• 文章类型: Journal Article
    关于载脂蛋白(Apos)与勃起功能障碍(ED)之间关联的现有研究主要依赖于观察性研究,并且在诊断ED时没有区分器质性和精神性原因。很难相信Apos在心理性ED中起作用。为了解决这些问题,我们的研究使用孟德尔随机化(MR)分析探讨了脂蛋白与ED之间的因果关系,并通过使用夜间阴茎肿胀和僵硬(NPTR)监测来区分器质性和心理性ED.多变量MR分析显示高密度脂蛋白(HDL),ApoA1和ApoB/A1伴ED(OR和95%CI为0.33(0.14-0.78),3.58(1.52-8.43),和0.30(0.13-0.66))。我们使用多变量分析和受试者工作特征(ROC)曲线对212例患者的数据进行了统计和分析.器质性ED患者的HDL水平明显降低,ApoA1和ApoA1/B,而器质性ED患者的ApoB和低密度脂蛋白(LDL)水平明显更高。采用ROC曲线评价Apos预测器质性ED风险的诊断价值。结果表明,ApoA1和ApoA1/B表现出良好的预测价值。HDL,在我们的研究中,ApoA1和ApoA1/B已被确定为ED的危险因素。此外,我们的研究强调了ApoA1和ApoA1/ApoB在有机ED开发中的重要性,并建议将其用作评估与有机ED相关风险的指标.
    The existing research on the association between apolipoproteins (Apos) and erectile dysfunction (ED) primarily relies on observational studies and does not distinguish between organic and psychogenic causes when diagnosing ED. It is difficult to believe that Apos play a role in psychogenic ED. To address these issues, our study explored the causal relationship between lipoproteins and ED using Mendelian randomization (MR) analysis and differentiate between organic and psychogenic ED through the use of nocturnal penile tumescence and rigidity (NPTR) monitoring. Multivariate MR analysis revealed significant causal associations between high-density lipoprotein (HDL), Apo A1, and Apo B/A1 with ED (OR and 95% CI were 0.33 (0.14-0.78), 3.58 (1.52-8.43), and 0.30 (0.13-0.66)). we conducted statistical and analytical analyses on the data of 212 patients using multivariate analyses and receiver operating characteristic (ROC) curves. Patients with organic ED had significantly lower levels of HDL, Apo A1 and Apo A1/B, whereas patients with organic ED had considerably higher levels of Apo B and low-density lipoprotein (LDL). The diagnostic value of Apos in predicting the risk of organic ED was evaluated using ROC curves. The results indicated that Apo A1 and Apo A1/B demonstrated good predictive value. HDL, Apo A1, and Apo A1/B have been identified as risk factors for ED in our study. Furthermore, our research highlights the significance of Apo A1 and Apo A1/Apo B in the development of organic ED and suggests their potential use as indicators to assess the risks associated with organic ED.
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  • 文章类型: Case Reports
    海绵状神经及其分支的医源性损伤导致多达85%的接受根治性前列腺切除术的男性术后勃起功能障碍。这里,我们描述了使用一种新颖的荧光成像系统来检测一位66岁的前列腺腺癌绅士的神经自发荧光(格里森评分8[44],预后组4,表明高度侵袭性前列腺癌)接受了腹腔镜根治性前列腺切除术。
    方法:在全身麻醉下,使用标准手术技术进行了腹腔镜前列腺癌根治术.手术期间,a树突成像相机(树突®成像,德国)被用来允许手术团队在标准手术室(白色)光和近紫外线(NUVL)之间自由切换,为了增强前列腺周围神经丛的可视化,包括海绵状神经及其所有分支.在白光下,海绵状神经或其任何分支都不清晰可见。然而,在NUVL下,所有荧光都发出明亮的荧光,在前列腺切除术期间很容易避免。前列腺切除术进行,没有术中或术后并发症。此外,在外科诊所进行了一个月的随访,患者报告无勃起功能障碍,排尿困难,或其他神经系统或非神经系统疾病。
    在这种情况下,根治性前列腺切除术期间海绵体神经及其分支的自发荧光有助于其可视化,并且似乎有助于预防术后勃起功能障碍和所有其他潜在的神经功能缺损。
    结论:使神经能够自动发荧光的新型术中技术值得进行更大的系列和比较试验,以评估其在前列腺癌根治术中减少医源性神经损伤的有效性。
    UNASSIGNED: Iatrogenic injury to the cavernous nerve and its branches results in post-operative erectile dysfunction in up to 85 % of men undergoing a radical prostatectomy. Here, we describe using a novel fluorescence-imaging system developed to detect nerve autofluorescence in a 66-year-old gentleman with prostate adenocarcinoma (Gleason Score 8 [4 + 4], prognostic group 4, indicating a highly-aggressive prostate cancer) who underwent laparotomic radical prostatectomy.
    METHODS: Under general anesthesia, a laparotomic radical prostatectomy was performed using standard operative techniques. During surgery, a Dendrite imaging camera (Dendrite® Imaging, Germany) was employed to permit the surgical team to toggle freely between standard operating room (white) light and near-ultraviolet light (NUVL), with the specific purpose of enhancing visualization of the periprostatic nerve plexus, including the cavernous nerve and all its branches. Under white light, neither the cavernous nerve nor any of its branches were clearly visible. However, under NUVL, all fluoresced brightly and were easily avoided during prostate resection. Prostate resection proceeded with no intra-operative or post-operative complications. Moreover, upon one-month follow-up in the surgery clinic, the patient reported no erectile dysfunction, difficulties voiding, or other neurological or non-neurological complaints.
    UNASSIGNED: In this case, autofluorescence of the cavernous nerve and its branches during radical prostatectomy aided in their visualization and appeared to help prevent post-operative erectile dysfunction and all other potential neurological deficits.
    CONCLUSIONS: Novel intra-operative technology enabling nerves to auto-fluoresce warrants larger series and comparative trials to assess its effectiveness reducing iatrogenic nerve injury during radical prostatectomies.
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  • 文章类型: Case Reports
    背景:原发性睾丸淋巴瘤(PTL)相对罕见。对侧睾丸是PTL复发的常见部位;因此,一旦达到完全缓解,对侧睾丸进行放射治疗(RT)以防止复发。
    方法:一名76岁男性被诊断患有PTL并接受如上所述的RT。然而,尽管实现并保持完全缓解,经组织活检诊断为弥漫性大B细胞淋巴瘤的包块在预防性RT后6.5年在龟头出现。我们使用从两个组织病理学标本中提取的DNA的下一代测序,通过基因组分析,研究了龟头阴茎淋巴瘤是PTL复发还是新的恶性肿瘤。
    结论:我们在四个体细胞基因中发现了相同的变异等位基因分数(MYD88,IL7R,BLNK,和FLT3)在相似的频率下,这表明阴部阴茎淋巴瘤与PTL的起源相同。据我们所知,这是首例龟头PTL复发的病例报告.
    BACKGROUND: Primary testicular lymphoma (PTL) is relatively rare. The contralateral testis is a common site of PTL relapse; therefore, once complete remission is achieved, radiation therapy (RT) is administered to the contralateral testis to prevent relapse.
    METHODS: A 76-year-old man was diagnosed with PTL and received RT as described above. However, despite achieving and maintaining complete remission, a mass diagnosed as diffuse large B-cell lymphoma by tissue biopsy developed in the glans penis 6.5 years after prophylactic RT. We investigated whether the glans penile lymphoma was PTL relapse or a new malignancy by genomic analysis using next-generation sequencing of DNA extracted from two histopathological specimens.
    CONCLUSIONS: We found the same variant allele fraction in four somatic genes (MYD88, IL7R, BLNK, and FLT3) at similar frequencies, indicating that the glans penile lymphoma had the same origin as the PTL. To the best of our knowledge, this is the first case report of PTL relapse in the glans penis.
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  • 文章类型: Case Reports
    Noonan综合征(NS)是一种遗传性疾病,其特征是由RAS/丝裂原激活的蛋白激酶通路突变引起的多种先天性缺陷。据报道,NS的男性生育能力受到损害,但只有少数研究关注NS患者的生育状况,潜在机制仍未完全了解.我们描述了一名35岁男子因勃起功能障碍和严重的少精症而接受了男性学评估的情况。临床检查出现综合征性面部外观和睾丸大小减小。激素评估显示总睾酮水平正常,高FSH水平,正常的低AMH和抑制素B,与原发性支持细胞功能障碍相容。遗传分析表明致病杂合变异c.742G>A,LZTR1基因(NM_006767.3)的p.(Gly248Arg)。此病例报告提供了有关NS男性原发性性腺功能障碍的更多知识,并从新基因LZTR1的罕见变异中丰富了NS的临床谱。
    Noonan syndrome (NS) is a genetic disorder characterized by multiple congenital defects caused by mutations in the RAS/mitogen-activated protein kinase pathway. Male fertility has been reported to be impaired in NS, but only a few studies have focused on fertility status in NS patients and underlying mechanisms are still incompletely understood. We describe the case of a 35-year-old man who underwent an andrological evaluation due to erectile dysfunction and severe oligospermia. A syndromic facial appearance and reduced testis size were present on clinical examination. Hormonal evaluation showed normal total testosterone level, high FSH level, and low-normal AMH and inhibin B, compatible with primary Sertoli cell dysfunction. Genetic analysis demonstrated the pathogenetic heterozygous variant c.742G>A, p.(Gly248Arg) of the LZTR1 gene (NM_006767.3). This case report provides increased knowledge on primary gonadal dysfunction in men with NS and enriches the clinical spectrum of NS from a rare variant in the novel gene LZTR1.
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  • 文章类型: Case Reports
    与更普遍的软组织肉瘤相比,罕见肉瘤由于有限的治疗选择和对其生物学的了解不足而提出了重大的治疗挑战。这项研究调查了一个独特的阴茎肉瘤病例,提供全面的形态学和分子分析。通过创建实验性患者衍生模型,包括患者衍生异种移植物(PDX),3D,和单层原代培养-我们成功复制了在患者肿瘤中观察到的关键分子特征,如平滑肌肌动蛋白和CD99表达,以及TSC2和FGFR4等基因的特定突变。这些模型有助于评估深入探索这种肿瘤生物学的潜力。这种全面的方法有望确定治疗这种极为罕见的软组织肉瘤的潜在治疗途径。
    Rare sarcomas present significant treatment challenges compared to more prevalent soft tissue sarcomas due to limited treatment options and a poor understanding of their biology. This study investigates a unique case of penile sarcoma, providing a comprehensive morphological and molecular analysis. Through the creation of experimental patient-derived models-including patient-derived xenograft (PDX), 3D, and monolayer primary cultures-we successfully replicated crucial molecular traits observed in the patient\'s tumor, such as smooth muscle actin and CD99 expression, along with specific mutations in genes like TSC2 and FGFR4. These models are helpful in assessing the potential for an in-depth exploration of this tumor\'s biology. This comprehensive approach holds promise in identifying potential therapeutic avenues for managing this exceedingly rare soft tissue sarcoma.
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  • 文章类型: Case Reports
    从肾细胞癌(RCC)或任何其他原发癌部位转移到阴茎是不寻常的;当它确实发生时,它通常涉及多个器官。一名75岁的男子出现阴茎疼痛和肿胀。三个月前,他接受了开放性根治性肾切除术和血栓切除术,并被诊断为透明细胞肾细胞癌合并下腔静脉肿瘤血栓形成。随访影像提示阴茎转移,由于疼痛加剧,导致全阴茎切除术。切除的肿块显示出与转移性RCC一致的特征。这个病例强调需要考虑罕见的转移部位,如RCC转移到阴茎,在RCC患者中。
    Metastasis to the penis from renal cell carcinoma (RCC) or any other primary cancer site is unusual; when it does occur, it often involves multiple organs. A 75-year-old man presented with penile pain and swelling. Three months earlier, he had open radical nephrectomy with thrombectomy and was diagnosed with clear-cell RCC with tumor thrombosis in the inferior vena cava. The follow-up imaging indicated metastasis to the penis, prompting a total penectomy due to worsening pain. The excised mass displayed features consistent with metastatic RCC. This case underscores the need to consider rare metastatic sites, such as the metastasis of RCC to the penis, in RCC patients.
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  • DOI:
    文章类型: Case Reports
    一例因性交不成功导致阴茎骨折的临床病例,后来需要以开放和引流血肿的身体成形术形式进行手术治疗,在文章中讨论。阴茎骨折是一种罕见的泌尿外科急症,需要立即就医以避免长期并发症,包括阴茎弯曲和勃起功能障碍。
    A clinical case of a penile fracture as a result of an unsuccessful sexual intercourse, which later required surgical treatment in the form of corporoplasty with opening and draining of the hematoma, is discussed in the article. Penile fracture is a rare urological emergency that requires immediate medical attention to avoid long-term complications, including penile curvature and erectile dysfunction.
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  • 文章类型: Case Reports
    阴茎骨折,虽然罕见,由于其潜在的严重后果,需要紧急手术治疗。此病例报告说明了及时,全面的影像学检查与手术探查在治疗双阴茎骨折的延迟表现中的重要性。
    方法:一名27岁男性在睡眠时阴茎受伤,创伤后36小时提交给我们的部门。他的临床症状包括明显的阴茎肿胀,偏差,和特征的“茄子”畸形。超声检查显示阴茎底部广泛的皮下水肿和大量血肿,白膜破裂。手术探查发现海绵体有两个明显的骨折,已成功修复。患者经历了快速且无并发症的恢复,在四天内恢复完整的勃起功能。
    该病例强调了阴茎骨折的解剖复杂性。尽管延误了求医,结果是有利的,挑战立即手术对于避免长期并发症至关重要的观念。文献表明,延迟手术可能不会显著影响长期结果,尤其是在没有尿道受累的情况下,我们的案例调查结果支持的观点。
    结论:阴茎骨折需要细致的诊断和治疗方法。该案例表明,尽管立即进行手术干预是理想的,在某些条件下,延迟修复也可能导致积极的结果。该报告有助于越来越多的证据表明,有可能重新评估当前的阴茎骨折治疗临床指南。
    UNASSIGNED: Penile fractures, though rare, demand urgent surgical attention due to their potentially severe consequences. This case report illustrates the significance of prompt and comprehensive imaging with surgical exploration in managing a delayed presentation of a double penile fracture.
    METHODS: A 27-year-old male sustained a penile injury during sleep, presenting to our department 36 h post-trauma. His clinical symptoms included significant penile swelling, deviation, and the characteristic \'eggplant\' deformity. Ultrasonography revealed extensive subcutaneous edema and a substantial hematoma at the penile base, with a disruption in the tunica albuginea. Surgical exploration identified two distinct fractures in the corpora cavernosa, which were successfully repaired. The patient experienced a rapid and complication-free recovery, regaining full erectile function within four days.
    UNASSIGNED: This case underlines the anatomical complexity of penile fractures. Despite the delay in seeking medical attention, the outcome was favorable, challenging the notion that immediate surgery is crucial for avoiding long-term complications. The literature suggests that delayed surgery might not significantly impact long-term outcomes, especially in the absence of urethral involvement, a perspective supported by our case findings.
    CONCLUSIONS: Penile fracture requires a nuanced approach to diagnosis and treatment. The case demonstrates that while immediate surgical intervention is ideal, delayed repair can also result in positive outcomes under certain conditions. This report contributes to the growing body of evidence suggesting the potential for re-evaluating current clinical guidelines for penile fracture management.
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  • DOI:
    文章类型: Review
    目的:探讨阴茎角化棘皮瘤(KA)的临床特点及治疗方案。
    方法:报告我院收治的1例阴茎角化棘皮瘤的诊治情况并复习文献。
    结果:患者因发现龟头新病变4个月而入院,“被诊断患有阴茎肿瘤,接受了肿瘤切除手术,组织病理学检查显示鳞状上皮增生,增厚,和过度角质化。术后病理诊断为阴茎角化棘皮瘤。随访期间无复发或转移。
    结论:KA是一种相对罕见的良性肿瘤,具有潜在的恶性转化,术后密切随访是必要的。
    OBJECTIVE: To explore the clinical characteristics and treatment options of keratoacanthoma (KA) of the penis.
    METHODS: We report the diagnosis and treatment of a case of penile keratoacanthoma in our hospital and review the literature.
    RESULTS: The patient was admitted due to the discovery of a \"new lesion on the glans for 4 months,\" diagnosed with a penile tumor, underwent tumor resection surgery, with histopathological examination revealing squamous epithelial hyperplasia, thickening, and excessive keratinization. The postoperative pathological diagnosis was penile keratoacanthoma. There was no recurrence or metastasis during follow-up.
    CONCLUSIONS: KA is a relatively rare benign tumor with potential malignant transformation, and close follow-up is necessary postoperatively.
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  • 文章类型: Case Reports
    暂无摘要。
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