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1.
Med Oral Patol Oral Cir Bucal ; 24(3): e305-e313, 2019 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-31011141

RESUMO

BACKGROUND: To evaluate the frequency of maxillary dentures-related lesions and the possible associated risk factors. MATERIAL AND METHODS: Ninety-seven participants were selected, and a complete anamnesis, physical examination and tests of occlusion vertical dimension (OVD), retention and stability of the denture, biofilm quantification, cytopathology, sialometry, pH analysis and buffer capacity of the saliva were performed. Statistical analyses were performed with the Pearson's chi-square, Mann-Whitney tests, and Pearson's coefficient (p<0.05). RESULTS: In 78% of the participants at least one denture-related lesion was found. Denture-associated stomatitis (63%), inflammatory fibrous hyperplasia (19%) and traumatic ulceration (11%) were the 3 most frequent lesions. The habit of night use of the denture was considered an independent risk factor for the development of oral lesions [OR=3.0 (95% CI 1.09-8.56); p<0.05]. Furthermore, the longest period of use of the same denture and biofilm also had statistically significant relation to oral lesions. The biofilm seems to be more related to the prevalence of oral lesions according to the multiple logistic regression [OR=1.3 (95% CI: 1.01-1.83) p<0.05]. The lack of a dentures' cleaning solution and detrition of the prothesis were independent risk factors for denture-associated stomatitis. Male gender, loss of OVD and bad buffer capacity were risk factors for angular cheilitis. Fractures of the base and repair of broken dentures were risk factors for traumatic ulcers. CONCLUSIONS: These results show a high frequency of denture-related lesions. Besides, participants hygiene habits and poor quality of the dentures were the main factors for the development of these lesions.


Assuntos
Dentaduras , Estomatite sob Prótese , Estudos Transversais , Humanos , Masculino , Maxila , Fatores de Risco
2.
Int J Oral Maxillofac Surg ; 42(4): 432-5, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22749542

RESUMO

The use of injectable cosmetic fillers in orofacial tissues has increased in the past few years. Although a wide variety of agents are available on the market and satisfactory results have been achieved, adverse reactions can be observed. The authors report three new cases of oral reactions in three women who received injections of different cosmetic fillers in the perioral area. In two cases, the lesions presented as nodules on the lip mucosa, and in the last case, as an intraoral ulcer with submental swelling. Considering the concern of patients about malignancies in these lesions, clinicians and pathologists should be aware of these adverse reactions and a detailed history should be made to diagnose these conditions.


Assuntos
Materiais Biocompatíveis/efeitos adversos , Técnicas Cosméticas/efeitos adversos , Reação a Corpo Estranho/etiologia , Mucosa Bucal/patologia , Silicones/efeitos adversos , Adulto , Feminino , Humanos , Ácido Hialurônico/efeitos adversos , Injeções Subcutâneas , Pessoa de Meia-Idade
3.
Oral Dis ; 18(2): 184-90, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22023169

RESUMO

BACKGROUND: Cleidocranial dysplasia (CCD) is a dominantly inherited autosomal disease characterized by typical bone defects including short stature, persistently open or delayed closure of the cranial sutures, and hypoplastic or aplastic clavicles. Oral features are frequent and include supernumerary teeth, delayed eruption or impaction of the permanent teeth, and malocclusion. Heterozygous mutations in RUNX2 gene, which encodes a transcription factor essential for osteoblast differentiation, were identified as the etiological cause of CCD. OBJECTIVE AND METHODS: Herein, we performed physical and radiographic examination and screening for RUNX2 mutations in 11 patients from five families with CCD. RESULTS: All patients demonstrated the classical phenotypes related to CCD. Families whose affected members had several dental alterations such as multiple impacted and supernumerary teeth demonstrated heterozygous missense mutations (R190Q and R225Q) that impair the runt domain of RUNX2. On the other hand, CCD patients from families with low frequency of dental abnormalities showed no mutation in RUNX2 or mutation outside of the runt domain (Q292fs→X299). CONCLUSION: The current findings suggest a correlation between dental alterations and mutations in the runt domain of RUNX2 in CCD patients. Further clinical and genetic studies are needed to clarify the relationship between phenotypes and genotypes in CCD and to identify other factors that might influence the clinical features of this uncommon disease.


Assuntos
Displasia Cleidocraniana/genética , Subunidade alfa 1 de Fator de Ligação ao Core/genética , Dente Impactado/genética , Dente Supranumerário/genética , Adolescente , Adulto , Criança , Displasia Cleidocraniana/complicações , Análise Mutacional de DNA , Feminino , Mutação da Fase de Leitura , Genes Dominantes , Heterozigoto , Humanos , Masculino , Má Oclusão/etiologia , Má Oclusão/genética , Mutação de Sentido Incorreto , Linhagem , Estrutura Terciária de Proteína/genética , Dente Impactado/etiologia , Dente Supranumerário/etiologia , Adulto Jovem
4.
Clin Infect Dis ; 41(4): 544-8, 2005 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-16028166

RESUMO

The immunogenicity and tolerability of hepatitis A virus vaccine was evaluated in a group of 32 children with human immunodeficiency virus (HIV) infection and 27 children with seroreversion. After 2 doses of vaccine, 100% of children experienced seroconversion with good toleration of the vaccine. There were no differences in variation of virus load between immunized HIV-positive children and a group of 31 nonimmunized HIV-positive children with similar characteristics.


Assuntos
Infecções por HIV/imunologia , Anticorpos Anti-Hepatite A/biossíntese , Vacinas contra Hepatite A/imunologia , Tolerância Imunológica , Terapia Antirretroviral de Alta Atividade , Criança , Infecções por HIV/tratamento farmacológico , Anticorpos Anti-Hepatite A/sangue , Vacinas contra Hepatite A/administração & dosagem , Humanos
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