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1.
Fogorv Sz ; 103(2): 49-52, 2010 Jun.
Article in Hungarian | MEDLINE | ID: mdl-20672752

ABSTRACT

Upper canines have significant esthetical and functional roles in the dental arch. Upper canine retention is a frequent anomaly as the germ develops rather far from its final place. Moreover, the neighboring teeth may narrow the place of the canine because of its late eruption. Impacted canines without treatment may cause severe complications. Impaction of canines can be diagnosed early by clinical and radiological findings, which enables the clinician to perform a complete rehabilitation by successful surgical and orthodontic treatment.


Subject(s)
Cuspid/diagnostic imaging , Maxilla , Radiography, Panoramic , Tooth Eruption , Humans , Maxilla/diagnostic imaging , Tooth Eruption, Ectopic/diagnostic imaging
2.
Fogorv Sz ; 100(2): 65-9, 2007 Apr.
Article in Hungarian | MEDLINE | ID: mdl-17546897

ABSTRACT

Mixed odontogenic tumors in the jaws of children and adolescents usually cause dentition anomalies. The typical forms of these are ameloblastic fibroma, ameloblastic fibroodontoma, complex odontoma and compound odontoma. In the present study mixed odontogenic tumor cases are presented in patients under 20 years of age. All of them were associated with tooth eruption disturbances. Further aim of this study was to discuss the nature and interrelationships of this group of lesions. Ameloblastic fibromas (AFs) are true, mixed, soft tissue neoplasms, deriving from the proliferation of both odontogenic epithelium and mesenchyma. They have a potential to both recurrence and malignant transformation. Ameloblastic fibroodontomas (AFOs) may be regarded as hamartomas, which exhibit epithelial, mesenchymal and abundant hard tissue components of the developing teeth. Odontomas are calcifying benign hamartomas, and represent the most common type of odontogenic jaw tumors among patients less than 20y, having complex and compound variants. Complex odontomas (CXOs) are built up from amorphous hard tissue elements, and generally occur in the premolar or molar regions of the maxilla. Compound odontomas (CDOs) usually appear in the maxilla, in the region of the incisors and canines, and contain small, radio-opaque structures reminiscent of rudimentary teeth. Early diagnosis and treatment of mixed odontogenic jaw tumors in children may prevent the serious orthodontic complications and jaw deformations.


Subject(s)
Jaw Neoplasms/diagnosis , Jaw Neoplasms/surgery , Odontogenic Tumors/diagnosis , Odontogenic Tumors/surgery , Tooth Eruption, Ectopic/etiology , Tooth, Impacted/etiology , Adolescent , Ameloblastoma/diagnosis , Ameloblastoma/surgery , Child , Female , Hamartoma/diagnosis , Hamartoma/surgery , Humans , Jaw Neoplasms/complications , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/pathology , Male , Mandibular Neoplasms/diagnosis , Mandibular Neoplasms/surgery , Maxillary Neoplasms/diagnosis , Maxillary Neoplasms/surgery , Odontogenic Cysts/diagnosis , Odontogenic Cysts/surgery , Odontogenic Tumors/complications , Odontogenic Tumors/diagnostic imaging , Odontogenic Tumors/pathology , Odontoma/diagnosis , Odontoma/surgery , Palatal Neoplasms/diagnosis , Palatal Neoplasms/surgery , Radiography
3.
J Craniomaxillofac Surg ; 35(1): 35-8, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17276078

ABSTRACT

INTRODUCTION: The extreme rarity of chordomas in childhood, the slow growing nature of these tumours and the diverse symptoms may cause many diagnostic problems. PATIENT: A 9-year-old girl presented with an unusual manifestation of a skull base chordoma. The clinical and pathological features were analysed. RESULT: In the present case, the initial symptoms of the skull base tumour were completely misleading. The otodynia, the masticatory difficulties and the mass in the preauricular region were not characteristic of skull base chordomas. The female sex, the young age, the large tumour size and the atypical histological pattern of the tumour all indicated a very poor prognosis. CONCLUSION: The rarity of this tumour in childhood and the atypical lateral and intracranial spread resulted in a serious delay of the diagnosis and in a fatal outcome.


Subject(s)
Chordoma/diagnosis , Ear Neoplasms/diagnosis , Ear, External/pathology , Skull Base Neoplasms/diagnosis , Brain Neoplasms/diagnosis , Child , Chordoma/secondary , Diagnosis, Differential , Earache/diagnosis , Face/innervation , Fatal Outcome , Female , Humans , Hypesthesia/diagnosis , Lung Neoplasms/secondary , Mandibular Diseases/diagnosis , Mastication/physiology , Neoplasm Invasiveness , Temporal Lobe/pathology
4.
Fogorv Sz ; 95(6): 253-6, 2002 Dec.
Article in Hungarian | MEDLINE | ID: mdl-12629834

ABSTRACT

The authors discuss 3 cases of Gardner-syndrome, outlining malignized large intestine polyposis, multiplex osteomas and the different skin tumours as the main features. The earliest symptoms suspecting the clinical picture are usually dental and/or mandibular lesions and draw the attention to the highly malignant polyposis.


Subject(s)
Gardner Syndrome , Adult , Female , Gardner Syndrome/diagnostic imaging , Gardner Syndrome/surgery , Humans , Imaging, Three-Dimensional , Male , Tomography, X-Ray Computed
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