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- W2804762389 abstract "Ewing sarcoma (ES) is an aggressive, primary bone malignancy with occasional soft tissue extension. Purely extraosseous 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." @default.
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- W2804762389 date "2018-01-01" @default.
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- W2804762389 title "Primary Spinal Intradural Extraosseous Ewing Sarcoma in a Pediatric Patient: Case Report and Review of the Literature" @default.
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- W2804762389 doi "https://doi.org/10.1159/000488767" @default.
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