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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="healthcare" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Radiance Research Academy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">2367</article-id><article-id pub-id-type="doi">10.7324/IJCRR.2017.9225</article-id><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>Healthcare</subject></subj-group></article-categories><title-group><article-title>Juvenile Psammomatoid Ossifying Fibroma - A Rare Entity&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ebenezer</surname><given-names>Evelyn Elizabeth</given-names></name></contrib><contrib contrib-type="author"><name><surname>Harikrishnan</surname><given-names>Volga</given-names></name></contrib><contrib contrib-type="author"><name><surname>Srinivasan</surname><given-names>Chitra</given-names></name></contrib></contrib-group><volume>)</volume><issue/><fpage>22</fpage><lpage>25</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>Aim: Juvenile ossifying fibroma (JOF) is a rare fibro-osseous neoplasm in young children.&#13;
Case Report: 14 year old boy presented with a painless swelling over the palatal region for two months duration which was clinically diagnosed as pyogenic granuloma.&#13;
Discussion: JOF is defined as a variant of the ossifying fibroma, and latter includes juvenile psammomatoid ossifying fibroma (JPOF) and juvenile trabecular ossifying fibroma (JTOF). Both variants involve the craniofacial bones with the trabecular variant being more common in the jaws and the psammomatoid variant being more common in the paranasal sinuses. JPOF may exhibit erosion and invasion of the surrounding bone accompanied by rapid enlargement. JPOF can be distinguished from other maxillofacial fibro osseous lesions by its tendency to recur and its clinical mimicry of malignant bone tumors.&#13;
</p></abstract><kwd-group><kwd>Ossifying fibroma</kwd><kwd> Psammomatoid ossifying fibroma</kwd></kwd-group></article-meta></front></article>
