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    <!-- http://purl.obolibrary.org/obo/MONDO_0002531 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002531">
        <rdfs:label>skin neoplasm</rdfs:label>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_1000341 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_1000341">
        <rdfs:label>Lymphomatoid Papulosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002531"/>
        <oboInOwl:hasDbXref>NCIt:C3721</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10056670</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A chronic, recurrent cutaneous disorder characterized by the presence of spontaneously regressing papules. The papules are composed of an atypical lymphocytic infiltrate that contains anaplastic CD30-positive T-cells, which are found in type A and diffuse large cell type (type C) lymphomatoid papulosis. In a small number of cases, of type B, the lymphocytic infiltrate is composed of small, cerebriform-like lymphocytes that are often negative for CD30. The majority of cases follow a benign clinical course, but some cases are clonal and may progress to lymphoma. Treatment options include low dose methotrexate and psoralen/UVA (PUVA).</ns3:IAO_0000115>
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