Treatment of craniomaxillofacial fibrous dysplasia: How early and how extensive?

Yu Ray Chen*, M. Samuel Noordhoff

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

103 Scopus citations

Abstract

Twenty-eight craniomaxillofacial fibrous dysplasia patients were treated as early as the symptoms occurred. The principles of surgical treatment were based on the zones of involvement: total excision of dysplastic bone of fronto-orbital, zygoma, and upper maxillary origin (zone 1) and bone reconstruction primarily; conservative excision on hair-bearing skull (zone 2), central cranial base (zone 3), and tooth-bearing bones (zone 4); and optic canal decompression on patients with orbital dysplasia and decreasing visual acuity. Patients were followed for 1 to 11 years (average 5.3 years). No recurrence or invasion of the fibrous dysplasia into the grafted bone was seen. One patient had orthognathic maxillary osteotomy on the reconstructed maxilla 6 years after initial reconstruction. Five of 19 patients with alveolar dysplasia had a recurrence and were reshaped. One patient had mandibular sagittal osteotomies to set back the prog-nathic, fibrous dysplasic mandible after three attempts at conservative shaving. Another patient with mandibular fibrous dysplasia had recurrence with pain and a hemi-mandibulectomy with successful immediate free vascular-ized iliac bone graft reconstruction.

Original languageEnglish
Pages (from-to)835-842
Number of pages8
JournalPlastic and Reconstructive Surgery
Volume86
Issue number5
DOIs
StatePublished - 11 1990
Externally publishedYes

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