Ewing's sarcoma and extracranial primitive neuroectodermal tumors
Ewing's sarcoma and extracranial primitive neuroectodermal tumors
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DOI：
10.1097/00001622-199208000-00015
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发表时间：
1992-08
影响因子：
3.4
通讯作者：
L. Granowetter
中科院分区：
文献类型：
--
作者：
L. Granowetter
骨和软组织的尤文氏肉瘤和原始神经外胚层肿瘤是罕见的肿瘤，被认为是儿童的小圆蓝细胞肿瘤。最近的进展联系尤文肉瘤和原始神经外胚层肿瘤，并支持这一概念，这些肿瘤代表分化阶段的肿瘤的神经外胚层起源。化疗的进展导致了大多数患有这些肿瘤的患者的生存。这篇综述简要地概述了今年的文献，关于这种肿瘤的组织发生，生物学和治疗。
Ewing's sarcoma and primitive neuroectodermal tumor of bone and soft tissue are rare tumors, considered with the small round blue cell tumors of childhood. Recent advances link Ewing's sarcoma and primitive neuroectodermal tumor, and support the concept that these tumors represent stages of differentiation in a neoplasm of neuroectodermal origin. Advances in chemotherapy have resulted in the survival of the majority of patients presenting with these tumors. This review briefly outlines the year's literature regarding the histogenesis, biology, and treatment of this tumor.