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<oembed><version>1.0</version><provider_name>Revista Brasileira de Oftalmologia</provider_name><provider_url>https://www.rbojournal.org/en/</provider_url><title>Orbital involvement in Rosai-Dorfman disease - Revista Brasileira de Oftalmologia</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="6N0zbGngTK"&gt;&lt;a href="https://www.rbojournal.org/en/article/orbital-involvement-in-rosai-dorfman-disease/"&gt;Orbital involvement in Rosai-Dorfman disease&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.rbojournal.org/en/article/orbital-involvement-in-rosai-dorfman-disease/embed/#?secret=6N0zbGngTK" width="600" height="338" title="&#x201C;Orbital involvement in Rosai-Dorfman disease&#x201D; &#x2014; Revista Brasileira de Oftalmologia" data-secret="6N0zbGngTK" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare idiopathic and benign clinical entity, characterized by histiocytic proliferation with linfofagocitosis. It usually presents with cervical lymphadenopathy although extranodal involvement may occur. The orbital region is one of the most common extranodal sites. It is usually a self-limiting disease with spontaneous resolution but surgical excision, corticosteroids and radiotherapy may be necessary. We describe the case of a 29-years-old male patient complaining of an orbital mass sensation for 6 months [...]</description></oembed>

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