Undifferentiated Pleomorphic Sarcoma of the Prostate, a Rare Cause of Genitourinary Tumour in Men.

IF 0.9 4区 医学 Q4 UROLOGY & NEPHROLOGY
Marta Guerra Lacambra, María Teresa Melgarejo Segura, Yaiza Yáñez Castillo, María Eugenia Folgueral Corral, Miguel Arrabal Martín
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Abstract

Background: Undifferentiated pleomorphic sarcoma (UPS) of the prostate is an extremely rare and malignant tumour, accounting for only 0.1%-0.24% of all prostate neoplasms. Reclassified as a malignant fibrous histiocytoma by the World Health Organization in 2002, UPS predominantly affects men aged 50-70 years. Diagnosis is difficult due to nonspecific symptoms, such as acute urinary retention (AUR) and haematuria, along with normal prostate-specific antigen levels, which often lead to confusion with benign prostatic hyperplasia.

Methods: This case report discusses the clinical presentation, diagnostic process and management of an 82-year-old man who presented with AUR. Imaging studies, such as transrectal ultrasound, computed tomography and magnetic resonance imaging, were used to evaluate the tumour. Histological examination and immunostaining were performed after transurethral resection to confirm the diagnosis of UPS.

Results: The images revealed a large, irregular, invasive tumour within the prostate, leading to a radical cystoprostatectomy. Histological analysis showed atypical spindle cells and positive immunostaining for histiocytic markers, such as vimentin and CD68 (a marker of monocyte/macrophage lineage), confirming the diagnosis of UPS. Surgical margins were negative, and no residual disease was detected in the postoperative period.

Conclusions: The rarity of prostatic UPS underscores the ongoing debate about its optimal management. This case contributes to the limited literature on prostatic UPS, highlighting the importance of early detection and complete surgical removal to improve prognosis. More research is needed to establish a consensus on adjuvant therapies.

前列腺未分化多形性肉瘤是男性泌尿生殖系统肿瘤的罕见病因。
背景:前列腺未分化多形性肉瘤(Undifferentiated pleomorphic sarcoma, UPS)是一种极为罕见的恶性肿瘤,仅占所有前列腺肿瘤的0.1%-0.24%。2002年,世界卫生组织将UPS重新归类为恶性纤维组织细胞瘤,主要影响50-70岁的男性。由于非特异性症状,如急性尿潴留(AUR)和血尿,以及正常的前列腺特异性抗原水平,诊断困难,这往往导致与良性前列腺增生混淆。方法:本病例报告讨论了一例82岁男性AUR的临床表现、诊断过程和治疗。影像学研究,如经直肠超声,计算机断层扫描和磁共振成像,用于评估肿瘤。经尿道切除术后行组织学检查和免疫染色以确定UPS的诊断。结果:图像显示一个巨大的,不规则的,侵袭性肿瘤在前列腺内,导致根治性膀胱前列腺切除术。组织学分析显示非典型梭形细胞和组织细胞标记物免疫染色阳性,如vimentin和CD68(单核/巨噬细胞谱系的标记物),证实了UPS的诊断。手术切缘阴性,术后未发现残留病变。结论:前列腺UPS的罕见性强调了关于其最佳治疗的持续争论。该病例增加了关于前列腺UPS的有限文献,强调了早期发现和完全手术切除对改善预后的重要性。需要更多的研究来建立对辅助治疗的共识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archivos Espanoles De Urologia
Archivos Espanoles De Urologia UROLOGY & NEPHROLOGY-
CiteScore
0.90
自引率
0.00%
发文量
111
期刊介绍: Archivos Españoles de Urología published since 1944, is an international peer review, susbscription Journal on Urology with original and review articles on different subjets in Urology: oncology, endourology, laparoscopic, andrology, lithiasis, pediatrics , urodynamics,... Case Report are also admitted.
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