Cherubism: Case Report with Review of Literature
Identifieur interne : 000956 ( Pmc/Curation ); précédent : 000955; suivant : 000957Cherubism: Case Report with Review of Literature
Auteurs : Divya Mehrotra [Inde] ; Abhishek Kesarwani [Inde]Source :
- Journal of Maxillofacial & Oral Surgery [ 0972-8279 ] ; 2011.
Abstract
Cherubism is a rare hereditary fibro-osseous lesion characterized by painless expansion of jaws in childhood and is known to regress without treatment after puberty. Wait and watch approach has been advocated by many authors. The disease starts early in life manifesting itself fully in the second decade of life and is almost regressed in the third decade. Here, we report two cases of cherubism with clinico-radiographic presentation of its classical features in their third and fourth decade of life respectively and review the literature.
Url:
DOI: 10.1007/s12663-010-0164-y
PubMed: 22379324
PubMed Central: 3177504
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Divya Mehrotra<affiliation><nlm:aff id="Aff2">Kailash Kunj, 4/207, Vivek Khand, Gomtinagar, Lucknow, 226010 Uttar Pradesh India</nlm:aff>
<wicri:noCountry code="subfield">226010 Uttar Pradesh India</wicri:noCountry>
</affiliation>
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<series><title level="j">Journal of Maxillofacial & Oral Surgery</title>
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<front><div type="abstract" xml:lang="en"><p>Cherubism is a rare hereditary fibro-osseous lesion characterized by painless expansion of jaws in childhood and is known to regress without treatment after puberty. Wait and watch approach has been advocated by many authors. The disease starts early in life manifesting itself fully in the second decade of life and is almost regressed in the third decade. Here, we report two cases of cherubism with clinico-radiographic presentation of its classical features in their third and fourth decade of life respectively and review the literature.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Maxillofac Oral Surg</journal-id>
<journal-title-group><journal-title>Journal of Maxillofacial & Oral Surgery</journal-title>
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<issn pub-type="ppub">0972-8279</issn>
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<article-id pub-id-type="doi">10.1007/s12663-010-0164-y</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
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<title-group><article-title>Cherubism: Case Report with Review of Literature</article-title>
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<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Mehrotra</surname>
<given-names>Divya</given-names>
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<address><phone>+91-522-2393841</phone>
<fax>+91-522-4005152</fax>
<email>divyamehrotra@hotmail.com</email>
<email>divyamehrotra2000@yahoo.com</email>
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<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
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<contrib contrib-type="author"><name><surname>Kesarwani</surname>
<given-names>Abhishek</given-names>
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<xref ref-type="aff" rid="Aff1">1</xref>
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<contrib contrib-type="author"><name><surname>Nandlal</surname>
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<xref ref-type="aff" rid="Aff3">3</xref>
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<aff id="Aff1"><label>1</label>
Department of Oral and Maxillofacial Surgery, CSMMU, Formerly King George’s Medical University, Lucknow, India</aff>
<aff id="Aff2"><label>2</label>
Kailash Kunj, 4/207, Vivek Khand, Gomtinagar, Lucknow, 226010 Uttar Pradesh India</aff>
<aff id="Aff3"><label>3</label>
Department of Periodontics, CSMMU, Formerly King George’s Medical University, Lucknow, India</aff>
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<pub-date pub-type="epub"><day>22</day>
<month>3</month>
<year>2011</year>
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<pub-date pub-type="ppub"><month>3</month>
<year>2011</year>
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<volume>10</volume>
<issue>1</issue>
<fpage>64</fpage>
<lpage>70</lpage>
<history><date date-type="received"><day>13</day>
<month>12</month>
<year>2007</year>
</date>
<date date-type="accepted"><day>28</day>
<month>12</month>
<year>2010</year>
</date>
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<permissions><copyright-statement>© Association of Oral and Maxillofacial Surgeons of India 2011</copyright-statement>
</permissions>
<abstract id="Abs1"><p>Cherubism is a rare hereditary fibro-osseous lesion characterized by painless expansion of jaws in childhood and is known to regress without treatment after puberty. Wait and watch approach has been advocated by many authors. The disease starts early in life manifesting itself fully in the second decade of life and is almost regressed in the third decade. Here, we report two cases of cherubism with clinico-radiographic presentation of its classical features in their third and fourth decade of life respectively and review the literature.</p>
</abstract>
<kwd-group><title>Keyword</title>
<kwd>Cherubism</kwd>
<kwd>Fibro osseous</kwd>
<kwd>Maxillary lesion</kwd>
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<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Association of Oral and Maxillofacial Surgeons of India 2011</meta-value>
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