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多原发性肿瘤与神经系统

Multiple primary neoplasms and the nervous system.

作者信息

Schoenberg B S

出版信息

Cancer. 1977 Oct;40(4 Suppl):1961-7. doi: 10.1002/1097-0142(197710)40:4+<1961::aid-cncr2820400831>3.0.co;2-g.

Abstract

Studies of multiple primary neoplasms and their relation to the nervous system should consider two important principles: 1) neoplasms of the nervous system have certain unusual features that distinguish them from tumors occurring elsewhere in the body; and 2) there is good evidence that the various histologic types of nervous system tumors should be regarded as separate diseases. The association of nervous system neoplasms and tumors of other sites may occur in patients with phacomatoses or particular genetic syndromes. In addition, certain nervous system neoplasms may be multicentric in origin. Retinoblastoma and osteosarcoma occur together in the same patient more often than expected by chance, as do meningioma and breast cancer. These relationships are important in that they serve to identify the high risk patient, may provide etiologic clues, may point to the presence of genetic syndromes, and may highlight sites in which subsequent tumors are most likely to develop.

摘要

对多发性原发性肿瘤及其与神经系统关系的研究应考虑两个重要原则

1)神经系统肿瘤具有某些不寻常的特征,使其有别于身体其他部位发生的肿瘤;2)有充分证据表明,神经系统肿瘤的各种组织学类型应被视为独立的疾病。神经系统肿瘤与其他部位肿瘤的关联可能发生在患有错构瘤或特定遗传综合征的患者中。此外,某些神经系统肿瘤可能起源于多中心。视网膜母细胞瘤和骨肉瘤在同一患者中同时出现的频率高于偶然预期,脑膜瘤和乳腺癌也是如此。这些关系很重要,因为它们有助于识别高危患者,可能提供病因线索,可能提示遗传综合征的存在,并可能突出后续肿瘤最有可能发生的部位。

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