Parosteal osteochondrolıpoma of the mandıble

Osteochondrolipoma is a rare benign soft tissue neoplasm. It is occasionally considered to be a variant of adipose tissue neoplasm ‘lipoma’ showing multiple differentiation pathways of pluripotent stem cells. As with the lipomas they can be seen at any location and show cartilagenous and osteoid dif...

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Autores principales: Gültekin, Sibel Elif, Kahraman, Sevil, Karadayı, Kıvanç
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424949/
https://www.ncbi.nlm.nih.gov/pubmed/22923905
http://dx.doi.org/10.4103/0973-029X.99090
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author Gültekin, Sibel Elif
Kahraman, Sevil
Karadayı, Kıvanç
author_facet Gültekin, Sibel Elif
Kahraman, Sevil
Karadayı, Kıvanç
author_sort Gültekin, Sibel Elif
collection PubMed
description Osteochondrolipoma is a rare benign soft tissue neoplasm. It is occasionally considered to be a variant of adipose tissue neoplasm ‘lipoma’ showing multiple differentiation pathways of pluripotent stem cells. As with the lipomas they can be seen at any location and show cartilagenous and osteoid differentiation when located parosteally. We present a case of osteochondrolipoma located at the symphysis of the mandible. To our knowledge, this is the first reported case of an oral osteochondrolipoma associated with parosteal localization.
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spelling pubmed-34249492012-08-24 Parosteal osteochondrolıpoma of the mandıble Gültekin, Sibel Elif Kahraman, Sevil Karadayı, Kıvanç J Oral Maxillofac Pathol Case Report Osteochondrolipoma is a rare benign soft tissue neoplasm. It is occasionally considered to be a variant of adipose tissue neoplasm ‘lipoma’ showing multiple differentiation pathways of pluripotent stem cells. As with the lipomas they can be seen at any location and show cartilagenous and osteoid differentiation when located parosteally. We present a case of osteochondrolipoma located at the symphysis of the mandible. To our knowledge, this is the first reported case of an oral osteochondrolipoma associated with parosteal localization. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3424949/ /pubmed/22923905 http://dx.doi.org/10.4103/0973-029X.99090 Text en Copyright: © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gültekin, Sibel Elif
Kahraman, Sevil
Karadayı, Kıvanç
Parosteal osteochondrolıpoma of the mandıble
title Parosteal osteochondrolıpoma of the mandıble
title_full Parosteal osteochondrolıpoma of the mandıble
title_fullStr Parosteal osteochondrolıpoma of the mandıble
title_full_unstemmed Parosteal osteochondrolıpoma of the mandıble
title_short Parosteal osteochondrolıpoma of the mandıble
title_sort parosteal osteochondrolıpoma of the mandıble
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424949/
https://www.ncbi.nlm.nih.gov/pubmed/22923905
http://dx.doi.org/10.4103/0973-029X.99090
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AT kahramansevil parostealosteochondrolıpomaofthemandıble
AT karadayıkıvanc parostealosteochondrolıpomaofthemandıble

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