N	Concordance
1	spread.   Every patient with anaplastic ependymoma should be evaluated with diag
2	would be  referred to as an astrocytoma-ependymoma and would show characteristic
3	ormalities and aneuploidy in  childhood ependymoma. IV.  Assess the feasibility
4	ny location (except primary spinal cord ependymoma), less than 3 years at d
5	 ary ependymoma and well-differentiated ependymoma, and are often curable.     A
6	 neuroectodermal tumor, or disseminated ependymoma treated with preradiation com
7	gery is the first form of treatment for ependymoma. The aim of surgery is to rem
8	r investigational studies are needed in ependymoma and diffuse pontine gliomas b
9	firmed supratentorial or infratentorial ependymoma or anaplastic ependymoma    
10	ve children with localized intracranial ependymoma. Preliminary results in young
11	as   These tumors include myxopapillary ependymoma and well-differentiated  epen
12	ultrastructural findings, four types of ependymoma were classified, namely, the 
13	 Treatment for childhood supratentorial ependymoma may be surgery followed by  r