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First two cases of craniomaxillofacial fibrous dysplasia from Nepal – case series

Authors Mishra N, Rout SK

Received 28 June 2018

Accepted for publication 11 October 2018

Published 26 November 2018 Volume 2018:10 Pages 269—274

DOI https://doi.org/10.2147/CCIDE.S178599

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Andrew Yee

Peer reviewer comments 2

Editor who approved publication: Dr Christopher Okunseri


Neha Mishra,1 Sourav Kumar Rout2

1Department of Oral and Maxillofacial Pathology and Microbiology, Chitwan Medical College and Teaching Hospital, Bharatpur-10, Chitwan, Nepal; 2Department of Oral and Maxillofacial Surgery, Chitwan Medical College and Teaching Hospital, Bharatpur-10, Chitwan, Nepal

Abstract: Fibrous dysplasia is a benign fibro-osseous disease of the bone, which is most commonly associated with congenital mutations in cAMP regulating protein Gsα coded by GNAS-1 gene. Often it is seen involving the craniofacial skeleton and can range from an asymptomatic monostotic form to polyostotic variant involving almost all the bones of the skull, thereby leading to functional and esthetic problems. This requires a continuous monitoring of the involved region throughout the life of the patient, even after the surgical interventions. We are presenting two cases of craniofacial form of fibrous dysplasia. One case shows monostotic form, while the other case shows features of polyostotic form of disease. To the best of our knowledge, these are the first two cases of craniomaxillofacial fibrous dysplasia from Nepal, which will be reported and published.

Keywords: monostotic, polyostotic, Jaffe–Lichtenstein syndrome, McCune–Albright syndrome, fibro-osseous

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