A non-classic form of McCune Albright syndrome with different presentations and review of the literatures

BACKGROUND: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group. Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine pathways. CASE REPORT: We report the case of an...

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Autores principales: Navabazam, Alireza, Owlia, Fatemeh, Akhavan Karbassi, Mohammad Hassan, Hakimian, Roqayeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559639/
https://www.ncbi.nlm.nih.gov/pubmed/34760092
http://dx.doi.org/10.22088/cjim.12.0.401
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author Navabazam, Alireza
Owlia, Fatemeh
Akhavan Karbassi, Mohammad Hassan
Hakimian, Roqayeh
author_facet Navabazam, Alireza
Owlia, Fatemeh
Akhavan Karbassi, Mohammad Hassan
Hakimian, Roqayeh
author_sort Navabazam, Alireza
collection PubMed
description BACKGROUND: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group. Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine pathways. CASE REPORT: We report the case of an 18-year old girl with non-classic form of MAS .New aspect of this case report attributed to multiple sebaceous adenoma. CONCLUSION: The new finding of our case of MAS was not reported before. Periodic follow-up with different radiologic and laboratory tests should be considered after suspicion to MAS.
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spelling pubmed-85596392021-11-09 A non-classic form of McCune Albright syndrome with different presentations and review of the literatures Navabazam, Alireza Owlia, Fatemeh Akhavan Karbassi, Mohammad Hassan Hakimian, Roqayeh Caspian J Intern Med Case Report BACKGROUND: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group. Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine pathways. CASE REPORT: We report the case of an 18-year old girl with non-classic form of MAS .New aspect of this case report attributed to multiple sebaceous adenoma. CONCLUSION: The new finding of our case of MAS was not reported before. Periodic follow-up with different radiologic and laboratory tests should be considered after suspicion to MAS. Babol University of Medical Sciences 2021 /pmc/articles/PMC8559639/ /pubmed/34760092 http://dx.doi.org/10.22088/cjim.12.0.401 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Navabazam, Alireza
Owlia, Fatemeh
Akhavan Karbassi, Mohammad Hassan
Hakimian, Roqayeh
A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title_full A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title_fullStr A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title_full_unstemmed A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title_short A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
title_sort non-classic form of mccune albright syndrome with different presentations and review of the literatures
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559639/
https://www.ncbi.nlm.nih.gov/pubmed/34760092
http://dx.doi.org/10.22088/cjim.12.0.401
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