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精囊平滑肌肉瘤:病例报告及文献复习。

Seminal vesicle leiomyosarcoma: Case report and literature review.

机构信息

Department of Urology, Hospital Aleman, Buenos Aires, Argentina.

出版信息

Urologia. 2023 Aug;90(3):594-597. doi: 10.1177/03915603211028450. Epub 2021 Jul 25.

Abstract

INTRODUCTION AND BACKGROUND

Primary leiomyosarcoma of the seminal vesicle is an extremely rare and highly malignant disease with less than 15 cases reported.

CASE DESCRIPTION

A 34-year-old man presented with acute urinary symptoms. Imagen studies showed an abdominal mass (80 mm × 65 mm × 50 mm) with contrast enhancement, compressing the right side of the bladder but with a clear cleavage level between surrounding organs. The patient underwent a transrectal US-guided biopsy which was informed as compatible with leiomyosarcoma by immunohistochemical characterization. We performed a cystoprostatectomy and pelvic lymphadenectomy plus radiotherapy. Pathology showed a 7.5 cm × 6 cm nodular para-vesical Leiomyosarcoma histological grade 2 with 0/22 lymph nodes involved. Twelve months after the surgery no recurrences have presented.

CONCLUSION

A multi-disciplinary therapeutic approach, combined with close follow-up, is mandatory to obtain good outcomes in such rare and challenging cases.

摘要

介绍和背景

原发性精囊平滑肌肉瘤是一种极其罕见且高度恶性的疾病,报道病例不足 15 例。

病例描述

一名 34 岁男性出现急性尿路症状。影像学研究显示腹部有一个肿块(80mm×65mm×50mm),增强扫描可见,肿块压迫右侧膀胱,但与周围器官之间有明确的分离平面。患者接受了经直肠超声引导下的活检,免疫组化特征提示符合平滑肌肉瘤。我们进行了膀胱前列腺切除术和盆腔淋巴结清扫术加放疗。病理显示 7.5cm×6cm 结节性副精囊平滑肌肉瘤,组织学分级 2 级,22 个淋巴结无受累。术后 12 个月未出现复发。

结论

对于如此罕见和具有挑战性的病例,需要多学科的治疗方法,并结合密切随访,以获得良好的结果。

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