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    <!-- http://purl.obolibrary.org/obo/MONDO_0021038 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021038">
        <rdfs:label>Ewing sarcoma/peripheral primitive neuroectodermal tumor</rdfs:label>
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        <rdfs:label>extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor</rdfs:label>
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        <ns3:IAO_0000115>A spectrum of malignant tumors arising from the soft tissues, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. Pain and the presence of a mass are the most common clinical symptoms.</ns3:IAO_0000115>
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