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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">1827</article-id><article-id pub-id-type="doi"/><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>ORBITAL RHABDOMYOSARCOMA -A CASE REPORT&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>G</surname><given-names>Biradar Sunil</given-names></name></contrib><contrib contrib-type="author"><name><surname>M</surname><given-names>Dharmesh Akshatha</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><day>17</day><month>05</month><year>2012</year></pub-date><volume/><issue/><fpage>63</fpage><lpage>66</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>Rhabdomyosarcoma is the most common soft tissue mesenchymal tumour in children. It accounts for 3.4% of all childhood malignancies. Orbital Rhabdomyosarcoma is one the few life threatening disease which, with prompt diagnosis and treatment can be life saving. It can involve the orbit, eye lid, conjunctiva and uveal tract. Following treatment the recurrence rate is reported to be 18 %, metastasis in 6% and death in 3%. A nine year old boy presented with painless progressive eccentric proptosis in Right eye of one month duration. On examination a non tender mass was noted in the inferotemporal region of right orbit, causing upward and inward displacement of the eye ball, suggestive of orbital Rhabdomyosarcoma. Inferior orbitotomy was done and mass was excised in total. Histopathological study confirmed the presence of Rhabdomyosarcoma. Most common site being supero-nasal quadrant, here we report this case due to its atypical site of presentation and under reporting in literature.&#13;
</p></abstract><kwd-group><kwd>Orbital Rhabdomyosarcoma</kwd><kwd> Eccentric proptosis</kwd><kwd> Infero-temporal quadrant</kwd></kwd-group></article-meta></front></article>
