Craniomaxillofacial fibrous dysplasia: A 10-year database 1996–2006
Autor: | A Kruse, Ch. Zunker, Marc Oliver Riener, Marius Bredell, U. Pieles, K W Grätz |
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Přispěvatelé: | University of Zurich, Kruse, A |
Rok vydání: | 2009 |
Předmět: |
Adult
Male medicine.medical_specialty Adolescent Bone disease 610 Medicine & health Malignant transformation Young Adult Biopsy Foramen Humans Medicine Mandibular Diseases Craniofacial Child Retrospective Studies Foramen magnum medicine.diagnostic_test 3504 Oral Surgery business.industry Fibrous dysplasia Skull Plastic Surgery Procedures medicine.disease Maxillary Diseases 2746 Surgery Surgery Treatment Outcome 2733 Otorhinolaryngology medicine.anatomical_structure Otorhinolaryngology Female 10069 Clinic of Cranio-Maxillofacial Surgery Oral Surgery Tomography X-Ray Computed business Fibrous Dysplasia Monostotic |
Zdroj: | British Journal of Oral and Maxillofacial Surgery. 47:302-305 |
ISSN: | 0266-4356 |
DOI: | 10.1016/j.bjoms.2009.01.008 |
Popis: | Fibrous dysplasia is a rare bone disease caused by an abnormal proliferation of fibrous tissue in bone. We retrospectively evaluated eight patients (female to male ratio 3:1, mean age 22.5 years, range 10-32) with a monostotic form who were treated between 1996 and 2006. Two each were affected in the lower jaw, the upper jaw, the midface, and the frontoparietal region. Most patients were referred because of a painless swelling. Biopsy specimens from two patients were examined, six patients had modelling osteotomies, two of whom had further operations because of progressive enlargement. There was no visual impairment or malignant transformation. Fibrous dysplasia should be treated as conservatively as possible, but in cases of functional disturbance that results from malignant transformation, or from the involvement of the optic foramen or the foramen magnum, an immediate operation is needed. Disfigurement can be another reason for operation. When there is a risk of malignant transformation, follow-up of patients is recommended. |
Databáze: | OpenAIRE |
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