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Oral manifestations of McCune-Albright syndrome

McCune- Albright Syndrome (MAS) is a rare fibrosseous lesion, characterized by a classic triad of polyostotic fibrous dysplasia (PFD), café –au-lait macules (CALM) and underlying endocrinopathies. We present the oral findings of an interesting case of MAS with relevant review of literature. A 30-yea...

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Autores principales: Aravinda, Konidena, Ratnakar, Pamula, Srinivas, Kandakurti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659890/
https://www.ncbi.nlm.nih.gov/pubmed/23776876
http://dx.doi.org/10.4103/2230-8210.107878
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author Aravinda, Konidena
Ratnakar, Pamula
Srinivas, Kandakurti
author_facet Aravinda, Konidena
Ratnakar, Pamula
Srinivas, Kandakurti
author_sort Aravinda, Konidena
collection PubMed
description McCune- Albright Syndrome (MAS) is a rare fibrosseous lesion, characterized by a classic triad of polyostotic fibrous dysplasia (PFD), café –au-lait macules (CALM) and underlying endocrinopathies. We present the oral findings of an interesting case of MAS with relevant review of literature. A 30-year-old male presented to us with swelling of both jaws over a period of two years. Cutaneous examination revealed café - au – lait macule over the back, crossing the midline. Skeletal survey showed expansile, osteolytic, mixed radiolucent- radiopaque lesions in skull and jaw bones. Serum alkaline phosphatase was elevated (388 IU/L), with normal calcium, phosphorus, parathyroid hormone and 25 hydroxy vitamin D levels. Diagnosis of McCune- Albright syndrome was made and he was treated with parenteral bisphosphonates (intravenous Zoledronate 4 mg) and is under follow up for surgical recontouring of the jaws. Early recognition facilitates better treatment and improves prognosis by reducing the morbidity.
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spelling pubmed-36598902013-06-17 Oral manifestations of McCune-Albright syndrome Aravinda, Konidena Ratnakar, Pamula Srinivas, Kandakurti Indian J Endocrinol Metab Case Report McCune- Albright Syndrome (MAS) is a rare fibrosseous lesion, characterized by a classic triad of polyostotic fibrous dysplasia (PFD), café –au-lait macules (CALM) and underlying endocrinopathies. We present the oral findings of an interesting case of MAS with relevant review of literature. A 30-year-old male presented to us with swelling of both jaws over a period of two years. Cutaneous examination revealed café - au – lait macule over the back, crossing the midline. Skeletal survey showed expansile, osteolytic, mixed radiolucent- radiopaque lesions in skull and jaw bones. Serum alkaline phosphatase was elevated (388 IU/L), with normal calcium, phosphorus, parathyroid hormone and 25 hydroxy vitamin D levels. Diagnosis of McCune- Albright syndrome was made and he was treated with parenteral bisphosphonates (intravenous Zoledronate 4 mg) and is under follow up for surgical recontouring of the jaws. Early recognition facilitates better treatment and improves prognosis by reducing the morbidity. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3659890/ /pubmed/23776876 http://dx.doi.org/10.4103/2230-8210.107878 Text en Copyright: © Indian Journal of Endocrinology and Metabolism 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
Aravinda, Konidena
Ratnakar, Pamula
Srinivas, Kandakurti
Oral manifestations of McCune-Albright syndrome
title Oral manifestations of McCune-Albright syndrome
title_full Oral manifestations of McCune-Albright syndrome
title_fullStr Oral manifestations of McCune-Albright syndrome
title_full_unstemmed Oral manifestations of McCune-Albright syndrome
title_short Oral manifestations of McCune-Albright syndrome
title_sort oral manifestations of mccune-albright syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659890/
https://www.ncbi.nlm.nih.gov/pubmed/23776876
http://dx.doi.org/10.4103/2230-8210.107878
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