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首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >A rare association between malignant mediastinal seminoma and other malignant neoplasms.
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A rare association between malignant mediastinal seminoma and other malignant neoplasms.

机译:恶性纵隔精原细胞瘤与其他恶性肿瘤之间的罕见关联。

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摘要

Primary malignant mediastinal seminomas (PMMS) are rare tumors accounting for 1-6% of all mediastinal tumors. PMMS mostly affect young men, arising from primordial germ cells that abnormally migrate from the ectoderm of the yolk sac to the gonadal region. They are clinically and biologically distinct from primary testicular tumors and seem to have a worse prognosis. Due to the rarity of the disease, the choice of treatment is a matter of debate. Literature data do not show any association between this kind of tumor and malignant Schwannoma or thyroid carcinoma. In this report we describe the case of a patient affected by PMMS and 12 yr later by a malignant brachial plexus Schwannoma and papillary thyroid carcinoma (PTC). Since both mediastinal seminoma and Schwannoma were treated with surgery followed by local radiotherapy, we were not able to ascertain if either PTC or Schwannoma had been induced by radiotherapy or represented a casual neoplastic association.
机译:原发性恶性纵隔精原细胞瘤(PMMS)是罕见的肿瘤,占所有纵隔肿瘤的1-6%。 PMMS主要影响年轻人,这是由于原始生殖细胞异常地从卵黄囊外胚层迁移到性腺区域而引起的。它们在临床和生物学上与原发性睾丸肿瘤不同,并且预后似乎较差。由于该疾病的罕见性,治疗的选择尚有争议。文献数据未显示这种肿瘤与恶性神经鞘瘤或甲状腺癌之间有任何关联。在本报告中,我们描述了一名患者,该患者受PMMS影响,并在12年后受恶性肱神经丛神经鞘瘤和甲状腺乳头状癌(PTC)的影响。由于纵隔精原细胞瘤和神经鞘瘤均接受手术治疗,然后进行局部放疗,因此我们无法确定PTC或神经鞘瘤是通过放疗诱导还是代表偶然的肿瘤形成。

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