Barson A J, Ahmed A, Gibson A A, MacDonald A M
Arch Dis Child. 1978 Nov;53(11):882-9. doi: 10.1136/adc.53.11.882.
Four cases of a locally invasive sarcoma of the chest wall are described in children aged between 8 and 14 years. Although its morphology resembles a Ewing's sarcoma of bone there are light and electron microscopical features that are distinctive. The sarcoma is thought to represent an entity which has not previously been defined. Its clinical importance lies in the fact that the prognosis with appropriate treatment appears to be good. One child died after 2 1/2 years, but the others are alive 6, 8, and 16 years after presentation.
本文描述了4例年龄在8至14岁之间的儿童胸壁局部浸润性肉瘤。尽管其形态学类似于骨尤文肉瘤,但有独特的光镜和电镜特征。这种肉瘤被认为代表一种此前未被定义的实体。其临床重要性在于,经适当治疗后的预后似乎良好。1名儿童在2年半后死亡,但其他儿童在就诊后6年、8年和16年仍存活。