Primary Spinal Intradural Extraosseous Ewing Sarcoma in a Pediatric Patient: Case Report and Review of the Literature.

Abstract:

:Ewing sarcoma (ES) is an aggressive, primary bone malignancy with occasional soft tissue extension. Purely extra-osseous ES is rare. A primary intraspinal, intradural ES without bone involvement is exceedingly rare. ES may be differentiated from other primitive neuroectodermal tumors by molecular analysis. The authors report the case of a 14-year-old female who suffered an acute neurologic decline from a hemorrhagic, intraspinal, intradural ES. The patient has been tumor free for 2 years after the initial emergency surgery. Our management of the patient and a review of the literature are provided. Considering only those cases with molecular or genetic confirmation of ES, our patient is the fifth pediatric case reported in the English literature.

journal_name

Pediatr Neurosurg

journal_title

Pediatric neurosurgery

authors

Scantland JT,Gondim MJ,Koivuniemi AS,Fulkerson DH,Shih CS

doi

10.1159/000488767

subject

Has Abstract

pub_date

2018-01-01 00:00:00

pages

222-228

issue

4

eissn

1016-2291

issn

1423-0305

pii

000488767

journal_volume

53

pub_type

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