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Fibrous dysplasia belongs to a group of fibro-osseous lesions in which cellular fibrous connective tissue stroma replaces bone. It is a developmental hamartomatous lesion with cases occurring below the age of puberty. Fibrous dysplasia can occur as the monostotic form in which single bone is affected and polyostoticwhere multiple bones are involved. Majority of the cases reported are the monostotic form with the common site of involvement being the craniofacial skeleton. Polyostotic form are often associated with McCune-Albright syndrome, Jaffe-Lichtenstein syndrome and, Mazabraud syndrome. The syndromic lesions manifest as atriad of symptoms -fibrous dysplasias, endocrine abnormalities (endocrinopathies like precocious puberty and hypophosphatemia) and skin pigmentations (a cafe-au-lait spots). Fibrous dysplasias are expansile lesions and cause complications associated with the site of origin. The maxilla is the most common site of involvement in the craniofacial skeleton. In this case, a 13-year-old male patient presented who was having maxillary fibrous dysplasia.
Dr. C N V Akhila, Dr. Y. Raghavendra Reddy, Dr. A. Ravi Prakash, Dr. M. Rajinikanth, vikasreddybds. 2019. "Monostotic Fibrous Dysplasia of Maxilla – A Case Report and Review". Global Journal of Medical Research - J: Dentistry & Otolaryngology GJMR-J Volume 19 (GJMR Volume 19 Issue J3).
Crossref Journal DOI 10.17406/gjmr
Print ISSN 0975-5888
e-ISSN 2249-4618
v1.2
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Total Score: 170
Country: India
Subject: Global Journal of Medical Research
Authors: Dr. Y. Raghavendra Reddy, Dr. C.N.V. Akhila, Dr. A. Ravi Prakash, Dr. M. Rajinikanth, Dr.Vikas Reddy (PhD/Dr. count: 5)
View Count (all-time): 452
Total Views (Real + Logic): 771
Total Downloads (simulated): 37
Publish Date: 2019 01, Tue
Monthly Totals (Real + Logic):
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