{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T16:34:17Z","timestamp":1787762057317,"version":"build-2784847793"},"reference-count":10,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2023,1]]},"abstract":"Abstract<\/jats:title>\n \n Rationale:<\/jats:title>\n Fibrous dysplasia (FD) is a fibro-osseous lesion of the osseous structures of the body. With an incidence of 1:4000\u20131:10,000, it seems to be a rare disease. Polyostotic craniofacial fibrous dysplasia involves the skull base bones and facial bones.<\/jats:p>\n <\/jats:sec>\n \n Patient Concerns:<\/jats:title>\n The patient complained of a huge swelling over the right side of her face for the past 12 years.<\/jats:p>\n <\/jats:sec>\n \n Diagnosis:<\/jats:title>\n Based on clinical, radiological and histopathological findings, the swelling was diagnosed as polyostotic craniofacial FD.<\/jats:p>\n <\/jats:sec>\n \n Treatment:<\/jats:title>\n Swelling over the right side of the midface around 6 cm \u00d7 5 cm involving right maxilla, zygoma, floor of orbit, lateral side of nose (pyriform aperture) and skull base bones. Since the patient had no functional deficit, we opted for surgical recontouring.<\/jats:p>\n <\/jats:sec>\n \n Outcomes:<\/jats:title>\n The patient was satisfied with post-operative results.<\/jats:p>\n <\/jats:sec>\n \n Take-Away Lessons:<\/jats:title>\n In huge asymptomatic facial deformity, rather than going for resection, we can remove bone in a piecemeal manner followed by recontouring.<\/jats:p>\n <\/jats:sec>","DOI":"10.4103\/ams.ams_33_23","type":"journal-article","created":{"date-parts":[[2023,7,27]],"date-time":"2023-07-27T07:00:42Z","timestamp":1690441242000},"page":"123-126","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["A Massive Craniofacial Polyostotic Fibrous Dysplasia of Midface \u2013 A Rare Case Report"],"prefix":"10.4103","volume":"13","author":[{"given":"Udupi Krishna","family":"Joshi","sequence":"first","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, HKE\u2019s S Nijalingappa Institute of Dental Sciences and Research, Kalaburagi, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Satishkumar G.","family":"Patil","sequence":"additional","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, HKE\u2019s S Nijalingappa Institute of Dental Sciences and Research, Kalaburagi, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sowmya","family":"Thaminidi","sequence":"additional","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, HKE\u2019s S Nijalingappa Institute of Dental Sciences and Research, Kalaburagi, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anand","family":"Mangalgi","sequence":"additional","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, HKE\u2019s S Nijalingappa Institute of Dental Sciences and Research, Kalaburagi, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aaquib","family":"Hashmi","sequence":"additional","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, HKE\u2019s S Nijalingappa Institute of Dental Sciences and Research, Kalaburagi, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2023,7,25]]},"reference":[{"key":"R1-20240828","doi-asserted-by":"crossref","first-page":"788","DOI":"10.1016\/j.jcms.2012.02.016","article-title":"Craniofacial fibrous dysplasia (CFD) of the maxilla in an 11-year old boy: A case report","volume":"40","author":"Assaf","year":"2012","journal-title":"J Craniomaxillofac Surg"},{"key":"R2-20240828","doi-asserted-by":"crossref","first-page":"1966","DOI":"10.1016\/j.joms.2020.05.036","article-title":"Natural history and progression of craniofacial fibrous dysplasia: A retrospective evaluation of 114 patients from Massachusetts general 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Surg"},{"key":"R6-20240828","first-page":"1","article-title":"Monostotic fibrous dysplasia of the mandible in a 9-year-old male patient treated with a conservative surgical treatment: A case report and 15-year follow-up","author":"Berberi","year":"2021","journal-title":"Case Rep Dent 2021"},{"key":"R7-20240828","doi-asserted-by":"crossref","first-page":"485","DOI":"10.32677\/ijcr.v7i11.3108","article-title":"Fibrous dysplasia of maxilla \u2013 A rare case report","volume":"7","author":"Kamble","year":"2021","journal-title":"Indian J Case Rep"},{"key":"R8-20240828","doi-asserted-by":"crossref","first-page":"835","DOI":"10.1097\/00006534-199011000-00002","article-title":"Treatment of craniomaxillofacial fibrous dysplasia: How early and how extensive?","volume":"86","author":"Chen","year":"1990","journal-title":"Plast Reconstr Surg"},{"issue":"4","key":"R9-20240828","article-title":"Use of Weber Ferguson Approach: An Effective Option to Reduce Recurrent Maxillary Fibrous 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