The aim of this study was to evaluate the influence of different restorative procedures on the fracture resistance of endodontically treated teeth submitted to intracoronal bleaching. Fifty upper central incisors were distributed into 5 groups: GI -healthy teeth; GII -endodontically treated teeth sealed with Coltosol; GIII -endodontically treated teeth bleached and sealed with Coltosol; GIV -endodontically treated teeth bleached and restored with composite resin; and GV -endodontically treated teeth bleached and restored with a fiberglass post and composite resin. In the bleached specimens, a cervical seal was made prior to bleaching with 38% hydrogen peroxide. The gel was applied on the buccal surface and in the pulp chamber, and was then light-activated for 45 s. This procedure was repeated three times per session for four sessions, and each group was submitted to the restorative procedures described above. The specimens were submitted to fracture resistance testing in a universal testing machine. There were statistically significant differences among the groups (p < 0.05). The mean value found for GIII was the lowest (0.32 kN) and was significantly different from the values found for GI (0.75 kN), GII (0.67 kN), GIV (0.70 kN), and GV (0.72 kN), which were not significantly different from each other (p > 0.05). The restorative procedures using composite resin were found to successfully restore the fracture resistance of endodontically treated and bleached teeth.

The aim of this study was to analyze the transplant efficiency of non-pedicled buccal fat pad graft (BFPG) for the treatment of Miller Class I or II gingival recessions (GRs) and to compare these results with those of subepithelial connective tissue graft (SCTG), which is considered the gold standard. Twelve patients with Miller Class I or II (≥2 mm) bilateral recessions in maxillary premolars or canines were selected. Recessions were randomly assigned to receive SCTG or BFPG. The clinical parameters evaluated at baseline and at 1, 3, and 6 months postoperatively included gingival index, plaque index, probing depth, GR, clinical attachment level, width of keratinized tissue, thickness of keratinized tissue and gingival margin to the acrylic guide. None of the evaluated clinical parameters differed significantly between the groups. At all evaluated postoperative time-points, both groups exhibited statistically significant differences in GR and gingival margin to the acrylic guide compared to baseline. Six months after surgery, the mean percentages of root coverage were 67.5% and 87.5% in the BFPG and SCTG groups respectively. In both groups, complete root coverage was observed in 50% of cases 6 months after surgery. The results presented herein indicate that the use of BFPG transplant has clinical similarities with SCTG and both may be considered as clinically successful methods for treating Miller Class I and II GRs.

ABSTRACT:This study compared the resistance to removal by traction of abraded cylindrical metal cast posts of Cu-Al (Goldent-LA). The posts had constant length (9 mm) and three different diameters (0.9, 1.3 and 1.7 mm), and were cemented with zinc phosphate cement. The crowns of 36 sound maxillary canines were sectioned, the roots were immersed in resin blocks and the root canals were endodontically treated. The teeth were divided into three groups to be prepared and standardized with the use of a parallelometer with the following burs: Group 1 -Largo n. 2; Group 2 -Largo n. 4; Group 3 -Largo n. 6. The posts were molded with chemically activated resin and after casting they were abraded and their dimensions were confirmed with a digital caliper. After cementation of the posts in the prepared root canals, the samples were kept at 37ºC in distilled water for 7 days and subsequently submitted to the traction test in a universal testing machine (Instron 4444). The results showed no statistical difference between the groups. Diameter variation (0.9 mm, 1.3 mm and 1.7 mm) in abraded cylindrical posts cemented with zinc phosphate did not affect resistance to removal. DESCRIPTORS: Tensile strength; Post and core technique. RESUMO:Este estudo in vitro comparou a resistência à remoção por tração de núcleos metálicos fundidos em liga de Cu-Al (Goldent-LA) cilíndricos, jateados, de comprimento constante igual a 9 mm, cimentados com cimento de fosfato de zinco e com três diferentes diâmetros: 0,9 mm, 1,3 mm e 1,7 mm. Trinta e seis caninos superiores hígi-dos tiveram suas coroas seccionadas, sendo as raízes incluídas em blocos de resina acrílica, e os canais, tratados endodonticamente. Os dentes foram divididos em três grupos para serem preparados e padronizados com o auxílio de um paralelômetro com as seguintes brocas: Grupo 1 -Largo nº 2; Grupo 2 -Largo nº 4; Grupo 3 -Largo nº 6. Os núcleos foram moldados com resina acrílica ativada quimicamente e, após a fundição, foram jateados e tiveram as suas dimensões conferidas com um paquímetro digital. Após a cimentação, os corpos-de-prova foram armazenados em água destilada durante 7 dias, em estufa a 37ºC e, posteriormente, submetidos a teste de tração em uma máquina universal de ensaios Instron 4444. Com a análise estatística dos resultados, pôde-se concluir que não houve diferença estatisticamente significante entre os grupos testados. A variação do diâmetro em núcleos cilíndricos jateados cimentados com fosfato de zinco não afetou a resistência à remoção.

Singleton Merten Syndrome is a rare disease characterized by the presence of the dental dysplasia phenotype, calcifications in the aorta, progressive wear and loss of bone protein (osteoporosis) in the hands and feet. Patients have muscle weakness, poor motor development, abnormal dentition, deformities of the feet and hands, and skin lesions. Objective: This report describes the maxillomandibular rehabilitation of a patient with Singleton Merten Syndrome and an allergic reaction to the acrylic resin through maxillary overdenture and mandibular partial removable denture. Case report: Female patient, 18 years old, with clinical characteristics of Singleton Merten Syndrome and allergic reaction to acrylic resin, with complaints of loss of function and esthetics due to the absence of several teeth, but with the presence of unerupted maxillary and mandibular tooth buds. Maxillary overdenture and mandibular removable partial denture were made of polyethylene. Conclusion: The rehabilitation treatment with maxillary overdenture and mandibular partial removable denture provided better facial muscle support, restoring masticatory function and facial esthetics. With this treatment, it was possible to reestablish patient’s satisfaction and self-esteem due to the correct construction of the prostheses, and minimize hypersensitivity reactions in the oral mucosa, which allowed the use of these prostheses by the patient without any complications.

Introduction: Singleton Merten Syndrome is a rare disease characterized by the presence of the dental dysplasia phenotype, calcifications in the aorta, progressive wear and loss of bone protein (osteoporosis) in the hands and feet. Patients have muscle weakness, poor motor development, abnormal dentition, deformities of the feet and hands, and skin lesions. Objective: This report describes the maxillomandibular rehabilitation of a patient with Singleton Merten Syndrome and an allergic reaction to the acrylic resin through maxillary overdenture and mandibular partial removable denture. Case report: Female patient, 18 years old, with clinical characteristics of Singleton Merten Syndrome and allergic reaction to acrylic resin, with complaints of loss of function and esthetics due to the absence of several teeth, but with the presence of unerupted maxillary and mandibular tooth buds. Maxillary overdenture and mandibular removable partial denture were made of polyethylene. Conclusion: The rehabilitation treatment with maxillary overdenture and mandibular partial removable denture provided better facial muscle support, restoring masticatory function and facial esthetics. With this treatment, it was possible to reestablish patient's satisfaction and self-esteem due to the correct construction of the prostheses, and minimize hypersensitivity reactions in the oral mucosa, which allowed the use of these prostheses by the patient without any complications.