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1.
Fogorv Sz ; 103(2): 49-52, 2010 Jun.
Artigo em Húngaro | MEDLINE | ID: mdl-20672752

RESUMO

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.


Assuntos
Dente Canino/diagnóstico por imagem , Maxila , Radiografia Panorâmica , Erupção Dentária , Humanos , Maxila/diagnóstico por imagem , Erupção Ectópica de Dente/diagnóstico por imagem
2.
Fogorv Sz ; 100(2): 65-9, 2007 Apr.
Artigo em Húngaro | MEDLINE | ID: mdl-17546897

RESUMO

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.


Assuntos
Neoplasias Maxilomandibulares/diagnóstico , Neoplasias Maxilomandibulares/cirurgia , Tumores Odontogênicos/diagnóstico , Tumores Odontogênicos/cirurgia , Erupção Ectópica de Dente/etiologia , Dente Impactado/etiologia , Adolescente , Ameloblastoma/diagnóstico , Ameloblastoma/cirurgia , Criança , Feminino , Hamartoma/diagnóstico , Hamartoma/cirurgia , Humanos , Neoplasias Maxilomandibulares/complicações , Neoplasias Maxilomandibulares/diagnóstico por imagem , Neoplasias Maxilomandibulares/patologia , Masculino , Neoplasias Mandibulares/diagnóstico , Neoplasias Mandibulares/cirurgia , Neoplasias Maxilares/diagnóstico , Neoplasias Maxilares/cirurgia , Cistos Odontogênicos/diagnóstico , Cistos Odontogênicos/cirurgia , Tumores Odontogênicos/complicações , Tumores Odontogênicos/diagnóstico por imagem , Tumores Odontogênicos/patologia , Odontoma/diagnóstico , Odontoma/cirurgia , Neoplasias Palatinas/diagnóstico , Neoplasias Palatinas/cirurgia , Radiografia
3.
J Craniomaxillofac Surg ; 35(1): 35-8, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17276078

RESUMO

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.


Assuntos
Cordoma/diagnóstico , Neoplasias da Orelha/diagnóstico , Orelha Externa/patologia , Neoplasias da Base do Crânio/diagnóstico , Neoplasias Encefálicas/diagnóstico , Criança , Cordoma/secundário , Diagnóstico Diferencial , Dor de Orelha/diagnóstico , Face/inervação , Evolução Fatal , Feminino , Humanos , Hipestesia/diagnóstico , Neoplasias Pulmonares/secundário , Doenças Mandibulares/diagnóstico , Mastigação/fisiologia , Invasividade Neoplásica , Lobo Temporal/patologia
4.
Fogorv Sz ; 95(6): 253-6, 2002 Dec.
Artigo em Húngaro | MEDLINE | ID: mdl-12629834

RESUMO

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.


Assuntos
Síndrome de Gardner , Adulto , Feminino , Síndrome de Gardner/diagnóstico por imagem , Síndrome de Gardner/cirurgia , Humanos , Imageamento Tridimensional , Masculino , Tomografia Computadorizada por Raios X
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