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Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report

Segmental Odontomaxillary Dysplasia (SOD) is an uncommon, nonhereditary, recently recognized developmental disorder affecting the upper jaw and related dental components. It is a rare condition of uncertain etiology that results in painless unilateral expansion of the posterior dentoalveolar complex...

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Autores principales: Kuklani, Riya M., Nair, Madhu K.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010637/
https://www.ncbi.nlm.nih.gov/pubmed/21197434
http://dx.doi.org/10.1155/2010/837283
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author Kuklani, Riya M.
Nair, Madhu K.
author_facet Kuklani, Riya M.
Nair, Madhu K.
author_sort Kuklani, Riya M.
collection PubMed
description Segmental Odontomaxillary Dysplasia (SOD) is an uncommon, nonhereditary, recently recognized developmental disorder affecting the upper jaw and related dental components. It is a rare condition of uncertain etiology that results in painless unilateral expansion of the posterior dentoalveolar complex, gingival hyperplasia, lack of one or both premolars in the affected area, delayed eruption of adjacent teeth and malformations of the primary molars. Radiographically, the affected bone is thickened and irregular in outline, with coarse trabecular pattern that is vertically oriented resulting in a relatively radiopaque granular appearance. Only a few cases have been reported in the English literature. Considering the rarity of the condition, we report a case of SOD in a pediatric patient who was followed up over a period of over two years. The clinical, radiographic, and histologic features are presented along with a review of the literature.
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spelling pubmed-30106372010-12-30 Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report Kuklani, Riya M. Nair, Madhu K. Int J Dent Case Report Segmental Odontomaxillary Dysplasia (SOD) is an uncommon, nonhereditary, recently recognized developmental disorder affecting the upper jaw and related dental components. It is a rare condition of uncertain etiology that results in painless unilateral expansion of the posterior dentoalveolar complex, gingival hyperplasia, lack of one or both premolars in the affected area, delayed eruption of adjacent teeth and malformations of the primary molars. Radiographically, the affected bone is thickened and irregular in outline, with coarse trabecular pattern that is vertically oriented resulting in a relatively radiopaque granular appearance. Only a few cases have been reported in the English literature. Considering the rarity of the condition, we report a case of SOD in a pediatric patient who was followed up over a period of over two years. The clinical, radiographic, and histologic features are presented along with a review of the literature. Hindawi Publishing Corporation 2010 2010-12-14 /pmc/articles/PMC3010637/ /pubmed/21197434 http://dx.doi.org/10.1155/2010/837283 Text en Copyright © 2010 R. M. Kuklani and M. K. Nair. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kuklani, Riya M.
Nair, Madhu K.
Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title_full Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title_fullStr Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title_full_unstemmed Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title_short Segmental Odontomaxillary Dysplasia: Review of the Literature and Case Report
title_sort segmental odontomaxillary dysplasia: review of the literature and case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010637/
https://www.ncbi.nlm.nih.gov/pubmed/21197434
http://dx.doi.org/10.1155/2010/837283
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