Leiomyosarcoma of lower urinary tract: Literature review.

IF 1.9 Q3 UROLOGY & NEPHROLOGY
Central European Journal of Urology Pub Date : 2025-01-01 Epub Date: 2025-11-27 DOI:10.5173/ceju.2025.0157
Layla Settaf-Cherif, Michał C Czarnogórski, Adam Ostrowski, Wojciech Flis, Maciej Socha, Przemysław Adamczyk, Julia Drewa, Jan Adamowicz, Kajetan Juszczak
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引用次数: 0

Abstract

Introduction: Leiomyosarcoma (LMS) of the lower urinary tract (LUT) is a rare and aggressive malignancy derived from smooth muscle cells. It most commonly arises in the bladder, is less frequent in the prostate, and exceptionally rare in the urethra. The disease typically affects adults around the sixth decade of life with a slight male predominance. Etiology remains unclear, although previous radiotherapy or exposure to specific chemotherapeutic agents has been implicated. Clinical presentation is often nonspecific and may resemble more prevalent urinary tract diseases, contributing to delayed or inaccurate diagnosis.

Material and methods: This narrative review summarizes current knowledge on LUT LMS based on available case reports and small case series. The literature was analyzed with focus on epidemiology, clinical features, diagnostic methods, and treatment strategies to highlight challenges in management and areas requiring further investigation.

Results: Diagnosis of LUT LMS relies on histopathological assessment supported by immunohistochemistry, typically demonstrating positivity for smooth muscle markers such as smooth muscle actin, desmin, h-caldesmon, and vimentin. Surgery remains the cornerstone of treatment. Radical cystectomy is the most common approach for bladder tumors, while prostatic and urethral involvement often necessitates extensive surgical resection. The effectiveness of chemotherapy and radiotherapy is uncertain, and their use is tailored to individual tumor characteristics and patient condition. Regardless of location, prognosis is generally poor due to biological aggressiveness and frequent late presentation.

Conclusions: LUT LMS is an extremely rare malignancy with limited evidence available to guide management. Further research, including multicenter databases and prospective studies, is needed to establish prognostic factors and optimize treatment. Multidisciplinary collaboration is essential to ensure timely diagnosis, appropriate therapeutic planning, and improved patient outcomes.

下尿路平滑肌肉瘤:文献回顾。
简介:下尿路平滑肌肉瘤(LMS)是一种罕见的起源于平滑肌细胞的侵袭性恶性肿瘤。它最常见于膀胱,在前列腺中较少见,在尿道中极为罕见。这种疾病通常发生在60岁左右的成年人身上,男性略占优势。病因尚不清楚,尽管先前的放疗或暴露于特定的化疗药物已被牵连。临床表现通常是非特异性的,可能类似于更普遍的泌尿道疾病,导致延迟或不准确的诊断。材料和方法:本文基于现有病例报告和小病例系列,总结了目前关于LUT LMS的知识。对文献进行分析,重点是流行病学、临床特征、诊断方法和治疗策略,以突出管理方面的挑战和需要进一步研究的领域。结果:LUT LMS的诊断依赖于免疫组织化学支持的组织病理学评估,通常显示平滑肌标记物阳性,如平滑肌肌动蛋白、desmin、h-caldesmon和vimentin。手术仍然是治疗的基石。根治性膀胱切除术是膀胱肿瘤最常见的治疗方法,而累及前列腺和尿道往往需要广泛的手术切除。化疗和放疗的有效性是不确定的,它们的使用是根据个体肿瘤特征和患者的情况量身定制的。无论在哪个部位,由于生物侵袭性和频繁迟发,预后通常较差。结论:LUT LMS是一种极其罕见的恶性肿瘤,指导治疗的证据有限。需要进一步的研究,包括多中心数据库和前瞻性研究,以确定预后因素和优化治疗。多学科合作对于确保及时诊断、适当的治疗计划和改善患者预后至关重要。
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
Central European Journal of Urology
Central European Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
2.30
自引率
8.30%
发文量
48
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