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1.
J Stomatol Oral Maxillofac Surg ; 119(2): 140-144, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29074442

ABSTRACT

Ossifying fibroma (OF) is a benign fibro-osseous lesion mainly occurring in young adults and seems to originate from the periodontal ligament. Aneurysmal bone cyst (ABC) is a benign intraosseous lesion characterized by blood-filled spaces of various sizes. These two lesions can specifically affect the jaws and are commonly described in the literature. However, few cases describing an association of OF and ABC have been reported in the literature, especially in the maxillary sinus. We report the case of a 40-year-old male patient affected with an asymptomatic lesion with a dual component of OF and ABC laying in the maxillary sinus. Our aim is to discuss its clinical and morphological features as well as treatment results.


Subject(s)
Bone Cysts, Aneurysmal , Fibroma, Ossifying , Fistula , Adult , Conservative Treatment , Female , Humans , Male , Maxillary Sinus , Pregnancy , Young Adult
2.
Oral Dis ; 16(3): 292-8, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20374512

ABSTRACT

OBJECTIVE: The aim of this study was to provide a quantification of taurodontism in Hypohidrotic Ectodermal Dysplasia (HED) and to report its occurrence in a cohort of HED patients to assess phenotypic-genotypic correlations. PATIENTS AND METHODS: Of 68 HED patients retrospectively reviewed, 16 patients aged 7-51 years were selected and compared with a control sample (n = 351). The pulp surface index of the first lower permanent molar was calculated from the panoramic radiograph of each individual, and statistical comparisons between the HED patients and the control sample were performed. RESULTS: Whatever the genetic disorder, 81.25% of the HED patients exhibited a relative enlargement (>or=1 s.d.) of the pulp. Major deviations (>5 s.d.) were respectively related to men affected by large deletion of the EDA gene or missense mutation. The autosomal recessive form was linked to a relative moderate pulp enlargement (3.44 s.d.). In NEMO forms, the increase of pulp size in men appeared to be less marked than in EDA mutations. CONCLUSION: This study provides for the first time an objective assessment of pulp enlargement in HED patients, and the various degrees of taurodontism depicted could be interesting dental phenotypic markers of HED forms.


Subject(s)
Dental Pulp Cavity/abnormalities , Ectodermal Dysplasia 1, Anhidrotic/diagnosis , Ectodermal Dysplasia 3, Anhidrotic/diagnosis , Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive/diagnosis , Tooth Abnormalities/genetics , Adolescent , Adult , Case-Control Studies , Child , Child, Preschool , DNA Mutational Analysis , Dental Pulp Cavity/diagnostic imaging , Ectodermal Dysplasia 1, Anhidrotic/complications , Ectodermal Dysplasia 1, Anhidrotic/genetics , Ectodermal Dysplasia 3, Anhidrotic/complications , Ectodermal Dysplasia 3, Anhidrotic/genetics , Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive/complications , Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive/genetics , Ectodysplasins/genetics , Female , Humans , I-kappa B Kinase/genetics , Male , Middle Aged , Molar/abnormalities , Molar/diagnostic imaging , Mutation, Missense , Radiography , Retrospective Studies , Sequence Deletion , Tooth Abnormalities/etiology , Young Adult
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