Maxillofacial Mazabraud's syndrome: A case report & review
Author
dc.contributor.author
Domancic, S.
Author
dc.contributor.author
Pezoa, N.
Author
dc.contributor.author
Fernandez-Toro, M.
Author
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Ortega-Pinto, A.
Author
dc.contributor.author
Donoso-Hofer, F.
Admission date
dc.date.accessioned
2018-12-20T15:22:42Z
Available date
dc.date.available
2018-12-20T15:22:42Z
Publication date
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2018
Cita de ítem
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Journal of Stomatology, Oral and Maxillofacial Surgery, Volumen 119, Issue 1, 2018, Pages 44-48.
Identifier
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24687855
Identifier
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10.1016/j.jormas.2017.10.002
Identifier
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https://repositorio.uchile.cl/handle/2250/158973
Abstract
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Mazabraud’s syndrome is characterized by myxomas of intramuscular type present in association with
fibrous dysplasia. Up to this day, approximately 80 cases of Mazabraud’s syndrome have been reported,
although in the head and neck territory intramuscular myxoma reports in association with fibrous
dysplasia of the bone are very scarce. An unusual case of Mazabraud’s syndrome in a 63 years old female
displaying fibrous dysplasia ofthe mandible and softtissue myxoma in the edentulous alveolar ridge in the
molar area is reported.After four years offollow-up,the clinical, imagenological and microscopicalfindings
thatled to the diagnosis and treatment are discussed. This report exemplifies the diagnostic and treatment
challenge of this rare disease and enhances our clinical knowledge due to its long follow-up, highlighting
the need of understanding better its behavior in order to establish proper guidelines for its treatment.