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大细胞神经内分泌前列腺癌的全身转移:一例罕见病例报告及文献综述

Systemic metastases in large cell neuroendocrine prostate cancer: a rare case report and literature review.

作者信息

Xiao Maolin, Tong Wei, Xiao Xiao, Pu Xiaofeng, Yi Faxian

机构信息

Department of Urology, Chongqing General Hospital, Chongqing University, Chongqing, China.

出版信息

Front Oncol. 2024 May 15;14:1398673. doi: 10.3389/fonc.2024.1398673. eCollection 2024.

Abstract

Neuroendocrine prostate neoplasms, encompassing small cell carcinoma, carcinoid, and large cell carcinoma, are infrequently observed in malignant prostate tumors. The occurrence of large cell neuroendocrine prostate cancer (LCNEPC) is exceedingly rare. In this study, the patient initially presented with a persistent dysuria for a duration of one year, accompanied by a serum prostate-specific antigen (PSA) level of 17.83ng/mL. Prostate magnetic resonance imaging (MRI) and chest computed tomography (CT) scan showed that a neoplastic lesion was considered, and prostate biopsy confirmed prostate adenocarcinoma with a Gleason score of 7 (4 + 3). Then, thoracoscopic lung tumor resection was performed, and the pathological examination revealed the presence of primary moderately differentiated invasive adenocarcinoma of the lung and metastatic prostate adenocarcinoma, the Gleason score was 8 (4 + 4). After 1 year of endocrine therapy with goserelin acetate and bicalutamide, he underwent a laparoscopic radical prostatectomy (LRP), the pathological report indicated the presence of adenocarcinoma mixed with NE carcinoma. Two months after the LRP, the patient experienced gross hematuria and sacral tail pain. Further examination revealed multiple metastatic lesions throughout the body. He also underwent transurethral resection of bladder tumor (TURBT) for bladder tumor and received etoposide+ cisplatin chemotherapy three weeks post-surgery. The patient eventually died of multi-organ failure due to myelosuppression after chemotherapy. This case report presents an uncommon instance of LCNEPC with widespread systemic metastases, while also providing a comprehensive review of existing literature to facilitate improved management and treatment strategies for similar patients in subsequent cases.

摘要

神经内分泌前列腺肿瘤,包括小细胞癌、类癌和大细胞癌,在恶性前列腺肿瘤中很少见。大细胞神经内分泌前列腺癌(LCNEPC)的发生极为罕见。在本研究中,患者最初出现持续一年的排尿困难,血清前列腺特异性抗原(PSA)水平为17.83ng/mL。前列腺磁共振成像(MRI)和胸部计算机断层扫描(CT)显示考虑存在肿瘤病变,前列腺活检证实为Gleason评分为7(4+3)的前列腺腺癌。然后,进行了胸腔镜肺肿瘤切除术,病理检查显示存在原发性中度分化浸润性肺腺癌和转移性前列腺腺癌,Gleason评分为8(4+4)。在用醋酸戈舍瑞林和比卡鲁胺进行1年内分泌治疗后,他接受了腹腔镜前列腺癌根治术(LRP),病理报告显示存在腺癌混合神经内分泌癌。LRP术后两个月,患者出现肉眼血尿和骶尾部疼痛。进一步检查发现全身多处转移灶。他还因膀胱肿瘤接受了经尿道膀胱肿瘤切除术(TURBT),并在术后三周接受了依托泊苷+顺铂化疗。患者最终因化疗后骨髓抑制导致多器官衰竭死亡。本病例报告展示了一例罕见的伴有广泛全身转移的LCNEPC病例,同时还对现有文献进行了全面综述,以促进后续类似患者的管理和治疗策略的改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a6b/11133593/911afaa8bd11/fonc-14-1398673-g001.jpg

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