diagnosed in infancy, managed with glucocorticoid therapy since childhood. However, the patient had been non-adherent to medication for several years. The patient underwent surgery with an inguinal incision, and a biopsy from the mass was sent for frozen section. The frozen and permanent sections were consistent with “Testicular adrenal rest tumor (tumor of adrenogenital syndrome)</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102964"},"PeriodicalIF":0.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138604","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
Tubulocystic renal cell carcinoma: Case report and literature review
IF 0.5
Urology Case Reports Pub Date : 2025-01-29 DOI: 10.1016/j.eucr.2025.102965
Yun-Shen Ding, Yi-Han Wang, Feng Liu
{"title":"Tubulocystic renal cell carcinoma: Case report and literature review","authors":"Yun-Shen Ding,&nbsp;Yi-Han Wang,&nbsp;Feng Liu","doi":"10.1016/j.eucr.2025.102965","DOIUrl":"10.1016/j.eucr.2025.102965","url":null,"abstract":"<div><div>To optimize the diagnosis and treatment of Tubulocystic renal cell carcinoma, we present our experience with a case of it and review the literature. Tubulocystic renal cell carcinoma (TRCC) is a rare subtype of renal carcinoma with distinctive histological and molecular characteristics. This study provides a comprehensive analysis of TRCC, focusing on its pathological features, diagnostic criteria, and potential molecular mechanisms. The findings highlight the unique histological architecture and biological behavior of TRCC, distinguishing it from other renal cell carcinomas. Advanced imaging techniques and molecular biomarkers play a pivotal role in its accurate diagnosis.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"59 ","pages":"Article 102965"},"PeriodicalIF":0.5,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143349759","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
Inflammatory myofibroblastic tumor of the right renal pelvis: A case report
IF 0.5
Urology Case Reports Pub Date : 2025-01-29 DOI: 10.1016/j.eucr.2025.102969
Xiaorui Zhu, Xueli Dong, Hongzhou Sheng, Renbin Deng, Xianzhong Duan
{"title":"Inflammatory myofibroblastic tumor of the right renal pelvis: A case report","authors":"Xiaorui Zhu,&nbsp;Xueli Dong,&nbsp;Hongzhou Sheng,&nbsp;Renbin Deng,&nbsp;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}
引用次数: 0
Rare presentation of urachal remnant with suprapubic sinus: A case report
IF 0.5
Urology Case Reports Pub Date : 2025-01-29 DOI: 10.1016/j.eucr.2025.102962
Sarah Cairo, Gabriella Grisotti, Hanmin Lee
{"title":"Rare presentation of urachal remnant with suprapubic sinus: A case report","authors":"Sarah Cairo,&nbsp;Gabriella Grisotti,&nbsp;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}
引用次数: 0
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