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首页> 外文期刊>Archives of Medicine and Health Sciences >A rare case of primary mediastinal yolk sac tumor
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A rare case of primary mediastinal yolk sac tumor

机译:罕见的原发性纵隔卵黄囊肿瘤

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Yolk sac tumor (endodermal sinus tumor) is a subtype of germ cell tumor and a highly malignant neoplasm. In addition to presenting in ovaries and testes, the tumor has been detected at several extragonadal sites, including the presacral area, the anterior mediastinum, face, uvula, and the pineal gland. Primary yolk sac tumor of the anterior mediastinum is rare and carries a grave prognosis, affecting mainly young men. Patients often present with advanced, bulky tumors that are unresectable. We present a 16-years-old young male patient with primary yolk sac tumor of mediastinum.
机译:卵黄囊肿瘤(真皮内窦肿瘤)是生殖细胞肿瘤的一种亚型,是高度恶性的肿瘤。除了出现在卵巢和睾丸外,还在几个性腺外部位(包括tumor前区,前纵隔,面部,悬雍垂和松果体)检出了肿瘤。前纵隔的原发性卵黄囊肿瘤很少见,预后严重,主要影响年轻人。患者常表现为不可切除的晚期大块肿瘤。我们介绍了一名患有纵隔原发性卵黄囊瘤的16岁年轻男性患者。

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