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Primary paratesticular osteosarcoma: case report and a review of the literature.

机译:原发性睾丸旁骨肉瘤:病例报告及文献复习。

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摘要

Primary paratesticular osteosarcoma is an extremely rare malignancy and, to date, only a few cases have been reported. To our knowledge, no such case arising directly from paratesticular soft tissue has been described. We describe a 52-year-old man who presented with left scrotal swelling and an excisional biopsy that revealed a sarcomatous lesion. Left inguinal orchiectomy was performed and histologic examination of the extensively sampled lesion revealed a pure paratesticular osteosarcoma. The patient died 6 months after the diagnosis with disseminated disease.
机译:原发性睾丸旁骨肉瘤是一种极为罕见的恶性肿瘤,迄今为止,仅报道了少数病例。据我们所知,尚未描述直接由睾丸旁软组织引起的这种情况。我们描述了一个52岁的男人,他的左阴囊肿胀和切除的活检显示了肉瘤样病变。进行了左腹股沟睾丸切除术,对广泛取样的病变进行组织学检查,发现其为单纯的睾丸旁骨肉瘤。该患者在诊断为播散性疾病后六个月死亡。

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