Background
This tumor is rare but has an interesting history. For many years, two different tumors, a simple and cellular type, were thought to represent this single tumor. With careful clinical and pathologic examination, it is now clear that the tumor once called simple is now classified as a myxofibroma, a variant of an odontogenic myxoma.
This tumor usually presents as a painless swelling. About 1/3 of cases are associated with the crown of an unerupted tooth. These tumors may displace teeth or resorb the roots of the teeth.
OUTLINE
EPIDEMIOLOGY CHARACTERIZATION INCIDENCE 5% of all odontogenic tumors AGE RANGE-MEDIAN 4-80 years
SEX (M:F)Females 69%
LABORATORY/
RADIOLOGIC/
OTHER TESTSCHARACTERIZATION Radiographs Distinct border, uni to multilocular
12% with calcifications
PROGNOSIS AND TREATMENT CHARACTERIZATION Metastasis None
Recurrence rate is lowTreatment Enucleation with vigorous curettage Sem Diagn Pathol 1999;16:293-296.
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Robbins Pathologic Basis of Disease. Seventh Edition. WB Saunders 2005.
DeMay RM. The Art and Science of Cytopathology. Volume 1 and 2. ASCP Press. 1996.
Weedon D. Weedon's Skin Pathology Second Edition. Churchill Livingstone. 2002
Fitzpatrick's Dermatology in General Medicine. 6th Edition. McGraw-Hill. 2003.
Weiss SW and Goldblum JR. Enzinger and Weiss's Soft Tissue Tumors. Fourth Edition. Mosby 2001.
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