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    <!-- http://purl.obolibrary.org/obo/MONDO_0017597 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017597">
        <rdfs:label>T-cell/histiocyte rich large B cell lymphoma</rdfs:label>
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        <oboInOwl:hasExactSynonym>T-cell/histiocyte-rich large B-cell lymphoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICDO:9680/3</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>THRLBCL</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C9496</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1321547</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>T-cell rich/histiocyte-rich large B-cell lymphoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICDO:9688/3</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0012257</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MEDGEN:232943</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>T-cell/histiocyte rich large B cell lymphoma (THRLBCL) is a rare variant of diffuse large B-cell lymphoma (DLBCL), mainly affecting middle-aged men and often not being discovered until an advanced disease stage, with involvement of the spleen, liver and bone marrow occurring at a greater frequency than in DLBCL. It is often difficult to diagnose due to its similarity with other lymphoid diseases such as classic Hodgkin lymphoma and nodular lymphocyte-predominant Hodgkin lymphoma and has an aggressive clinical course.</ns3:IAO_0000115>
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