Prostate

前列腺
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    文章类型: Case Reports
    最近,已经报道了局部治疗对转移性前列腺癌(PC)患者肿瘤结局的有效性.我们对前列腺局部孤立性病变缩小的患者进行了高强度聚焦超声(HIFU)半消融,诊断为磁共振成像(MRI)-经直肠超声融合图像引导的目标活检PSA水平为0.24ng/mL,在雄激素受体信号抑制剂(ARSI)和转移性PC的化疗后。治疗后1个月,前列腺特异性抗原水平降至0.01ng/mL,MRI上癌症可疑病灶消失。在24个月的随访中,PSA水平没有升高,没有与治疗相关的严重并发症。HIFU有可能成为一种有效的微创治疗方法,可作为ARSI和转移性PC化疗后前列腺局部缩小的孤立性病变的局部治疗方法。
    Recently, effectiveness of local treatment for oncological outcomes for patients with metastatic prostate cancer (PC) has been reported. We performed hemi-ablation with high-intensity focused ultrasound (HIFU) for a patient with a localized reducted solitary lesion in the prostate, which was diagnosed with magnetic resonance imaging (MRI)-transrectal ultrasound fusion image-guided target biopsy with PSA level of 0.24 ng/mL, after androgen receptor signaling inhibitors (ARSIs) and chemotherapy for metastatic PC. Prostate specific antigen levels decreased to 0.01ng/mL at 1 month after the treatment, and cancer suspicious lesion disappeared on MRI. During the follow-up of 24 months, there was no elevation of PSA level with no severe complication related to the treatment. HIFU has possibility to be an effective and minimally invasive treatment as a local treatment for the localized reducted solitary lesion in the prostate after ARSIs and chemotherapy for metastatic PC.
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  • 文章类型: Case Reports
    背景:膀胱原位癌是一种高级别癌症,起源于膀胱的浅层。它有可能侵入附近的器官,它可以通过血液和淋巴循环传播到身体的远处。
    方法:一名58岁非吸烟者男性表现为肉眼和显微镜下血尿。他的家族史包括他父亲最近的膀胱癌。初步调查显示血尿,炎症,尿培养阴性,直肠指检显示前列腺右叶增大,前列腺特异性抗原水平升高。取自膀胱粘膜和前列腺的样品的组织病理学检查证实膀胱和前列腺中的尿路上皮原位癌。进一步评估显示没有其他转移。肿瘤分类为T4aN0M0。患者接受了根治性膀胱前列腺切除术,组织病理学检查显示肿瘤侵犯了膀胱固有肌层以及前列腺,但是在前列腺尿道和其他区域没有发现恶性肿瘤。患者在术后三周出院,并完成了由吉西他滨组成的辅助化疗,和顺铂预防复发。患者目前健康状况良好。
    结论:膀胱癌转移到前列腺而不累及前列腺尿道的发生并不常见,需要精确的诊断技术来进行准确的肿瘤分类。建议早期治疗以提高患者的预后。
    BACKGROUND: Carcinoma in situ of the bladder is a high-grade cancer that originates in the superficial layer of the bladder. It has the potential to invade nearby organs, and it can spread through blood and lymphatic circulation to distant parts of the body.
    METHODS: A 58-year-old non-smoker male presented with gross and microscopic hematuria. His family history included his father\'s recent bladder cancer. Initial investigations showed hematuria, inflammation, negative urine culture, digital rectal examination revealed an enlarged right lobe of the prostate, and an elevated Prostate-Specific Antigen level. Histopathological examination of samples taken from the bladder mucosa and the prostate confirmed urothelial carcinoma in situ in the bladder and prostate. Further evaluation revealed no other metastasis. The tumor was classified as T4aN0M0. The patient underwent radical cystoprostatectomy and histopathological examination showed that the tumor invading the muscularis propria of the bladder as well as the prostatic glands, but no malignancy was found in prostatic urethra and other areas. The patient was discharged three weeks post-operation and completed on adjuvant chemotherapy consisting of Gemcitabine, and Cisplatin to prevent of relapse. The patient is currently in a good healthy.
    CONCLUSIONS: The occurrence of bladder cancer metastasizing to the prostate without involving the prostatic urethra is uncommon and requires precise diagnostic techniques for accurate tumor classification. Early management is advised to enhance the prognosis for the patient.
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  • 文章类型: Case Reports
    颗粒细胞瘤是一种罕见的,主要是良性的,软组织,神经外胚层肿瘤,最常见于皮肤和周围软组织。迄今为止,尚无PSMA-PET在颗粒细胞肿瘤中的亲和力的出版物。在这个60岁的男性中,对局部中等风险前列腺癌进行PSMA-PET分期,偶然发现PSMA-avid左冈上肌病变,随后被活检证实为颗粒细胞瘤。我们介绍了第一例PSMA狂热的颗粒细胞肿瘤,并增加了越来越多的文献,这些文献记载了前列腺癌以外的良性和恶性病变中的PSMA-PET亲和力。
    Granular cell tumour is a rare, mostly benign, soft tissue, neuroectodermal tumour, most commonly seen in the skin and peripheral soft tissue. There are no publications to date of PSMA-PET avidity in a granular cell tumour. In this 60 year old male, staging PSMA-PET for a localized intermediate risk prostate cancer incidentally identified a PSMA-avid left supraspinatus lesion, which was subsequently biopsy-proven as a granular cell tumour. We present the first case of PSMA-avid granular cell tumour and add to the growing literature documenting PSMA-PET avidity in benign and malignant lesions apart from prostate cancer.
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  • 文章类型: Case Reports
    血清碳水化合物抗原19-9(CA19-9)用于胰腺导管腺癌(PDAC)切除患者的复发监测。该报告描述了男性PDAC幸存者中CA19-9增加与前列腺增生的关系。男性PDAC幸存者中原因不明的CA19-9升高可能归因于良性前列腺疾病。
    Serum carbohydrate antigen 19-9 (CA19-9) is used for recurrence surveillance in patients with resected pancreatic ductal adenocarcinoma (PDAC). This report describes the association of increasing CA19-9 in a male PDAC survivor with presence of prostatic hyperplasia. Unexplained elevation of CA19-9 in male PDAC survivors might be attributable to benign prostatic conditions.
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  • 文章类型: Journal Article
    前列腺间质瘤,包括前列腺肉瘤和恶性潜能不确定的间质瘤(STUMP),代表了一种非常罕见的前列腺疾病,患病率低于1%。我们提出了一个罕见的病例,涉及一名40多岁的男子被诊断患有STUMP。尽管存在正常的前列腺特异性抗原(PSA)浓度,患者持续排尿困难和肉眼血尿>7个月,导致良性前列腺增生的初步误诊。持续的症状促使进一步调查,磁共振成像(MRI)显示前列腺左侧有可疑病变,最初被认为是恶性的。经直肠前列腺活检证实存在粘液性脂肪肉瘤,没有糖尿病病史,冠心病,或高血压。治疗方法包括机器人辅助腹腔镜前列腺癌根治术,最终导致术后病理明确诊断为STUMP。该病例强调了早期MRI在诊断过程中不可或缺的作用,强调详细的病理检查的必要性,以确定诊断。我们的报告旨在阐明STUMP的诊断挑战和潜在的治疗途径,强调其在前列腺肿瘤的鉴别诊断中的考虑,以提高这种罕见但重要的疾病的临床结果。
    Prostatic stromal tumors, encompassing prostatic sarcoma and stromal tumors of uncertain malignant potential (STUMP), represent an exceedingly rare category of prostatic diseases, with a prevalence of less than 1%. We present a rare case involving a man in his early 40s diagnosed with STUMP. Despite presenting with normal prostate-specific antigen (PSA) concentrations, the patient experienced persistent dysuria and gross hematuria for >7 months, leading to an initial misdiagnosis of benign prostatic hyperplasia. Persistent symptoms prompted further investigation, with magnetic resonance imaging (MRI) revealing a suspicious lesion on the left side of the prostate, initially thought to be malignant. Transrectal prostatic biopsy subsequently confirmed the presence of mucinous liposarcoma, with no medical history of diabetes, coronary heart disease, or hypertension. The treatment approach comprised robot-assisted laparoscopic radical prostatectomy, culminating in a postoperative pathological definitive diagnosis of STUMP. This case underscores the indispensable role of early MRI in the diagnostic process, highlighting the necessity of detailed pathological examination for a conclusive diagnosis. Our report aims to illuminate the diagnostic challenges and potential treatment pathways for STUMP, emphasizing its consideration in the differential diagnosis of prostatic tumors to advance clinical outcomes in this rare but important condition.
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  • 文章类型: Case Reports
    前列腺的腺样囊性/基底细胞癌(ACC/BCC)是一种罕见的组织学类型,具有各种形态特征,尚未建立最佳治疗方法。我们报告了一名63岁的患者,该患者在经尿道切除高级别尿路上皮膀胱肿瘤后六个月抱怨膀胱排空不全和复发性尿路感染。临床特征,直肠指检,血清PSA水平,多参数MRI未提及任何可疑前列腺病变,膀胱镜检查显示膀胱颈肥大,和前列腺尿道中的淡黄色区域。由于这些发现,进行了经尿道切除术,组织病理学分析显示前列腺的ACC/BCC分化差。尽管ACC/BCC与膀胱尿路上皮癌之间没有被证实的相互关系,尿路阻塞症状的出现,膀胱颈肥大,考虑到ACC/BCC的可能性,经尿道电切活检应重新考虑前列腺尿道的宏观变化。
    Adenoid cystic/Basal-cell carcinoma (ACC/BCC) of the prostate is a rare histological type exhibiting various morphological characteristics and an optimal treatment has not yet been established. We report the case of a 63-year-old patient who complained of incomplete bladder emptying and recurrent urinary infection six months after transurethral resection of a high-grade urothelial bladder tumor. The clinical features, digital rectal examination, serum PSA levels, and multiparametric MRI did not refer to any suspicious prostatic lesions and cystoscopy revealed bladder neck hypertrophy, and yellowish zones in the prostatic urethra. Transurethral resection was performed due to these findings and histopathological analysis showed poorly differentiated ACC/BCC of the prostate. Even though there is no proven mutual correlation between ACC/BCC and urothelial bladder cancer, the appearance of obstructive urinary symptoms, bladder-neck hypertrophy, and macroscopic changes in prostatic urethra should be reconsidered for transurethral resection biopsy considering the possibility of ACC/BCC.
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  • 文章类型: Case Reports
    背景:良性前列腺增生是一种普遍的疾病,可能是严重的顽固性血尿的原因,需要侵入性手术治疗。
    方法:我们报告了三例前列腺源性顽固性血尿的高危病例,并通过前列腺动脉栓塞治疗安全有效,结果良好。
    结论:在非手术治疗中,抗凝患者,前列腺动脉栓塞术是治疗良性前列腺增生相关顽固性血尿的一种安全有效的干预措施。
    BACKGROUND: Benign prostatic hyperplasia is a prevalent disease that could be responsible of severe intractable hematuria requiring invasive surgical management.
    METHODS: We report three high-risk cases presented with intractable hematuria of prostatic origin with high medical co-morbidities treated safely and effectively by prostatic artery embolization with favorable outcomes.
    CONCLUSIONS: In non-surgical, anticoagulated patients, prostatic artery embolization represents a safe and effective intervention for the treatment of intractable hematuria related to benign prostatic hyperplasia.
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  • 文章类型: Case Reports
    黑变病,在没有黑素细胞的情况下黑色素的异常沉积,在泌尿生殖道非常罕见。我们报告了一例74岁的男性,有症状的良性前列腺增生。诊断性膀胱尿道镜检查显示膀胱粘膜显着许多扁平,天鹅绒般的,和棕黑色病变。患者接受了膀胱结石,经尿道前列腺切除术,膀胱活检.膀胱活检的显微镜检查显示尿路上皮颗粒,粘膜和固有层组织细胞内的黑色色素沉着;FontanaMasson染色对黑色素呈阳性。经尿道前列腺电切术的显微镜检查显示结节状增生,基质的黑色色素沉着。膀胱和前列腺黑变病的罕见性凸显了进一步研究的必要性,以阐明其临床意义并确保其良性。尽管它很罕见,当在膀胱镜检查中遇到黑色素病变时,应将黑色素沉着保留在鉴别诊断中。
    Melanosis, the aberrant deposition of melanin pigment in the absence of melanocytes, is very rare in the genitourinary tract. We report a case of a 74-year-old male with symptomatic benign prostatic hyperplasia. Diagnostic cystourethroscopy demonstrated bladder mucosa remarkable for numerous flat, velvety, and brown-black lesions. The patient underwent cystolitholapaxy, transurethral resection of the prostate, and bladder biopsy. Microscopic examination of the bladder biopsy demonstrated urothelium with granular, black pigmentation within the mucosa and histiocytes in the lamina propria; a Fontana Masson stain was positive for melanin. Microscopic examination of the transurethral resection of the prostate demonstrated nodular hyperplasia with focal, black pigmentation of the stroma. The rarity of bladder and prostate melanosis highlights the need for further investigation to elucidate its clinical significance and provide assurance of its benignity. Despite its rarity, melanosis should be kept in the differential diagnosis when melanotic lesions are encountered during cystoscopy.
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  • 文章类型: Case Reports
    一名74岁的男子患有会阴疼痛9个月,泌尿症状进行性恶化,包括夜尿症和尿急。转诊时,他的前列腺特异性抗原(PSA)水平为1.48ng/mL。最初,对前列腺炎或精囊炎症进行了鉴别诊断,开了四周的抗生素,后来由于症状无法解决而延长至六周。然后进行前列腺的磁共振成像(MRI)。印象是精囊增大引起的射精管阻塞,没有明显的前列腺癌的证据。前列腺特异性抗原密度(PSAd)为0.04,前列腺成像报告和数据系统(PIRADS)评分为I-II。进行了CT胸部对比检查,以进一步检查CT尿路图中发现的肺结节。发现多个钙化的肺结节,可疑为恶性肿瘤。对其中一个肺结节进行了CT引导活检,组织病理学分析显示粘液腺癌.然后进行经尿道前列腺切除术(TURP)。前列腺手术标本的组织病理学分析显示浸润性粘液腺癌。根据调查结果,诊断为前列腺粘液腺癌,伴有不典型的肺转移,无骨或区域淋巴结受累,T4阶段N0M1a。该患者目前正在接受卡铂的治疗方案,培美曲塞,和Pembrolizumab.
    A 74-year-old man was suffering from nine months of perineal pain and progressive worsening of urinary symptoms including nocturia and urgency. His prostate-specific antigen (PSA) levels were 1.48 ng/mL at the time of referral. Initially, a differential diagnosis of prostatitis or seminal vesicle inflammation was made, and four weeks of antibiotics were prescribed, which were later extended to six weeks due to failure of symptoms to resolve. Magnetic resonance imaging (MRI) of the prostate was then conducted. The impression was that there was ejaculatory duct obstruction caused by enlarged seminal vesicles with no evidence of significant prostate cancer. The prostate-specific antigen density (PSAd) was 0.04, and the prostate imaging reporting and data system (PIRADS) score was I-II. A CT chest with contrast was conducted for further investigation of pulmonary nodules found on the CT urogram. It revealed multiple calcified pulmonary nodules which were suspicious of malignancy. A CT-guided biopsy of one of the pulmonary nodules was taken, and histopathological analysis revealed a mucinous adenocarcinoma. A transurethral resection of the prostate (TURP) was then performed. Histopathological analysis of the prostatic surgical specimen revealed invasive mucinous adenocarcinoma. Based on the findings, a diagnosis of mucinous adenocarcinoma of the prostate with atypical lung metastasis without osseous or regional lymph node involvement was made, stage T4 N0 M1a. The patient is currently on a treatment regimen consisting of carboplatin, pemetrexed, and pembrolizumab.
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