Leiomyosarcoma of the spermatic cord

T. Terada
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Abstract

Leiomyosarcoma of spermatic cord is very rare. The patient is 65-year-old man who presented with a tumor in scrotum. Excision of tumor was performed and it showed a solid tumor measuring 4 cm × 3 cm × 3 cm in left spermatic cord. Histologically, it showed proliferation of hypercellular atypical spindle cells with hyperchromatic nuclei. The tumor cells were arranged with fascicles of cigar-shaped spindled cells with scant acidophilic cytoplasm. The tumor was not encapsulated, and mild invasive features into surrounding tissue were noted. The mitotic index was 17; 17 mitotic figures were seen in 10 high-power-fields. Atypical mitosis was also seen. Immunohistochemically, tumor cells were positive for vimentin, α-smooth muscle actin, h-caldesmon,desmin (focal), p53, and Ki-67 (labeling index = 34%). No other tumors were identified in the body, and the patient further treated with auxiliary local radiation and chemotherapy (cisplatin and doxorubicin). He is now healthy and free from tumors in the body 15 months after the operation.
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精索平滑肌肉瘤
精索平滑肌肉瘤非常罕见。患者为65岁男性,阴囊肿瘤。行肿瘤切除术,左侧精索见一个4 cm × 3 cm × 3 cm的实体瘤。组织学上表现为细胞核深染的非典型梭形细胞增生。肿瘤细胞呈雪茄状梭形细胞束状排列,胞质嗜酸性不足。肿瘤未被包裹,并有轻微侵入周围组织的特征。有丝分裂指数为17;10个高倍视场17个有丝分裂象。非典型有丝分裂也可见。免疫组化结果显示,肿瘤细胞vimentin、α-平滑肌肌动蛋白、h-caldesmon、desmin(局灶)、p53、Ki-67阳性(标记指数34%)。体内未发现其他肿瘤,患者进一步接受辅助局部放化疗(顺铂和阿霉素)。手术15个月后,他现在很健康,体内没有肿瘤。
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