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Cherubism: Case Report with Review of Literature

Identifieur interne : 000956 ( Pmc/Corpus ); précédent : 000955; suivant : 000957

Cherubism: Case Report with Review of Literature

Auteurs : Divya Mehrotra ; Abhishek Kesarwani

Source :

Journal of Maxillofacial & Oral Surgery [ 0972-8279 ] ; 2011.

RBID : PMC:3177504

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:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177504

DOI: 10.1007/s12663-010-0164-y
PubMed: 22379324
PubMed Central: 3177504

Links to Exploration step

PMC:3177504

Le document en format XML

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<author><name sortKey="Mehrotra, Divya" sort="Mehrotra, Divya" uniqKey="Mehrotra D" first="Divya" last="Mehrotra">Divya Mehrotra</name>
<affiliation><nlm:aff id="Aff1">Department of Oral and Maxillofacial Surgery, CSMMU, Formerly King George’s Medical University, Lucknow, India</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="Aff2">Kailash Kunj, 4/207, Vivek Khand, Gomtinagar, Lucknow, 226010 Uttar Pradesh India</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Kesarwani, Abhishek" sort="Kesarwani, Abhishek" uniqKey="Kesarwani A" first="Abhishek" last="Kesarwani">Abhishek Kesarwani</name>
<affiliation><nlm:aff id="Aff1">Department of Oral and Maxillofacial Surgery, CSMMU, Formerly King George’s Medical University, Lucknow, India</nlm:aff>
</affiliation>
</author>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Cherubism: Case Report with Review of Literature</title>
<author><name sortKey="Mehrotra, Divya" sort="Mehrotra, Divya" uniqKey="Mehrotra D" first="Divya" last="Mehrotra">Divya Mehrotra</name>
<affiliation><nlm:aff id="Aff1">Department of Oral and Maxillofacial Surgery, CSMMU, Formerly King George’s Medical University, Lucknow, India</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="Aff2">Kailash Kunj, 4/207, Vivek Khand, Gomtinagar, Lucknow, 226010 Uttar Pradesh India</nlm:aff>
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</author>
<author><name sortKey="Kesarwani, Abhishek" sort="Kesarwani, Abhishek" uniqKey="Kesarwani A" first="Abhishek" last="Kesarwani">Abhishek Kesarwani</name>
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<series><title level="j">Journal of Maxillofacial & Oral Surgery</title>
<idno type="ISSN">0972-8279</idno>
<idno type="eISSN">0974-942X</idno>
<imprint><date when="2011">2011</date>
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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>
</div>
</front>
</TEI>
<pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
  <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>
</journal-title-group>
<issn pub-type="ppub">0972-8279</issn>
<issn pub-type="epub">0974-942X</issn>
<publisher><publisher-name>Springer-Verlag</publisher-name>
<publisher-loc>India</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">22379324</article-id>
<article-id pub-id-type="pmc">3177504</article-id>
<article-id pub-id-type="publisher-id">164</article-id>
<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>
</subj-group>
</article-categories>
<title-group><article-title>Cherubism: Case Report with Review of Literature</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Mehrotra</surname>
<given-names>Divya</given-names>
</name>
<address><phone>+91-522-2393841</phone>
<fax>+91-522-4005152</fax>
<email>divyamehrotra@hotmail.com</email>
<email>divyamehrotra2000@yahoo.com</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kesarwani</surname>
<given-names>Abhishek</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Nandlal</surname>
</name>
<xref ref-type="aff" rid="Aff3">3</xref>
</contrib>
<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>
</contrib-group>
<pub-date pub-type="epub"><day>22</day>
<month>3</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="ppub"><month>3</month>
<year>2011</year>
</pub-date>
<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>
</history>
<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>
</kwd-group>
<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>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
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Cherubism: Case Report with Review of Literature

Cherubism: Case Report with Review of Literature

Source :

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki