首页 > 最新文献

Case Reports in Urology最新文献

英文 中文
Plasmacytoid Urothelial Carcinoma of the Bladder That Manifests Disseminated Carcinomatosis of the Bone Marrow: A Case Report of Extremely Rapid Progression. 表现为弥散性骨髓癌的膀胱浆细胞样尿路上皮癌:1例进展极快的报告。
Pub Date : 2022-09-15 eCollection Date: 2022-01-01 DOI: 10.1155/2022/6082700
Nobuhiko Shimizu, Yoshinobu Moritoki, Nao Katsumi, Takahiro Yanase, Teruaki Sugino, Kazuhiro Kanemoto, Hidetoshi Akita, Takahiro Yasui

Plasmacytoid urothelial carcinoma (PUC) of the bladder is a rare variant of invasive urothelial carcinoma (UC) with aggressive behavior. Despite its prognosis being poorer than that of conventional UC, a median overall survival of approximately 2 years is ensured when it is treated with radical cystectomy (RC), and few patients die within a few months of RC. In this paper, we report the case of a patient with PUC who developed widespread bone metastasis only 6 weeks after RC, which resulted in death within 2 months postoperatively.

膀胱浆细胞样尿路上皮癌(PUC)是一种罕见的侵袭性尿路上皮癌(UC)。尽管其预后比传统UC差,但当采用根治性膀胱切除术(RC)治疗时,中位总生存期约为2年,并且很少有患者在RC后几个月内死亡。在本文中,我们报告了一例PUC患者在RC术后仅6周发生广泛的骨转移,并在术后2个月内死亡。
{"title":"Plasmacytoid Urothelial Carcinoma of the Bladder That Manifests Disseminated Carcinomatosis of the Bone Marrow: A Case Report of Extremely Rapid Progression.","authors":"Nobuhiko Shimizu,&nbsp;Yoshinobu Moritoki,&nbsp;Nao Katsumi,&nbsp;Takahiro Yanase,&nbsp;Teruaki Sugino,&nbsp;Kazuhiro Kanemoto,&nbsp;Hidetoshi Akita,&nbsp;Takahiro Yasui","doi":"10.1155/2022/6082700","DOIUrl":"https://doi.org/10.1155/2022/6082700","url":null,"abstract":"<p><p>Plasmacytoid urothelial carcinoma (PUC) of the bladder is a rare variant of invasive urothelial carcinoma (UC) with aggressive behavior. Despite its prognosis being poorer than that of conventional UC, a median overall survival of approximately 2 years is ensured when it is treated with radical cystectomy (RC), and few patients die within a few months of RC. In this paper, we report the case of a patient with PUC who developed widespread bone metastasis only 6 weeks after RC, which resulted in death within 2 months postoperatively.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"6082700"},"PeriodicalIF":0.0,"publicationDate":"2022-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499816/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33482434","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: 1
A Rare Case Report of Giant Urinary Bladder Stone Causing Recurrent Dysuria in a Woman. 1例罕见的女性巨大膀胱结石引起复发性排尿困难。
Pub Date : 2022-08-27 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4835945
Rojan Adhikari, Hari Prasad Baral, Utsav Bhattarai, Ravi Kiran Gautam, Kiran Jung Kunwar, Dipesh Shrestha, Bijay Mansingh Katwal

Background: Large urinary bladder stones are not common and even less common in females. We report a case of large bladder stone presented with acute retention of urine in a female patient. Case Report. A 62-year-old female presented in emergency department with retention of urine for 12 hours with history of recurrent UTIs for last 1 year. She was also complaining of mild dull lower abdominal pain for last 6 months. She had no history of incontinence of urine and fever. On physical examination, hard mass was palpable on suprapubic region on palpation of abdomen. Urine culture shows Escherichia coli for which antibiotics was given. An X-ray kidney ureter bladder showed a radio-opacity in the pelvic region measuring 9 × 8 cm in size. Ultrasonography revealed bilateral mild hydronephrosis with a large bladder stone. Open cystolithotomy was performed, and the stone was taken out. Stone biochemical analysis showed predominantly urate crystals. Patient had uneventful postoperative course, and she was discharged on 4th postoperative day and was followed up for 1 months after operation.

Conclusions: Large urinary bladder stones are not common and even less common in females. Clinician should have think regarding large bladder stone as a cause of recurrent lower urinary tract symptoms like dysuria and should assess renal function for proper treatment. Open cystolithotomy is choice of operation in large bladder stone.

背景:大膀胱结石在女性中并不常见,更不常见。我们报告一个病例大膀胱结石提出急性尿潴留在一个女性病人。病例报告。一名62岁女性因尿潴留12小时就诊于急诊科,既往有1年尿路感染复发史。她还主诉过去6个月有轻微的下腹钝痛。患者无尿失禁及发热病史。查体腹部触诊耻骨上可见硬块。尿液培养显示有大肠杆菌,使用了抗生素。肾输尿管膀胱x线片示9 × 8cm大小的骨盆区放射影。超声显示双侧轻度肾积水伴大膀胱结石。开腹取石术取出结石。石的生化分析显示主要为尿酸盐晶体。患者术后过程平稳,术后第4天出院,术后随访1个月。结论:大膀胱结石在女性中并不常见,更不常见。临床医生应考虑到大膀胱结石是反复出现的下尿路症状如排尿困难的原因,并应评估肾功能以进行适当的治疗。开放膀胱取石术是治疗大膀胱结石的首选手术方法。
{"title":"A Rare Case Report of Giant Urinary Bladder Stone Causing Recurrent Dysuria in a Woman.","authors":"Rojan Adhikari,&nbsp;Hari Prasad Baral,&nbsp;Utsav Bhattarai,&nbsp;Ravi Kiran Gautam,&nbsp;Kiran Jung Kunwar,&nbsp;Dipesh Shrestha,&nbsp;Bijay Mansingh Katwal","doi":"10.1155/2022/4835945","DOIUrl":"https://doi.org/10.1155/2022/4835945","url":null,"abstract":"<p><strong>Background: </strong>Large urinary bladder stones are not common and even less common in females. We report a case of large bladder stone presented with acute retention of urine in a female patient. <i>Case Report</i>. A 62-year-old female presented in emergency department with retention of urine for 12 hours with history of recurrent UTIs for last 1 year. She was also complaining of mild dull lower abdominal pain for last 6 months. She had no history of incontinence of urine and fever. On physical examination, hard mass was palpable on suprapubic region on palpation of abdomen. Urine culture shows Escherichia coli for which antibiotics was given. An X-ray kidney ureter bladder showed a radio-opacity in the pelvic region measuring 9 × 8 cm in size. Ultrasonography revealed bilateral mild hydronephrosis with a large bladder stone. Open cystolithotomy was performed, and the stone was taken out. Stone biochemical analysis showed predominantly urate crystals. Patient had uneventful postoperative course, and she was discharged on 4<sup>th</sup> postoperative day and was followed up for 1 months after operation.</p><p><strong>Conclusions: </strong>Large urinary bladder stones are not common and even less common in females. Clinician should have think regarding large bladder stone as a cause of recurrent lower urinary tract symptoms like dysuria and should assess renal function for proper treatment. Open cystolithotomy is choice of operation in large bladder stone.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"4835945"},"PeriodicalIF":0.0,"publicationDate":"2022-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440851/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40352283","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: 1
Male Perineal Carcinoma: Experience in 4 Cases and Literature Review. 男性会阴癌4例分析及文献复习。
Pub Date : 2022-08-22 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4466602
Agustín Fraile Poblador, Manuel Hevia Palacios, Manuel Rodríguez Vegas, Alberto Artiles Medina, Enrique Sanz Mayayo, Silvia García Barreras, Guillermo Fernández Conejo, Rafael Rodríguez Patrón, Varona Crespo Constatino, Ana Saiz González, Javier Burgos Revilla

Perineal carcinoma of unknown origin is a rare and aggressive disease, so an early diagnosis and adequate treatment are essential to prevent its progression. We report the first series of cases of perineal carcinoma of unknown origin: (I) a 62-year-old male patient being followed up for a urethral stricture treated with periodic dilations with subsequent development of perineal abscesses and perineal carcinoma; (II) a 67-year-old male patient who consults for urinary discomfort associated with a perineal abscess. Recurrence of the abscess in the first month revealed the presence of an underlying perineal carcinoma; (III) a 78-year-old male patient that underwent urethroplasty with graft with subsequent regimen of periodical dilations. Recurrent formation of perianal abscesses revealed the presence of an underlying perineal carcinoma; and (IV) a 78-year-old male patient with history of in situ penile carcinoma treated by glans resurfacing. He consulted for penile pain, and imaging tests revealed a perineal abscess adjacent to the left corpus cavernosum. The core needle biopsy revealed a squamous cell carcinoma. Penile exploration and negative glans biopsy ruled out possible recurrence of penile carcinoma. The form of presentation of the disease has been very similar in all patients, demonstrating the presence of perineal abscess in all cases. Two patients had inguinal lymph node disease at diagnosis. All patients were treated by surgery, and three of them required adjuvant systemic treatment. Surgery combined with systemic treatment is probably the best option if the patient's conditions allow it.

来历不明的会阴癌是一种罕见的侵袭性疾病,因此早期诊断和适当的治疗对于防止其发展至关重要。我们报告了一系列不明原因的会阴癌病例:(1)一名62岁男性患者因尿道狭窄接受周期性扩张治疗,随后发展为会阴脓肿和会阴癌;(II)一位67岁男性患者,因会阴脓肿引起尿路不适而就诊。第一个月的脓肿复发表明会阴癌的存在;(III)一位78岁男性患者接受了移植尿道成形术,随后进行了周期性扩张治疗。肛周脓肿复发提示会阴癌的存在;(IV) 78岁男性,既往有阴茎原位癌,经龟头置换治疗。他咨询了阴茎疼痛,影像学检查显示左侧海绵体附近有会阴脓肿。核心穿刺活检显示为鳞状细胞癌。阴茎探查和阴性的龟头活检排除了阴茎癌复发的可能。该疾病的表现形式在所有患者中都非常相似,在所有病例中都表现为会阴脓肿。2例患者诊断时有腹股沟淋巴结病变。所有患者均行手术治疗,其中3例需要辅助全身治疗。如果病人的情况允许,手术结合全身治疗可能是最好的选择。
{"title":"Male Perineal Carcinoma: Experience in 4 Cases and Literature Review.","authors":"Agustín Fraile Poblador,&nbsp;Manuel Hevia Palacios,&nbsp;Manuel Rodríguez Vegas,&nbsp;Alberto Artiles Medina,&nbsp;Enrique Sanz Mayayo,&nbsp;Silvia García Barreras,&nbsp;Guillermo Fernández Conejo,&nbsp;Rafael Rodríguez Patrón,&nbsp;Varona Crespo Constatino,&nbsp;Ana Saiz González,&nbsp;Javier Burgos Revilla","doi":"10.1155/2022/4466602","DOIUrl":"https://doi.org/10.1155/2022/4466602","url":null,"abstract":"<p><p>Perineal carcinoma of unknown origin is a rare and aggressive disease, so an early diagnosis and adequate treatment are essential to prevent its progression. We report the first series of cases of perineal carcinoma of unknown origin: (I) a 62-year-old male patient being followed up for a urethral stricture treated with periodic dilations with subsequent development of perineal abscesses and perineal carcinoma; (II) a 67-year-old male patient who consults for urinary discomfort associated with a perineal abscess. Recurrence of the abscess in the first month revealed the presence of an underlying perineal carcinoma; (III) a 78-year-old male patient that underwent urethroplasty with graft with subsequent regimen of periodical dilations. Recurrent formation of perianal abscesses revealed the presence of an underlying perineal carcinoma; and (IV) a 78-year-old male patient with history of in situ penile carcinoma treated by glans resurfacing. He consulted for penile pain, and imaging tests revealed a perineal abscess adjacent to the left corpus cavernosum. The core needle biopsy revealed a squamous cell carcinoma. Penile exploration and negative glans biopsy ruled out possible recurrence of penile carcinoma. The form of presentation of the disease has been very similar in all patients, demonstrating the presence of perineal abscess in all cases. Two patients had inguinal lymph node disease at diagnosis. All patients were treated by surgery, and three of them required adjuvant systemic treatment. Surgery combined with systemic treatment is probably the best option if the patient's conditions allow it.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"4466602"},"PeriodicalIF":0.0,"publicationDate":"2022-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424042/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40336015","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
Colon Cancer Metastasis to the Right Testis: Case Report and Review of Literature. 结肠癌转移至右睾丸:病例报告和文献综述。
Pub Date : 2022-08-18 eCollection Date: 2022-01-01 DOI: 10.1155/2022/2649259
Mizuki Kasahara, Tomo Shimizu, Hiroshi Aoki, Mizuho Okawa, Fumito Yamabe, Hideyuki Kobayashi, Koichi Nagao, Koichi Nakajima, Yozo Mitsui

Introduction: A metastatic testicular tumor is uncommon. We report here a case of testicular metastasis associated with recurrent colorectal cancer. Case Presentation. A 75-year-old male was presented with right scrotum pain one year after undergoing a right hemicolectomy combined with resection of the small intestine and omentum for ascending colon cancer (pT4N0M0). Magnetic resonance imaging of the pelvis showed a 7.3 × 5.4 × 4.5 cm mass consisting of a cystic solid tumor. A right inguinal orchiectomy was performed and right testicular pain improved after surgery. Pathology results showed that the tumor was a metastatic adenocarcinoma. The patient subsequently died two months later due to progression of the colon cancer.

Conclusion: Although colorectal cancer metastasis to the testis is very uncommon, it should be kept in mind in clinical situations, especially for older males with a testicular mass or discomfort.

简介转移性睾丸肿瘤并不常见。我们在此报告一例伴有复发性结肠直肠癌的睾丸转移病例。病例介绍。一名 75 岁的男性因患升结肠癌(pT4N0M0)接受右半结肠切除术和小肠及网膜切除术一年后出现右侧阴囊疼痛。骨盆磁共振成像显示,该患者有一个 7.3 × 5.4 × 4.5 厘米的囊性实体瘤肿块。患者接受了右侧腹股沟睾丸切除术,术后右侧睾丸疼痛有所改善。病理结果显示肿瘤为转移性腺癌。两个月后,患者因结肠癌恶化而死亡:虽然结肠癌转移到睾丸的情况非常少见,但在临床上,尤其是对有睾丸肿块或不适的老年男性来说,应牢记这一点。
{"title":"Colon Cancer Metastasis to the Right Testis: Case Report and Review of Literature.","authors":"Mizuki Kasahara, Tomo Shimizu, Hiroshi Aoki, Mizuho Okawa, Fumito Yamabe, Hideyuki Kobayashi, Koichi Nagao, Koichi Nakajima, Yozo Mitsui","doi":"10.1155/2022/2649259","DOIUrl":"10.1155/2022/2649259","url":null,"abstract":"<p><strong>Introduction: </strong>A metastatic testicular tumor is uncommon. We report here a case of testicular metastasis associated with recurrent colorectal cancer. <i>Case Presentation</i>. A 75-year-old male was presented with right scrotum pain one year after undergoing a right hemicolectomy combined with resection of the small intestine and omentum for ascending colon cancer (pT4N0M0). Magnetic resonance imaging of the pelvis showed a 7.3 × 5.4 × 4.5 cm mass consisting of a cystic solid tumor. A right inguinal orchiectomy was performed and right testicular pain improved after surgery. Pathology results showed that the tumor was a metastatic adenocarcinoma. The patient subsequently died two months later due to progression of the colon cancer.</p><p><strong>Conclusion: </strong>Although colorectal cancer metastasis to the testis is very uncommon, it should be kept in mind in clinical situations, especially for older males with a testicular mass or discomfort.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"2649259"},"PeriodicalIF":0.0,"publicationDate":"2022-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411008/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33444604","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
Penile Hair Tourniquet Syndrome (PHTS): A Case Report of a Two-Year-Old Boy. 阴茎毛发止血带综合征(PHTS): 1例2岁男童。
Pub Date : 2022-08-09 eCollection Date: 2022-01-01 DOI: 10.1155/2022/8030934
Alhareth Baarimah, Latif Dar, Rayan Dashnan, Saeed Alshahrani, Mohammed Beaiti, Khaled ALDhabaan

Penile hair tourniquet syndrome (PHTS) is an unusual phenomenon. A physician should have a high index of suspicion when a circumcised child presents with glans swelling and inflammation. It must be considered a surgical emergency, as early diagnosis and treatment can prevent complications (e.g., urethra-cutaneous fistula, complete urethral transection, penile gangrene, and penile amputation). We report a case of two-year-old boy to highlight the importance of early diagnosis and prompt treatment.

阴茎毛发止血带综合征(PHTS)是一种罕见的现象。当一个包皮环切的孩子出现龟头肿胀和炎症时,医生应该高度怀疑。必须将其视为外科急诊,因为早期诊断和治疗可以预防并发症(如尿道-皮瘘、尿道完全横断、阴茎坏疽和阴茎截肢)。我们报告一个两岁男孩的病例,以强调早期诊断和及时治疗的重要性。
{"title":"Penile Hair Tourniquet Syndrome (PHTS): A Case Report of a Two-Year-Old Boy.","authors":"Alhareth Baarimah,&nbsp;Latif Dar,&nbsp;Rayan Dashnan,&nbsp;Saeed Alshahrani,&nbsp;Mohammed Beaiti,&nbsp;Khaled ALDhabaan","doi":"10.1155/2022/8030934","DOIUrl":"https://doi.org/10.1155/2022/8030934","url":null,"abstract":"<p><p>Penile hair tourniquet syndrome (PHTS) is an unusual phenomenon. A physician should have a high index of suspicion when a circumcised child presents with glans swelling and inflammation. It must be considered a surgical emergency, as early diagnosis and treatment can prevent complications (e.g., urethra-cutaneous fistula, complete urethral transection, penile gangrene, and penile amputation). We report a case of two-year-old boy to highlight the importance of early diagnosis and prompt treatment.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"8030934"},"PeriodicalIF":0.0,"publicationDate":"2022-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381260/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40638673","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
Necrotizing Epididymo-Orchitis: A Rare Manifestation of COVID-19. 坏死性附睾-睾丸炎:COVID-19的一种罕见表现。
Pub Date : 2022-07-01 eCollection Date: 2022-01-01 DOI: 10.1155/2022/1891429
Ali Tavoosian, Sana Ahmadi, Seyed Mohammad Kazem Aghamir

Epididymo-orchitis is an infection of the epididymis and testis, one of the most common urogenital infections. It can be seen at any age. It is caused by sexually transmitted microorganisms and nonsexual transmitted pathogens. Viruses such as mumps and cytomegalovirus can also cause epididymo-orchitis. During the COVID-19 pandemic, in case of abnormal clinical manifestations of COVID infection and inadequate therapeutic response to the routine therapies, this disease with unusual manifestations should be considered. The case introduced in this paper is a 55-year-old man referred to a urology clinic with typical clinical presentations of epididymo-orchitis. Diagnosis by color Doppler examination and ultrasound also confirmed epididymo-orchitis. The patient underwent appropriate and routine treatment for epididymo-orchitis. Because of the lack of adequate clinical response and the continuation of fever and the development of scrotal lesions and the results of the control ultrasound, which suggested rupture of the tunica albuginea capsule, he underwent surgical exploration and subsequent orchiectomy. Due to the unconventional conditions and the usual culture and pathology, COVID-19 PCR was also performed on the tissues. The PCR showed tissue infection with COVID-19. The patient's clinical condition improved with an orchiectomy, the fever stopped, and he was discharged in a good general condition. It should be noted that before referral to the urology clinic and during hospitalization, evaluation, and treatment, the patient had no evidence in favor of respiratory tract infection with the coronavirus.

附睾-睾丸炎是一种附睾和睾丸的感染,是最常见的泌尿生殖道感染之一。它可以在任何年龄看到。它是由性传播微生物和非性传播病原体引起的。流行性腮腺炎和巨细胞病毒等病毒也可引起附睾睾丸炎。在新冠肺炎大流行期间,如发现新冠肺炎感染临床表现异常,常规治疗效果不佳,应考虑为表现异常的疾病。本文介绍的病例是一名55岁的男性,以典型的附睾睾丸炎的临床表现转介到泌尿科诊所。彩色多普勒检查和超声诊断也证实附睾睾丸炎。患者接受了适当和常规的治疗附睾睾丸炎。由于缺乏足够的临床反应,持续发烧和阴囊病变的发展,以及对照超声结果提示白膜囊破裂,他接受了手术探查和随后的睾丸切除术。由于非常规条件和常规的培养和病理,我们还对组织进行了COVID-19 PCR。PCR结果显示组织感染。患者行睾丸切除术后临床情况好转,发热停止,出院时一般情况良好。值得注意的是,在转诊泌尿科门诊前以及住院、评估和治疗期间,患者未发现呼吸道感染冠状病毒的证据。
{"title":"Necrotizing Epididymo-Orchitis: A Rare Manifestation of COVID-19.","authors":"Ali Tavoosian,&nbsp;Sana Ahmadi,&nbsp;Seyed Mohammad Kazem Aghamir","doi":"10.1155/2022/1891429","DOIUrl":"https://doi.org/10.1155/2022/1891429","url":null,"abstract":"<p><p>Epididymo-orchitis is an infection of the epididymis and testis, one of the most common urogenital infections. It can be seen at any age. It is caused by sexually transmitted microorganisms and nonsexual transmitted pathogens. Viruses such as mumps and cytomegalovirus can also cause epididymo-orchitis. During the COVID-19 pandemic, in case of abnormal clinical manifestations of COVID infection and inadequate therapeutic response to the routine therapies, this disease with unusual manifestations should be considered. The case introduced in this paper is a 55-year-old man referred to a urology clinic with typical clinical presentations of epididymo-orchitis. Diagnosis by color Doppler examination and ultrasound also confirmed epididymo-orchitis. The patient underwent appropriate and routine treatment for epididymo-orchitis. Because of the lack of adequate clinical response and the continuation of fever and the development of scrotal lesions and the results of the control ultrasound, which suggested rupture of the tunica albuginea capsule, he underwent surgical exploration and subsequent orchiectomy. Due to the unconventional conditions and the usual culture and pathology, COVID-19 PCR was also performed on the tissues. The PCR showed tissue infection with COVID-19. The patient's clinical condition improved with an orchiectomy, the fever stopped, and he was discharged in a good general condition. It should be noted that before referral to the urology clinic and during hospitalization, evaluation, and treatment, the patient had no evidence in favor of respiratory tract infection with the coronavirus.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"1891429"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250965/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40487301","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: 1
Primary Adenosquamous Carcinoma of the Prostate with Rectal Invasion. 原发性前列腺腺鳞癌伴直肠侵犯。
Pub Date : 2022-06-24 eCollection Date: 2022-01-01 DOI: 10.1155/2022/7613482
Pierre Azzi, Dominique Bossé, Ilias Cagiannos, Paul Borowy-Borowski, David Tiberi

Prostate adenosquamous carcinoma (pASC) is a rare form of prostate cancer accounting for <1% of all cases. It is generally considered an aggressive variant often presenting with significant symptom burden and/or metastatic disease. Given its rarity, optimal management of this cancer is unknown. We present a case of a patient with pASC treated with radiotherapy and chemotherapy with excellent symptomatic improvement and local control.

前列腺腺鳞癌(pASC)是一种罕见的前列腺癌
{"title":"Primary Adenosquamous Carcinoma of the Prostate with Rectal Invasion.","authors":"Pierre Azzi,&nbsp;Dominique Bossé,&nbsp;Ilias Cagiannos,&nbsp;Paul Borowy-Borowski,&nbsp;David Tiberi","doi":"10.1155/2022/7613482","DOIUrl":"https://doi.org/10.1155/2022/7613482","url":null,"abstract":"<p><p>Prostate adenosquamous carcinoma (pASC) is a rare form of prostate cancer accounting for <1% of all cases. It is generally considered an aggressive variant often presenting with significant symptom burden and/or metastatic disease. Given its rarity, optimal management of this cancer is unknown. We present a case of a patient with pASC treated with radiotherapy and chemotherapy with excellent symptomatic improvement and local control.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"7613482"},"PeriodicalIF":0.0,"publicationDate":"2022-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249496/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40556931","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: 1
Laparoscopic Nephroureterectomy with Heminephrectomy for Urothelial Carcinoma of the Upper Renal Pelvis on the Left Side of the Horseshoe Kidney. 腹腔镜肾输尿管切除术联合半肾切除术治疗马蹄肾左侧上肾盂尿路上皮癌。
Pub Date : 2022-06-21 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4985041
Taro Ikeda, Kazunori Matsumoto, Go Hasegawa, Yohei Ikeda, Noboru Hara, Tsutomu Nishiyama

A 70-year-old male was diagnosed with urothelial carcinoma of the upper renal pelvis on the left side of the horseshoe kidney. Preoperative thin-slice contrast-enhanced CT with three-dimensional reconstruction of the images revealed that two arteries arising from the aorta supplied the left moiety of the horseshoe kidney. He underwent laparoscopic transperitoneal nephroureterectomy with heminephrectomy on the left side of the horseshoe kidney visualized by indocyanine green fluorescence system. The histopathological findings of the renal pelvic tumor revealed invasive urothelial carcinoma with squamous differentiation, high grade, and pT3.

一位70岁男性被诊断为马蹄肾左侧上肾盂尿路上皮癌。术前薄层增强CT三维重建图像显示,两条源自主动脉的动脉供应左马蹄肾。他接受了腹腔镜经腹膜肾输尿管切除术和左马蹄肾半肾切除术,吲哚菁绿荧光系统显示。肾盆腔肿瘤病理表现为浸润性尿路上皮癌,呈鳞状分化,高分级,pT3。
{"title":"Laparoscopic Nephroureterectomy with Heminephrectomy for Urothelial Carcinoma of the Upper Renal Pelvis on the Left Side of the Horseshoe Kidney.","authors":"Taro Ikeda,&nbsp;Kazunori Matsumoto,&nbsp;Go Hasegawa,&nbsp;Yohei Ikeda,&nbsp;Noboru Hara,&nbsp;Tsutomu Nishiyama","doi":"10.1155/2022/4985041","DOIUrl":"https://doi.org/10.1155/2022/4985041","url":null,"abstract":"<p><p>A 70-year-old male was diagnosed with urothelial carcinoma of the upper renal pelvis on the left side of the horseshoe kidney. Preoperative thin-slice contrast-enhanced CT with three-dimensional reconstruction of the images revealed that two arteries arising from the aorta supplied the left moiety of the horseshoe kidney. He underwent laparoscopic transperitoneal nephroureterectomy with heminephrectomy on the left side of the horseshoe kidney visualized by indocyanine green fluorescence system. The histopathological findings of the renal pelvic tumor revealed invasive urothelial carcinoma with squamous differentiation, high grade, and pT3.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"4985041"},"PeriodicalIF":0.0,"publicationDate":"2022-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239762/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40462635","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: 1
Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma. 转移至膀胱:肾细胞癌复发的罕见部位。
Pub Date : 2022-06-17 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4339270
Amanda Smart, Michael Wynne, Ezra Baraban, Yasser Ged, Armine Smith

Renal cell carcinoma (RCC) is considered to be the deadliest urologic cancer with high rates of metastasis and recurrence after nephrectomy. RCC can metastasize to nearly any organ but most commonly metastasizes to the liver, lung, brain, and bone. To date, there are only about 40 reported cases of RCC with solitary bladder metastasis. The following report contributes to this limited data set of patients with RCC who develop solitary metastasis to the bladder. A 69-year-old male presented with occasional gross hematuria and was found to have a left renal mass infiltrating the collecting system. Ureteroscopic biopsy revealed clear cell RCC, and the patient subsequently underwent radical left nephrectomy. Eight months after nephrectomy, the patient presented to the clinic with gross hematuria. In-office cystoscopy demonstrated a nodular lesion in the bladder arising from the left ureteral orifice. The patient underwent transurethral resection of the bladder mass and pathology demonstrated clear cell RCC. Subsequent imaging showed no evidence of metastatic disease. Five months after transurethral resection, the patient was found to have a left distal ureteral mass and underwent left ureterectomy with partial cystectomy. Pathology again demonstrated clear cell RCC. RCC with solitary metastasis to the bladder is rare, and there are no targeted guideline recommendations for management. Per standard of care, patients with painless hematuria and risk factors for malignancy should undergo cystoscopy. In patients with a history of RCC, metastasis to the bladder should be considered in the differential diagnosis. Patients with metastatic RCC to the bladder should undergo a thorough work-up for additional sites of metastasis. In patients with RCC who develop solitary bladder metastasis amenable to resection following nephrectomy, there is a lack of evidence to guide therapy and a multidisciplinary discussion is warranted. However, if the tumor is amenable to resection, metastasectomy is a reasonable therapeutic approach and offers the patient an improved quality of life and an opportunity for remission.

肾细胞癌(RCC)被认为是最致命的泌尿系统癌症,肾切除术后的转移率和复发率都很高。RCC 几乎可以转移到任何器官,但最常见的是转移到肝、肺、脑和骨。迄今为止,仅有约 40 例 RCC 单发膀胱转移的报道。以下报告为这一有限的数据集做出了贡献:RCC 患者单发转移至膀胱。一名 69 岁的男性患者出现偶发性毛细血尿,发现左肾肿块浸润集合系统。输尿管镜活检显示患者为透明细胞 RCC,随后患者接受了左肾根治性切除术。肾切除术后八个月,患者因严重血尿就诊。诊室膀胱镜检查显示,膀胱内的结节性病变来自左侧输尿管口。患者接受了经尿道膀胱肿块切除术,病理结果显示为透明细胞型红斑狼疮。随后的影像学检查未发现转移性疾病。经尿道切除术五个月后,患者被发现左侧输尿管远端有肿块,于是接受了左侧输尿管切除术和部分膀胱切除术。病理再次显示为透明细胞 RCC。单发转移至膀胱的 RCC 比较罕见,目前还没有针对性的治疗指南建议。根据治疗标准,有无痛性血尿和恶性肿瘤危险因素的患者应接受膀胱镜检查。对于有 RCC 病史的患者,在鉴别诊断时应考虑膀胱转移。RCC转移至膀胱的患者应进行全面检查,以确定是否有其他转移部位。对于在肾切除术后出现可进行切除的单发膀胱转移瘤的 RCC 患者,目前缺乏指导治疗的证据,因此需要进行多学科讨论。不过,如果肿瘤可以切除,转移灶切除术是一种合理的治疗方法,可提高患者的生活质量,并为病情缓解提供机会。
{"title":"Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma.","authors":"Amanda Smart, Michael Wynne, Ezra Baraban, Yasser Ged, Armine Smith","doi":"10.1155/2022/4339270","DOIUrl":"10.1155/2022/4339270","url":null,"abstract":"<p><p>Renal cell carcinoma (RCC) is considered to be the deadliest urologic cancer with high rates of metastasis and recurrence after nephrectomy. RCC can metastasize to nearly any organ but most commonly metastasizes to the liver, lung, brain, and bone. To date, there are only about 40 reported cases of RCC with solitary bladder metastasis. The following report contributes to this limited data set of patients with RCC who develop solitary metastasis to the bladder. A 69-year-old male presented with occasional gross hematuria and was found to have a left renal mass infiltrating the collecting system. Ureteroscopic biopsy revealed clear cell RCC, and the patient subsequently underwent radical left nephrectomy. Eight months after nephrectomy, the patient presented to the clinic with gross hematuria. In-office cystoscopy demonstrated a nodular lesion in the bladder arising from the left ureteral orifice. The patient underwent transurethral resection of the bladder mass and pathology demonstrated clear cell RCC. Subsequent imaging showed no evidence of metastatic disease. Five months after transurethral resection, the patient was found to have a left distal ureteral mass and underwent left ureterectomy with partial cystectomy. Pathology again demonstrated clear cell RCC. RCC with solitary metastasis to the bladder is rare, and there are no targeted guideline recommendations for management. Per standard of care, patients with painless hematuria and risk factors for malignancy should undergo cystoscopy. In patients with a history of RCC, metastasis to the bladder should be considered in the differential diagnosis. Patients with metastatic RCC to the bladder should undergo a thorough work-up for additional sites of metastasis. In patients with RCC who develop solitary bladder metastasis amenable to resection following nephrectomy, there is a lack of evidence to guide therapy and a multidisciplinary discussion is warranted. However, if the tumor is amenable to resection, metastasectomy is a reasonable therapeutic approach and offers the patient an improved quality of life and an opportunity for remission.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"4339270"},"PeriodicalIF":0.0,"publicationDate":"2022-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40398441","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
Melanosis of the Bladder: Possible Pathogenetic Mechanisms. 膀胱黑色素病:可能的发病机制。
Pub Date : 2022-06-16 eCollection Date: 2022-01-01 DOI: 10.1155/2022/6221499
Justin E Dupey, Sarah J Wood, Richard Y Ball

Melanin accumulation within the bladder urothelium and/or macrophages in the lamina propria (melanosis of the bladder) is a very rare phenomenon of unknown pathogenesis. Its rarity argues for a complex, likely multifactorial, causation. We describe bladder melanosis developing after Botox therapy in an elderly woman with a history of overactive bladder, treated grade 2 uterovaginal prolapse, and episodes of urinary tract infection and speculate that one factor (probably of many) in its pathogenesis may be a derangement of local neurourothelial interactions.

黑色素积聚在膀胱尿路上皮和/或巨噬细胞固有层(膀胱黑色素病)是一种非常罕见的现象,其发病机制尚不清楚。它的罕见说明了一个复杂的,可能是多因素的原因。我们描述了一位患有膀胱过度活动、治疗过的2级子宫阴道脱垂和尿路感染的老年妇女,在肉毒杆菌治疗后发生膀胱黑色素瘤,并推测其发病机制的一个因素(可能是许多因素)可能是局部神经上皮相互作用的紊乱。
{"title":"Melanosis of the Bladder: Possible Pathogenetic Mechanisms.","authors":"Justin E Dupey,&nbsp;Sarah J Wood,&nbsp;Richard Y Ball","doi":"10.1155/2022/6221499","DOIUrl":"https://doi.org/10.1155/2022/6221499","url":null,"abstract":"<p><p>Melanin accumulation within the bladder urothelium and/or macrophages in the lamina propria (melanosis of the bladder) is a very rare phenomenon of unknown pathogenesis. Its rarity argues for a complex, likely multifactorial, causation. We describe bladder melanosis developing after Botox therapy in an elderly woman with a history of overactive bladder, treated grade 2 uterovaginal prolapse, and episodes of urinary tract infection and speculate that one factor (probably of many) in its pathogenesis may be a derangement of local neurourothelial interactions.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":" ","pages":"6221499"},"PeriodicalIF":0.0,"publicationDate":"2022-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225889/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40400155","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: 2
期刊
Case Reports in Urology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
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
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1