A Rare Case of Paratesticular Leiomyosarcoma

S. Daoudi, I. Adrif, M. Mokrim, H. Mrabti, H. Errihani
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Abstract

: INTRODUCTION: Para testicular leiomyosarcoma is very rare and standard treatment consists of radical orchiectomy and high cord ligation . The tumor usually presents with a painless, slow-growing scrotal mass in middle-aged or older men. 55 year old male patient with painless swelling in right side of scrotum since 4 months. Physical examination revealed a non -tender, solid mass on the right hemi-scrotum, measuring 15x5x3cms in diameter. Ultrasonogram of the scrotum opined right extratesticular mass. High inguinal orchidectomy done. Testis was appearing normal The pathological diagnosis was compatible with a paratesticular leiomyosarcoma Testicular parenchyma was normal with no significant pathology . On immunohistochemical staining, expression of SMA, muscle specific actin, and desmin was observed, while expression of CD34, S-100 protein, vimentin has been negative which confirms the diagnosis of leiomyosarcoma. CONCLUSION: The importance of presenting this paper is because of the rarity of the case and its confirmation by histopathology. oval
睾丸旁平滑肌肉瘤1例
摘要:睾丸旁平滑肌肉瘤非常罕见,标准治疗包括根治性睾丸切除术和高位脐带结扎。中老年男性的肿瘤通常表现为无痛、生长缓慢的阴囊肿块。男性,55岁,右侧阴囊无痛性肿胀4个月。体格检查显示右半阴囊有一无压痛性实性肿块,直径15x5x3cms。阴囊超声图显示右侧睾丸外肿块。完成高腹股沟睾丸切除术。病理诊断符合睾丸旁平滑肌肉瘤,睾丸实质正常,无明显病理变化。免疫组化染色观察到SMA、肌肉特异性肌动蛋白、desmin的表达,CD34、S-100蛋白、vimentin的表达均为阴性,证实了平滑肌肉瘤的诊断。结论:本病例罕见且经组织病理学证实,因此本文具有重要意义。椭圆形
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