1.Nonsurgical endodontic retreatment of fused teeth with transposition: a case report.
Miguel Agostinho Beco Pinto CARDOSO ; Rita Brandão NOITES ; Miguel André Duarte MARTINS ; Manuel Pedro da Fonseca PAULO
Restorative Dentistry & Endodontics 2016;41(2):148-153
Tooth transposition is a disorder in which a permanent tooth develops and erupts in the normal position of another permanent tooth. Fusion and gemination are developmental disturbances presenting as the union of teeth. This article reports the nonsurgical retreatment of a very rare case of fused teeth with transposition. A patient was referred for endodontic treatment of her maxillary left first molar in the position of the first premolar, which was adjacent to it on the distobuccal side. Orthopantomography and periapical radiography showed two crowns sharing the same root, with a root canal treatment and an associated periapical lesion. Tooth fusion with transposition of a maxillary molar and a premolar was diagnosed. Nonsurgical endodontic retreatment was performed. At four yr follow-up, the tooth was asymptomatic and the radiolucency around the apical region had decreased, showing the success of our intervention. The diagnosis and treatment of fused teeth require special attention. The canal system should be carefully explored to obtain a full understanding of the anatomy, allowing it to be fully cleaned and obturated. Thermoplastic techniques were useful in obtaining hermetic obturation. A correct anatomical evaluation improves the set of treatment options under consideration, leading to a higher likelihood of esthetically and functionally successful treatment.
Bicuspid
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Crowns
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Dental Pulp Cavity
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Diagnosis
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Follow-Up Studies
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Fused Teeth*
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Humans
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Molar
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Radiography
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Radiography, Panoramic
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Retreatment*
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Tooth
2.Molecular diversity of the VP2 of Carnivore protoparvovirus 1 (CPV-2) of fecal samples from Bogotá
Cristian Camilo GALVIS ; Tatiana JIMENEZ-VILLEGAS ; Diana Patricia REYES ROMERO ; Alejandro VELANDIA ; Sueli TANIWAKI ; Sheila Oliveira de SOUZA SILVA ; Paulo BRANDÃO ; Nelson Fernando SANTANA-CLAVIJO
Journal of Veterinary Science 2022;23(1):e14-
Background:
Carnivore protoparvovirus 1, also known as canine parvovirus type 2 (CPV-2), is the main pathogen in hemorrhagic gastroenteritis in dogs, with a high mortality rate. Three subtypes (a, b, c) have been described based on VP2 residue 426, where 2a, 2b, and 2c have asparagine, aspartic acid, and glutamic acid, respectively.
Objectives:
This study examined the presence of CPV-2 variants in the fecal samples of dogs diagnosed with canine parvovirus in Bogotá.
Methods:
Fecal samples were collected from 54 puppies and young dogs (< 1 year) that tested positive for the CPV through rapid antigen test detection between 2014–2018. Molecular screening was developed for VP1 because primers 555 for VP2 do not amplify, it was necessary to design a primer set for VP2 amplification of 982 nt. All samples that were amplified were sequenced by Sanger. Phylogenetics and structural analysis was carried out, focusing on residue 426.
Results:
As a result 47 out of 54 samples tested positive for VP1 screening, and 34/47 samples tested positive for VP2 980 primers as subtype 2a (n = 30) or 2b (n = 4); subtype 2c was not detected. All VP2 sequences had the amino acid, T, at 440, and most Colombian sequences showed an S514A substitution, which in the structural modeling is located in an antigenic region, together with the 426 residue.
Conclusions
The 2c variant was not detected, and these findings suggest that Colombian strains of CPV-2 might be under an antigenic drift.
3.Antimicrobial activity of calcium hydroxide and chlorhexidine on intratubular Candida albicans.
Ronan Jacques Rezende DELGADO ; Thaís Helena GASPAROTO ; Carla Renata SIPERT ; Claudia Ramos PINHEIRO ; Ivaldo Gomes de MORAES ; Roberto Brandão GARCIA ; Marco Antônio Hungaro DUARTE ; Clóvis Monteiro BRAMANTE ; Sérgio Aparecido TORRES ; Gustavo Pompermaier GARLET ; Ana Paula CAMPANELLI ; Norberti BERNARDINELI
International Journal of Oral Science 2013;5(1):32-36
This study investigated the efficacy of calcium hydroxide and chlorhexidine gel for the elimination of intratubular Candida albicans (C. albicans). Human single-rooted teeth contaminated with C. albicans were treated with calcium hydroxide, 2% chlorhexidine gel, calcium hydroxide plus 2% chlorhexidine gel, or saline (0.9% sodium chloride) as a positive control. The samples obtained at depths of 0-100 and 100-200 µm from the root canal system were analyzed for C. albicans load by counting the number of colony forming units and for the percentage of viable C. albicans using fluorescence microscopy. First, the antimicrobial activity of calcium hydroxide and the 2% chlorhexidine gel was evaluated by counting the number of colony forming units. After 14 days of intracanal medication, there was a significant decrease in the number of C. albicans colony forming units at a depth of 0-100 µm with chlorhexidine treatment either with or without calcium hydroxide compared with the calcium hydroxide only treatment. However, there were no differences in the number of colony forming units at the 100-200 µm depth for any of the medications investigated. C. albicans viability was also evaluated by vital staining techniques and fluorescence microscopy analysis. Antifungal activity against C. albicans significantly increased at both depths in the chlorhexidine groups with and without calcium hydroxide compared with the groups treated with calcium hydroxide only. Treatments with only chlorhexidine or chlorhexidine in combination with calcium hydroxide were effective for elimination of C. albicans.
Antifungal Agents
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administration & dosage
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pharmacology
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Calcium Hydroxide
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administration & dosage
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pharmacology
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Candida albicans
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drug effects
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Chlorhexidine
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administration & dosage
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pharmacology
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Colony Count, Microbial
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Coloring Agents
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Dental Pulp Cavity
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microbiology
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Drug Combinations
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Humans
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Microbial Viability
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drug effects
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Microscopy, Electron, Scanning
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Microscopy, Fluorescence
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Root Canal Irrigants
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administration & dosage
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pharmacology
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Root Canal Preparation
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methods
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Smear Layer
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Time Factors