Abstract
Ewing’s sarcoma is one of a number of small-roundcell sarcomas that occur in childhood, though its exact origin continues to elude investigators. Pathologically, the best definition is that it is a tumor of small, round, blue cells, usually but not always associated with bone, that lacks markers for lymphoma, neuroblastoma, or rhabdomyosarcoma (Womer 1991). It is not yet clear whether it is a heterogeneous group of tumors that contains subgroups, or a single entity to which several other diagnoses belong. There are two different opinions regarding the origin of Ewing’s sarcoma: that it is of neuroectodermal origin, or that it arises from primitive, undifferentiated, mesenchymal cells (Womer 1991). If the latter is true, the tumor might be better regarded as a blastoma than as a true sarcoma.
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© 1994 Springer-Verlag Berlin Heidelberg
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Marcus, R.B. (1994). Ewing’s Sarcoma. In: Cassady, J.R. (eds) Radiation Therapy in Pediatric Oncology. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84520-8_18
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DOI: https://doi.org/10.1007/978-3-642-84520-8_18
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