Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/58280
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dc.contributor.authorRahman, A.-
dc.contributor.authorMadge, S.-
dc.contributor.authorBilling, K.-
dc.contributor.authorAnderson, P.-
dc.contributor.authorLeibovitch, I.-
dc.contributor.authorSelva-Nayagam, D.-
dc.contributor.authorDavid, D.-
dc.date.issued2009-
dc.identifier.citationEye, 2009; 23(12):2175-2181-
dc.identifier.issn0950-222X-
dc.identifier.issn1476-5454-
dc.identifier.urihttp://hdl.handle.net/2440/58280-
dc.description.abstractAim: To present the clinical features and management outcomes in a large longitudinal series of patients with craniofacial fibrous dysplasia (CFD). Methods: Retrospective interventional consecutive case series. Main outcome measures included signs and symptoms, radiographic findings, long-term outcomes, and postoperative complications. Results: A total of 42 patients with CFD were identified. The mean age at presentation was 16.7 years; mean follow-up was 12.6 years. Out of these 42 patients, 37 (88.1%) had unilateral involvement and 5 (11.9%) had bilateral involvement, of which 3 (7.1%) had McCune–Albright syndrome. The commonest presenting symptom was facial asymmetry (36 cases, 86%). The frontal bone was the most commonly involved (27 cases, 64.3%), zfollowed by the sphenoid (24 cases, 57.1%). The most common pattern of bone involvement was monostotic (32 cases, 76.2%). Radiological optic canal involvement occurred in 18 eyes of 15 (37.5%) patients, with optic atrophy in 9 eyes (18.8%) of 7 patients (16.7%). Surgical intervention was performed in 30 (71.4%) cases for both functional and reconstructive reasons. Optic canal decompression was performed in three cases, in all of which stabilization of vision was achieved; no patient lost vision as a result of surgery. Conclusions: In this large longitudinal series of CFD, visual loss was not uncommon and occurred insidiously. The presenting clinical and radiological features, surgical interventions, and outcomes are discussed.-
dc.description.statementofresponsibilityAMA Rahman, SN Madge, K Billing, PJ Anderson, I Leibovitch, D Selva and D David-
dc.description.urihttp://www.nature.com/eye/journal/v23/n12/abs/eye20096a.html-
dc.language.isoen-
dc.publisherNature Publishing Group-
dc.rights© 2009 Macmillan Publishers Limited. All rights reserved-
dc.subjectfibrous dysplasia-
dc.subjectoptic neuropathy-
dc.subjectoptic canal decompression-
dc.titleCraniofacial fibrous dysplasia: clinical characteristics and long-term outcomes-
dc.typeJournal article-
dc.identifier.doi10.1038/eye.2009.6-
pubs.publication-statusPublished-
dc.identifier.orcidAnderson, P. [0000-0002-3730-4652]-
dc.identifier.orcidSelva-Nayagam, D. [0000-0002-2169-5417]-
Appears in Collections:Aurora harvest 5
Opthalmology & Visual Sciences publications

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