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Intranodal Ultrasound-Guided Percutaneous Methylene Blue Injection for the Identification of Leakage Point during Laparoscopic Repair of Refractory Chylous Ascites after Laparoscopic Lymphadenectomy for Kidney Cancer. 结内超声引导下经皮亚甲基蓝注射在肾癌腹腔镜淋巴结切除术后难治性乳糜腹水腹腔镜修复中渗漏点的识别。
Pub Date : 2022-11-21 eCollection Date: 2022-01-01 DOI: 10.1155/2022/3817554
Hugo Otaola-Arca, Patricio Vargas, Daniel Hasson, Marcelo Orvieto, Carmen Niño-Taravilla, Hugo Bermúdez

Chylous ascites is an uncommon complication after surgery that can result in malnutrition and immunodeficiency. Therefore, surgical interventions are reserved for refractory patients, and the primary success factor for these interventions is locating the point of leakage, which is often tricky. We describe a case of a 56-year-old male with chylous ascites after laparoscopic radical nephrectomy and lumbo-aortic lymphadenectomy for kidney cancer. The patient was initially managed with dietary modifications and drainage placement. Afterward, lymphography with Lipiodol, percutaneous embolization of the leakage point, and total parenteral nutrition were established. Finally, the patient underwent laparoscopic repair after identifying the leakage point by injecting methylene blue through an inguinal node. Complete resolution was achieved, and no complications related to the procedure were recorded. Intranodal methylene blue injection can be an invaluable tool to identify the point of leakage in selected patients to improve the outcomes of surgical repair of refractory chylous ascites.

乳糜腹水是一种罕见的术后并发症,可导致营养不良和免疫缺陷。因此,手术干预是为难治性患者保留的,这些干预的主要成功因素是定位渗漏点,这通常是棘手的。我们描述了一个56岁的男性乳糜腹水后腹腔镜根治性肾切除术和腰主动脉淋巴结切除术肾癌。患者最初通过调整饮食和放置引流管进行治疗。术后行脂醇淋巴造影、渗漏点经皮栓塞、全肠外营养。最后,患者通过腹股沟淋巴结注射亚甲基蓝确定渗漏点后,行腹腔镜修复。完全解决了问题,没有记录与手术相关的并发症。结内亚甲基蓝注射可以是一个宝贵的工具,以确定泄漏点的选定患者,以提高手术修复难治性乳糜腹水的结果。
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引用次数: 0
Crisis Averted: Clinical T1b Renal Mass with Concurrent Arteriovenous Malformation and Renal Vein Thrombus. 避免危机:临床T1b肾肿块并发动静脉畸形和肾静脉血栓。
Pub Date : 2022-11-17 eCollection Date: 2022-01-01 DOI: 10.1155/2022/9176199
David Zekan, Kareem Wasef, Zachary Werner, Robert Grammer, Cara Lombard, Adam Luchey, Ali Hajiran

Arteriovenous malformations (AVMs) secondary to renal-cell carcinoma (RCC) are well-described in the literature. Independently, renal vein and inferior vena cava tumor thrombi can be detected in locally-advanced RCC. A 67-year-old gentleman presented with a cT1b renal mass detected on workup for elevated creatinine. Multiphase CT imaging obtained for partial nephrectomy surgical-planning revealed an initially-missed renal cortical AVM. This drastically changed the plan for intervention, including use of an open approach with AVM embolization by interventional radiology prior and avoidance of a nephron-sparing approach. Final pathology confirmed the AVM and a subclinical renal vein thrombus masked by arterial flow on CT imaging, making this the first concurrent case described in the literature. Herein, we describe avoidance of catastrophic intraoperative hemorrhage by careful review of preoperative imaging and provide a literature review of imaging modalities for both renal surgical-planning and detection of tumor thrombi in RCC.

肾细胞癌(RCC)继发的动静脉畸形(AVMs)在文献中有很好的描述。局部晚期肾癌可单独检测到肾静脉和下腔静脉肿瘤血栓。一位67岁的男士在肌酐升高的检查中发现cT1b肾肿块。在部分肾切除术手术计划中获得的多期CT成像显示最初未发现的肾皮质AVM。这彻底改变了干预计划,包括通过介入放射学预先使用开放的AVM栓塞入路和避免保留肾单元的入路。最终病理证实AVM和亚临床肾静脉血栓在CT上被动脉血流掩盖,这是文献中第一例同时出现的病例。在此,我们描述了通过仔细检查术前影像学来避免灾难性术中出血,并提供了肾细胞癌中肾脏手术计划和肿瘤血栓检测的影像学方法的文献综述。
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引用次数: 0
A Rare Case of a Bladder Neck Abscess Masquerading as a Benign Mass. 膀胱颈部脓肿伪装成良性肿块一例。
Pub Date : 2022-10-04 eCollection Date: 2022-01-01 DOI: 10.1155/2022/9966553
Victor A Abdullatif, Jacob Novack, Philip J Shalhoub, Todd G Campbell, Joel E Abbott

Introduction: Bladder neck abscesses are rare urologic pathologies with very few cases published in modern literature. This report explores a case of a bladder neck mass incidentally found on computed tomography (CT) imaging in a patient with an iliopsoas abscess. Case Presentation. We present a case of a 60-year-old woman who was recently treated for sepsis secondary to an iliopsoas abscess in July of 2022. A CT scan revealed an indeterminate structure in the posterior inferior left paramedian bladder wall. During a cystoscopy with transurethral resection of the mass, an abscess was uncovered and evacuated. A postoperative Foley catheter was left in place, and the patient recovered without any complications.

Conclusion: At the time of publication, the patient feels well and denies pain or lower urinary tract symptoms. Although bladder abscesses are exceptionally rare, incidental findings during cystoscopy may warrant further investigation in patients with comorbid abscesses.

摘要膀胱颈脓肿是一种罕见的泌尿系统疾病,在现代文献中报道的病例很少。本报告探讨了一个病例膀胱颈部肿块偶然发现在计算机断层扫描(CT)成像的病人髂腰肌脓肿。案例演示。我们报告了一个60岁的女性病例,她最近在2022年7月因髂腰肌脓肿继发脓毒症接受了治疗。CT扫描显示膀胱左旁侧壁后下段结构不确定。在膀胱镜检查与经尿道切除肿块,脓肿被发现和疏散。术后留置Foley导尿管,患者恢复无任何并发症。结论:在发表时,患者感觉良好,否认疼痛或下尿路症状。虽然膀胱脓肿非常罕见,但膀胱镜检查时的偶然发现可能需要对合并脓肿的患者进行进一步的调查。
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引用次数: 0
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。
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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。
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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":null,"pages":null},"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":null,"pages":null},"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":null,"pages":null},"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":null,"pages":null},"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":null,"pages":null},"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
期刊
Case Reports in Urology
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