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Urology Case Reports最新文献

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Malignant pheochromocytoma invading the ureteral wall muscle layer: A case report 侵犯输尿管壁肌层的恶性嗜铬细胞瘤：病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-09-03 DOI: 10.1016/j.eucr.2024.102842
{"title":"Malignant pheochromocytoma invading the ureteral wall muscle layer: A case report","authors":"","doi":"10.1016/j.eucr.2024.102842","DOIUrl":"10.1016/j.eucr.2024.102842","url":null,"abstract":"<div><p>Pheochromocytoma is a neuroendocrine tumor for which surgical resection is the main treatment.Malignant pheochromocytoma is very rare. Here,we present a case of adrenal pheochromocytoma invading the ureteral wall muscle layer, which resulted in left adrenal and left nephrectomy.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001967/pdfft?md5=0253ae7e01b23ab1dcdd400f2ee8e27c&pid=1-s2.0-S2214442024001967-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142238382","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
Transrectal bladder prolapse in a male managed with a robotic-assisted laparoscopic cystoprostosacropexy 一名男性经直肠膀胱脱垂患者的机器人辅助腹腔镜膀胱前列腺切除术治疗方案
IF 0.5
Urology Case Reports Pub Date : 2024-09-03 DOI: 10.1016/j.eucr.2024.102834
{"title":"Transrectal bladder prolapse in a male managed with a robotic-assisted laparoscopic cystoprostosacropexy","authors":"","doi":"10.1016/j.eucr.2024.102834","DOIUrl":"10.1016/j.eucr.2024.102834","url":null,"abstract":"<div><p>Pelvic floor disorders frequently occur as the result of excessive straining from chronic constipation or the trauma of vaginal childbirth, making them more common in women. We present a 62-year-old male with bladder prolapse through the anterior rectal wall in the setting of longstanding bladder holding behavior and excessive straining to void. We performed a novel robotic-assisted laparoscopic cystoprostosacropexy by anchoring the bladder and prostate to the sacrum to prevent bladder descent. Postoperatively, the bladder prolapse resolved with return of normal urinary function. This case underscores the potential of innovative surgical techniques in managing complex pelvic floor disorders in males.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001888/pdfft?md5=2c9ca3add13fa439e2b78855f2f63c10&pid=1-s2.0-S2214442024001888-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142167494","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
Multicystic dysplastic kidney in adults: A case report of unilateral presentation in an adult sudanese female 成人多囊性发育不良肾脏：苏丹成年女性单侧发病的病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-09-02 DOI: 10.1016/j.eucr.2024.102839
{"title":"Multicystic dysplastic kidney in adults: A case report of unilateral presentation in an adult sudanese female","authors":"","doi":"10.1016/j.eucr.2024.102839","DOIUrl":"10.1016/j.eucr.2024.102839","url":null,"abstract":"<div><p>Multicystic dysplastic kidney is a congenital anomaly typically diagnosed in infancy, rare in adults, in our case of a 25-year-old Sudanese female presented with left flank pain. Imaging showed the left kidney replaced by cysts, consistent with MCDK, and ovarian cyst. She underwent a successful open simple nephrectomy; and histopathology confirmed MCDK. Our case highlights diagnostic and management challenges of MCDK in adults. Conservative management is increasing, especially for asymptomatic patients with normal contralateral kidney function. Healthcare barriers in Sudan, including limited awareness and political unrest, complicate timely diagnosis and treatment. Multidisciplinary care and improved healthcare access are essential.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001931/pdfft?md5=af7b4fdf5b24b36e27daf7d1cfe16875&pid=1-s2.0-S2214442024001931-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142164017","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
A rare case of renal leiomyosarcoma treated with partial nephrectomy 通过肾部分切除术治疗肾脏良性肉瘤的罕见病例
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102835
{"title":"A rare case of renal leiomyosarcoma treated with partial nephrectomy","authors":"","doi":"10.1016/j.eucr.2024.102835","DOIUrl":"10.1016/j.eucr.2024.102835","url":null,"abstract":"<div><p>Renal Leiomyosarcoma (LMS) is an exceptionally rare and aggressive form of RCC (renal cell carcinoma), comprising of 0.5–1% of all adult RCC. This disease constitutes a 5-year 25 % overall survival. We present a rare case of renal leiomyosarcoma in a 58 year-old Caucasian female with final pathologic staging of pT2 who underwent robotic-assisted right partial nephrectomy. Despite negative margins, given her aggressive histology, adjunctive treatment is discussed.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221444202400189X/pdfft?md5=739940a02d75aea3c6b84a46e797d00a&pid=1-s2.0-S221444202400189X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097976","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
Corrigendum to “Primary testicular teratoid Wilms tumor in a 40-year-old male with retroperitoneal lymph node involvement: A case report” [Urol Case Rep (March 2024) 102701] 40 岁男性原发性睾丸畸形 Wilms 肿瘤伴腹膜后淋巴结受累：病例报告" [Urol Case Rep (March 2024) 102701] 的更正
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102832
{"title":"Corrigendum to “Primary testicular teratoid Wilms tumor in a 40-year-old male with retroperitoneal lymph node involvement: A case report” [Urol Case Rep (March 2024) 102701]","authors":"","doi":"10.1016/j.eucr.2024.102832","DOIUrl":"10.1016/j.eucr.2024.102832","url":null,"abstract":"","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001864/pdfft?md5=adfd2b1fdc63e19b3a13dc72af11ed48&pid=1-s2.0-S2214442024001864-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142094847","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
Urachal inflammatory myofibroblastic tumor with FN1::ALK fusion: A case report and literature review 伴有FN1::ALK融合的尿道炎性肌纤维母细胞瘤：病例报告和文献综述
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102844
{"title":"Urachal inflammatory myofibroblastic tumor with FN1::ALK fusion: A case report and literature review","authors":"","doi":"10.1016/j.eucr.2024.102844","DOIUrl":"10.1016/j.eucr.2024.102844","url":null,"abstract":"<div><p>Urachal tumors are rare and comprise of both benign and malignant neoplasms. Epithelial origin tumors are more common than mesenchymal origin tumors. We report a case Urachal inflammatory myofibroblastic tumor (IMFT) in a 12 year old boy who presented with symptoms of lower abdominal pain and burning micturition. Upon evaluation was found to have a soft tissue mass anterior to urinary bladder wall. A laparoscopic excision of tumor was done. Histopathological and immunohistochemical examination confirmed the diagnosis of IMFT. Next generation sequencing identified FN1-ALK gene fusion.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001980/pdfft?md5=c80c9e623fd94672cb45c2986b039713&pid=1-s2.0-S2214442024001980-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097978","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
Chronic testicular pain after routine hydrocelectomy cured with epidural injection 硬膜外注射治愈常规鞘膜积液切除术后的慢性睾丸疼痛
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102829
{"title":"Chronic testicular pain after routine hydrocelectomy cured with epidural injection","authors":"","doi":"10.1016/j.eucr.2024.102829","DOIUrl":"10.1016/j.eucr.2024.102829","url":null,"abstract":"","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001839/pdfft?md5=d1a5ed576795b580c8422ec9bb618be7&pid=1-s2.0-S2214442024001839-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097977","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
Ovarian vein syndrome – Rare ovarian vein compression of the ureter 卵巢静脉综合征--罕见的卵巢静脉压迫输尿管
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102836
{"title":"Ovarian vein syndrome – Rare ovarian vein compression of the ureter","authors":"","doi":"10.1016/j.eucr.2024.102836","DOIUrl":"10.1016/j.eucr.2024.102836","url":null,"abstract":"<div><p>Ovarian vein syndrome is a rare condition involving the compression of the ureter by the ovarian vein. Since it was first described, very few cases have been reported in literature. We present a case of a 37-year-old female with typical symptoms and common right-side involvement. The imaging findings on ultrasound, CT, and nuclear medicine imaging are classic for her condition.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001906/pdfft?md5=f99eb560615b5c26fb712397f7f43ae5&pid=1-s2.0-S2214442024001906-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097979","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
Incidental testicular germ cell tumor in a transgender woman: A case report 变性女性偶发睾丸生殖细胞瘤：病例报告
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102817
{"title":"Incidental testicular germ cell tumor in a transgender woman: A case report","authors":"","doi":"10.1016/j.eucr.2024.102817","DOIUrl":"10.1016/j.eucr.2024.102817","url":null,"abstract":"<div><p>Testicular cancer found incidentally during gender-affirming orchiectomy is infrequently reported in the literature. This report details a 27-year-old transgender woman whose testicular cancer was discovered incidentally upon routine histopathologic examination of the orchiectomy specimen. The patient did not present with any clinical signs of malignancy. There was no evidence of metastases after further workup and the patient was able to resume hormone therapy after surgery. Transgender individuals must be screened according to their natal anatomy and even in absence of clinical signs excised tissue should be examined for possible malignancy.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214442024001712/pdfft?md5=b5ad14e7e7fbf749feed9c1d20b6ab22&pid=1-s2.0-S2214442024001712-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097975","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
Meatotomy and meatoplasty on meatal stenosis due to balanitis xerotica obliterans 肉腔切开术和肉腔成形术治疗毛囊炎引起的肉腔狭窄
IF 0.5
Urology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.eucr.2024.102838
{"title":"Meatotomy and meatoplasty on meatal stenosis due to balanitis xerotica obliterans","authors":"","doi":"10.1016/j.eucr.2024.102838","DOIUrl":"10.1016/j.eucr.2024.102838","url":null,"abstract":"<div><p>Balanitis xerotica obliterans (BXO) is a chronic inflammatory disease affecting the male genitalia that is mostly underdiagnosed and undertreatment. We presented a 40-year-old man with meatal stenosis and an inability to urinate. Discoloration at the tip of the penis was found, and he said it got wider as he grew up. We conducted meatotomy and meatoplasty to release obstruction. Early diagnosis is essential to avoid complications.</p></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221444202400192X/pdfft?md5=3aa310802127c2233faf1553a20b1e75&pid=1-s2.0-S221444202400192X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097973","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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