genitourinary tract

泌尿生殖道
  • 文章类型: Case Reports
    包虫囊肿病,由细粒棘球蚴幼虫形成,通常会影响肝脏,肺,和泌尿生殖道。该病例报告详细介绍了一名62岁男性的包虫囊肿的异常表现,该男性有膀胱后包虫囊肿手术史。病人出现阴茎根部疼痛,随后的成像显示耻骨上囊肿,耻骨,和左果胶肌肉区域。尽管COVID-19大流行带来了挑战,患者于2023年接受了手术切除.讨论强调了这种局部囊肿的罕见性,诊断成像技术,以及手术干预的必要性。术后期间涉及阿苯达唑的疗程。虽然直肠膀胱包虫囊肿并不常见,这一病例强调了在肿块鉴别诊断中考虑它们的重要性,特别是在流行地区。手术切除仍然是有症状的包虫囊肿的主要治疗方法。
    Hydatid cyst disease, caused by the Echinococcus granulosus tapeworm larval form, typically affects the liver, lungs, and genitourinary tract. This case report details an unusual manifestation of hydatid cysts in a 62-year-old male with a history of retrovesical hydatid cyst surgery. The patient presented with pain at the root of the penis, and subsequent imaging revealed cysts in the suprapubic, pubic bone, and left pectineus muscle regions. Despite the challenges posed by the COVID-19 pandemic, the patient underwent surgical excision in 2023. The discussion emphasizes the rarity of such localized cysts, diagnostic imaging techniques, and the necessity of surgical intervention. The postoperative period involved a course of albendazole. While rectovesical hydatid cysts are uncommon, this case underscores the importance of considering them in the differential diagnosis of masses, particularly in endemic regions. Surgical excision remains the primary treatment for symptomatic hydatid cysts.
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  • 文章类型: Journal Article
    神经内分泌癌(NECs)是低分化和高度侵袭性的上皮神经内分泌肿瘤。最常见的原发部位是肺,但是它们可能出现在每个器官中。大约37%的肺外NECs(EP-NECs)发生在胃肠胰腺(GEP)道,其次是泌尿生殖系统(GU)和妇科。由于它们的稀缺性,很少有证据来指导治疗建议,多学科方法对于此类患者的管理至关重要。基于铂的化疗目前代表了任何部位的EP-NEC的护理标准,反映了小细胞肺癌(SCLC)的管理,但进一步的方法仍在调查中。的确,正在进行的评估靶向治疗的试验,免疫检查点抑制剂(ICIs),和放射性核素治疗可以提供潜在的突破性治疗选择。鉴于这些孤儿疾病的循证文献相对缺乏,这篇综述的目的是提供病理学和当前治疗方案的概述,以及阐明该领域最紧迫的未满足需求。
    Neuroendocrine carcinomas (NECs) are poorly differentiated and highly aggressive epithelial neuroendocrine neoplasms. The most common primary site is the lung, but they may arise in every organ. Approximately 37% of extrapulmonary NECs (EP-NECs) occur in the gastroenteropancreatic (GEP) tract, followed by the genitourinary (GU) system and gynecological tract. As a result of their rarity, there is scant evidence to guide treatment recommendations, and a multidisciplinary approach is essential for the management of such patients. Platinum-based chemotherapy currently represents the standard of care for EP-NECs of any site, mirroring the management of small-cell lung cancer (SCLC), but further approaches are still under investigation. Indeed, ongoing trials evaluating targeted therapies, immune checkpoint inhibitors (ICIs), and radionuclide therapy could provide potentially breakthrough therapeutic options. Given the relative dearth of evidence-based literature on these orphan diseases, the aim of this review is to provide an overview of the pathology and current treatment options, as well as to shed light on the most pressing unmet needs in the field.
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  • 文章类型: Journal Article
    目的:泌尿生殖道小细胞癌(GUSCC)是一种罕见的疾病,预后不良。由于对疾病的了解不足,因此只有有限的治疗选择。在这项研究中,我们分析了GUSCC患者的临床结局及其与肿瘤免疫表型的关系.
    方法:纳入诊断为GUSCC的患者。根据原发位置(前列腺和非前列腺)和分期(局限性疾病[LD]和广泛疾病[ED])分析生存结果。我们在非前列腺SCC患者中进行了多重免疫组织化学(IHC),并分析了免疫细胞群。
    结果:本研究共纳入77例患者。他们的平均年龄是71岁,67例(87.0%)为男性,48例患者(62.3%)有非前列腺SCC。所有ED患者(n=31,40.3%)接受依托泊苷加铂(EP)作为初始治疗,中位总生存期(OS)为9.7个月(95%置信区间[CI],7.1to18.6).LD患者(n=46,59.7%)接受EP,然后放疗或手术,24个月OS率为63.6%(95%CI,49.9~81.0)。对21例非前列腺SCC患者的多重IHC分析显示,表达CD68+CD206+M2样巨噬细胞的程序性死亡配体1密度较高的患者的OS结果明显较差,调整后的风险比为4.17(95%CI,1.25至14.29;调整后的p=0.02)。
    结论:GUSCC患者预后不良,甚至那些患有局部疾病的人。肿瘤免疫表型与生存率显著相关。这一发现为治疗GUSCC提供了新的见解。
    OBJECTIVE: Small cell carcinoma of the genitourinary tract (GU SCC) is a rare disease with a poor prognosis. There are only limited treatment options due to insufficient understanding of the disease. In this study, we analyzed the clinical outcomes of patients with GU SCC and their association with the tumor immune phenotype.
    METHODS: Patients diagnosed with GU SCC were included. Survival outcomes according to the primary location (prostate and non-prostate) and stages (limited disease [LD] and extensive disease [ED]) were analyzed. We performed multiplex immunohistochemistry (IHC) in non-prostate SCC patients and analyzed the immune cell population.
    RESULTS: A total of 77 patients were included in this study. Their median age was 71 years, 67 patients (87.0%) were male, and 48 patients (62.3%) had non-prostate SCC. All patients with ED (n=31, 40.3%) received etoposide plus platinum (EP) as initial treatment and median overall survival (OS) was 9.7 months (95% confidence interval [CI], 7.1 to 18.6). Patients with LD (n=46, 59.7%) received EP followed by radiotherapy or surgery, and 24-months OS rate was 63.6% (95% CI, 49.9 to 81.0). The multiplex IHC analysis of 21 patients with non-prostate SCC showed that patients with a higher density of programmed death-ligand 1-expressing CD68+CD206+ M2-like macrophages had significantly worse OS outcomes with an adjusted hazards ratio of 4.17 (95% CI, 1.25 to 14.29; adjusted p=0.02).
    CONCLUSIONS: Patients with GU SCC had a poor prognosis, even those with localized disease. The tumor immune phenotypes were significantly associated with survival. This finding provides new insights for treating GU SCC.
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  • 文章类型: Journal Article
    孤立性纤维性肿瘤(SFT)是一种具有可变行为的间充质肿瘤,很少涉及泌尿生殖道(GU)。大多数报告的病例对应于孤立的病例报告。STAT6免疫组织化学是较新和可靠的诊断标记。在两个大专院校的病理学数据库中搜索了涉及GU道的SFT。STAT6强弥漫性核染色证实了所有四例病例的诊断,NGS证实NAB2::STAT6融合1例。2例经穿刺活检确诊,一个涉及前列腺,另一个涉及精囊。一例对应于与前列腺和膀胱密不可分并浸润的盆腔肿块。其余代表精索极为罕见。在涉及GU器官的梭形细胞病变的鉴别诊断中,应考虑SFT的参与。STAT6强弥漫性核染色是重要的辅助工具,特别是在活检中。
    Solitary fibrous tumour (SFT) is a mesenchymal neoplasm with variable behaviour, very rarely involving the genitourinary (GU) tract. Most reported cases correspond to isolated case reports. STAT6 immunohistochemistry is a more recent and reliable diagnostic marker. The pathology database of two tertiary institutes was searched for SFTs involving the GU tract. STAT6 strong diffuse nuclear staining confirmed the diagnosis in all four cases, and the NAB2::STAT6 fusion was demonstrated by NGS in one case. Two cases were diagnosed in needle biopsy, one involving the prostate and the other involving the seminal vesicle. One case corresponded to a pelvic mass inseparable from and infiltrating the prostate and bladder. The remainder represented an exceedingly rare involvement of the spermatic cord. Involvement by a SFT should be considered in the differential diagnosis of spindle cell lesions involving GU organs. STAT6 strong diffuse nuclear staining is an important ancillary tool, particularly in a biopsy.
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  • 文章类型: Journal Article
    凭借通过专用后处理算法提供的材料区分能力,双能量CT(DECT)已被证明在评估各种疾病方面具有优势。在这篇文章中,我们回顾了DECT在泌尿生殖系统疾病评估中的诊断应用,强调其在肾结石表征中的作用,偶发性肾和肾上腺病变表征,腹膜后创伤,减少辐射,以及造影剂剂量和成本效益潜力。我们还讨论了DECT扫描模式的未来前景,包括使用新的造影剂注射策略和光子计数探测器计算机断层扫描。
    By virtue of material differentiation capabilities afforded through dedicated postprocessing algorithms, dual-energy CT (DECT) has been shown to provide benefit in the evaluation of various diseases. In this article, we review the diagnostic use of DECT in the assessment of genitourinary diseases, with emphasis on its role in renal stone characterization, incidental renal and adrenal lesion characterization, retroperitoneal trauma, reduction of radiation, and contrast dose and cost-effectiveness potential. We also discuss future perspectives of the DECT scanning mode, including the use of novel contrast injection strategies and photon-counting detector computed tomography.
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  • 文章类型: Journal Article
    肾源性腺瘤(NA)是一种罕见的化生实体,通常与先前的尿路上皮损伤有关。大多数见于膀胱,少数见于尿道。在这项研究中,我们评估了p16作为该实体的替代标志物的表达,并将其与临床病理参数相关联。回顾性研究了17例NA,以评估p16的免疫组织化学表达及其对该实体的诊断价值。
    Nephrogenic adenoma (NA) is a rare metaplastic entity commonly associated with a prior urothelial injury. Most are seen in the urinary bladder and a minority involve the urethra. In this study, we evaluated the expression of p16 as a surrogate marker of this entity and correlated it with clinical pathological parameters. A total of 17 cases of NA were retrospectively studied to assess the immunohistochemical expression of p16 and its value for the diagnosis of this entity.
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  • 文章类型: Systematic Review
    背景:肾脏是泌尿生殖系统中最常受损的组成部分,占所有创伤病例的5%。不同社会的一些指南解决了泌尿系统创伤的管理。然而,关于在血流动力学稳定的患者中血管栓塞的最佳使用仍未解决的问题,在血流动力学不稳定的情况下,对稳定的腹膜后血肿和肾脏抢救技术进行手术探查的指征,以及接受非手术治疗的患者的影像学实践。我们进行了系统的审查,荟萃分析,并制定了基于证据的建议来回答钝性和穿透性肾损伤中的这些问题。
    方法:工作组制定了四个人口,干预,比较器,结果(PICO)关于以下主题的问题:(1)血管栓塞(AE)在有持续出血证据的血液动力学稳定患者中的使用;(2)稳定区II血肿的手术方法(探索与无探查)在血流动力学不稳定的患者和(3)手术技术(肾切除术与肾脏保存)用于血流动力学不稳定患者的II区血肿扩大;(4)高度创伤性肾损伤中重复成像(常规或基于症状)的频率。对现有证据进行系统评价和荟萃分析。使用RevMan5(Cochran协作)和GRADepro(等级工作组)软件。工作组成员对建议进行了表决,并对每项最终建议表示同意。
    结果:共鉴定和分析了20篇文章。遇到了两项前瞻性研究;大多数是回顾性的,单一机构研究。并非所有研究都报告了PICO问题预测的所有结果。对所有PICO问题进行荟萃分析,但PICO3继发于这些研究中包含的不同患者群体。PICO1在9项研究的荟萃分析中纳入了最多的文章;然而,由于研究设计的差异,没有出现关键结局;在一组较小的文章中,类似的差异阻碍了对PICO4关键结局的观察.对PICOs2和3的分析支持符合当前国际实践趋势的非侵入性或微创方法。
    结论:在血液动力学稳定的成年患者中,临床或影像学证据表明持续出血,没有关于AE与AE的作用的建议观察。在血流动力学不稳定的成年患者中,我们有条件地建议没有肾探查与稳定区Ⅱ血肿肾探查术。在血流动力学不稳定的成年患者中,我们有条件地推荐肾脏保存技术与II区血肿扩大的肾切除术。无法推荐在高度肾损伤中重复成像的最佳时机。
    方法:指南;系统综述,三级。
    BACKGROUND: The kidney is the most frequently injured component of the genitourinary system, accounting for 5% of all trauma cases. Several guidelines by different societies address the management of urological trauma. However, unanswered questions remain regarding optimal use of angioembolization in hemodynamically stable patients, indications for operative exploration of stable retroperitoneal hematomas and renal salvage techniques in the setting of hemodynamic instability, and imaging practices for patients undergoing non-operative management. We performed a systematic review, meta-analysis, and developed evidence-based recommendations to answer these questions in both blunt and penetrating renal trauma.
    METHODS: The working group formulated four population, intervention, comparator, outcome (PICO) questions regarding the following topics: (1) angioembolization (AE) usage in hemodynamically stable patients with evidence of ongoing bleeding; (2) surgical approach to stable zone II hematomas (exploration vs. no exploration) in hemodynamically unstable patients and (3) surgical technique (nephrectomy vs. kidney preservation) for expanding zone II hematomas in hemodynamically unstable patients; (4) frequency of repeat imaging (routine or symptom based) in high-grade traumatic renal injuries. A systematic review and meta-analysis of currently available evidence was performed. RevMan 5 (Cochran Collaboration) and GRADEpro (Grade Working Group) software were used. Recommendations were voted on by working group members and concurrence was obtained for each final recommendation.
    RESULTS: A total of 20 articles were identified and analyzed. Two prospective studies were encountered; the majority were retrospective, single-institution studies. Not all outcomes projected by PICO questions were reported in all studies. Meta-analysis was performed for all PICO questions except PICO 3 secondary to the discrepant patient populations included in those studies. PICO 1 had the greatest number of articles included in the meta-analysis with nine studies; yet, due to differences in study design, no critical outcomes emerged; similar differences among a smaller set of articles prevented observation of critical outcomes for PICO 4. Analyses of PICOs 2 and 3 favored a non-invasive or minimally invasive approach in-line with current international practice trends.
    CONCLUSIONS: In hemodynamically stable adult patients with clinical or radiographic evidence of ongoing bleeding, no recommendation could be made regarding the role of AE vs. observation. In hemodynamically unstable adult patients, we conditionally recommend no renal exploration vs. renal exploration in stable zone II hematomas. In hemodynamically unstable adult patients, we conditionally recommend kidney preserving techniques vs. nephrectomy in expanding zone II hematomas. No recommendation could be made for the optimal timing of repeat imaging in high grade renal injury.
    METHODS: Guideline; systematic review, level III.
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  • 文章类型: Case Reports
    尾重复综合征(CDS)是一种罕见的先天性异常,其中广泛的畸形,从胃肠道(GIT)的部分或孤立的尾器官完全重复,泌尿生殖道(GUT),和脊髓和神经系统发生。确切原因不明,然而,在CDS的病因中提到了各种因素,如遗传性疾病和联合孪生。孕中期异常扫描可以在产前诊断这种异常。此病例报告描述了一名患有CDS的初生患者,没有任何神经系统症状。她通过剖宫产生下了一个健康的女婴,并以臀位为适应症。
    Caudal duplication syndrome (CDS) is a rare congenital anomaly in which a wide spectrum of malformations ranging from partial or isolated to complete duplication of caudal organs in the gastrointestinal tract (GIT), genitourinary tract (GUT), and spinal and neural systems occur. Its exact cause is unknown, however various factors such as genetic disorders and conjoined twinning are mentioned in the etiology of CDS. Second-trimester anomaly scan can diagnose this anomaly prenatally. This case report describes a primi postnatal patient with CDS without any neurological symptoms. She gave birth to a healthy baby girl by cesarean section with breech presentation as an indication.
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  • 天然治疗微生物提供了一个有效的替代医疗保健治疗,如今,具有预防多种人类疾病的潜力。这些促进健康的生物,益生菌大多属于革兰氏阳性菌,如乳杆菌,双歧杆菌,链球菌,酵母菌,芽孢杆菌和肠球菌。大约一个世纪前开始,益生菌的应用已经走了很长的路。本综述集中于益生菌在改善多种感染中的潜在治疗作用。如上呼吸道感染和病毒性呼吸道感染,包括Covid-19;肝病和肝性脑病;神经和精神疾病;自身免疫性疾病,尤其是类风湿性关节炎,系统性红斑狼疮和多发性硬化症。除了这些,益生菌在尿路感染中的治疗恶化是非常有希望的,并在这里回顾和介绍了几种方法。我们还介绍了即将到来的和新的重点领域,益生菌治疗干预措施显示出有希望的结果,比如粪便微生物移植和阴道微生物移植.
    Natural therapeutic microorganisms provide a potent alternative healthcare treatment nowadays, with the potential to prevent several human diseases. These health-boosting living organisms, probiotics mostly belong to Gram-positive bacteria such as Lactobacillus, Bifidobacterium, Streptococcus, Saccharomyces, Bacillus and Enterococcus. Initiated almost a century ago, the probiotic application has come a long way. The present review is focused on the potential therapeutic role of probiotics in ameliorating multiple infections, such as upper respiratory tract infections and viral respiratory infections, including COVID-19; liver diseases and hepatic encephalopathy; neurological and psychiatric disorders; autoimmune diseases, particularly rheumatoid arthritis, systemic lupus erythematosus and multiple sclerosis. Apart from these, the therapeutic exacerbations of probiotics in urinary tract infections have been extremely promising, and several approaches are reviewed and presented here. We also present upcoming and new thrust areas where probiotic therapeutic interventions are showing promising results, like faecal microbial transplant and vaginal microbial transplant.
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  • 文章类型: Case Reports
    生殖器结核在包括克罗地亚在内的欧洲国家是一种罕见且意外的疾病。女性生殖道结核的诊断具有挑战性,并且由于其特异性低,很少被临床症状指出。作者决定在一名年轻人中提出一例泌尿生殖系统结核病,临床高度怀疑腹部肿瘤肿块的免疫能力好的妇女。虽然被认为是对过去的厌恶,应预期并考虑生殖器结核的罕见临床表现。
    Genital tuberculosis is a rare and unexpected disease in European countries including Croatia. Diagnosis of female genital tract tuberculosis is challenging and is rarely pin-pointed by clinical symptoms because of their low specificity. The authors decided to present a case of genitourinary tuberculosis in a young, immunocompetent fertile woman with high clinical suspicion of abdominal tumor mass. Although considered a desease of the past, rare clinical presentation of genital tuberculosis should be expected and taken into account.
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