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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2013
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pubmed-36598902013-06-17 Oral manifestations of McCune-Albright syndrome Aravinda, Konidena Ratnakar, Pamula Srinivas, Kandakurti 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. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Aravinda, Konidena Ratnakar, Pamula Srinivas, Kandakurti |
spellingShingle |
Aravinda, Konidena Ratnakar, Pamula Srinivas, Kandakurti Oral manifestations of McCune-Albright syndrome |
author_facet |
Aravinda, Konidena Ratnakar, Pamula Srinivas, Kandakurti |
author_sort |
Aravinda, Konidena |
title |
Oral manifestations of McCune-Albright syndrome |
title_short |
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_sort |
oral manifestations of mccune-albright syndrome |
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. |
publisher |
Medknow Publications & Media Pvt Ltd |
publishDate |
2013 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659890/ |
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1611979703621517312 |