Search results for " Dysplasia"

showing 10 items of 206 documents

Application of remote online learning in oral histopathology teaching in China

2021

Background The aim of this study was to investigate the application of remote learning and virtual microscopy in oral histopathology teaching, a unique experience in China. The oral histopathology teaching in Nanjing Medical University has been extraordinary. Material and Methods 98 third-year dental students of Grade 2016 took oral histopathology theoretical course face-to-face in 2019 (Traditional group). The 94 participants of Grade 2017 took online oral histopathology course using digital methods(E-Learning platform and Virtual Simulation Experiment Teaching Center for Dentistry) in 2020. During the practical laboratory sessions, the students in both Traditional group and Online group o…

medicine.medical_specialtyChinaeducationStudents DentalRemote learningVirtual technologyEducation Distanceoral lichen planusepithelial dysplasiamedicineHumansLearningGeneral DentistryEducation DentalUNESCO:CIENCIAS MÉDICASMedical educationOral Medicine and PathologyOnline learningResearchQuestionnaireoral cancerTest (assessment)OtorhinolaryngologySurgeryHistopathologyPsychologyVirtual microscopyMedicina Oral, Patología Oral y Cirugía Bucal
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Professional diagnostic delay in osteosarcomas of the jaws

2020

A series of 20 consecutive patients with an osteosarcoma of the jaws has been evaluated with regard to possible professional diagnostic delay. When set at an arbitrarily chosen period beyond three months, professional delay occurred in 15 patients, the mean being 21 months and the median 11 months. In five of the 15 patients a wrong diagnosis has been rendered on the biopsy specimen, being fibrous dysplasia (2x), osteoma (2x) and, in case of palatomaxillary swelling, pleomorphic adenoma (1x). In the other ten patients the initial clinicoradiographic features were misleading and apparently not indicative of a malignancy, except for one patient in whom a distinct widening of the periodontal l…

medicine.medical_specialtyDelayed DiagnosisBone NeoplasmsDelayed diagnosisMalignancyPleomorphic adenoma03 medical and health sciences0302 clinical medicineSDG 3 - Good Health and Well-beingBiopsymedicineHumansGeneral DentistryOsteomaOsteosarcomamedicine.diagnostic_testbusiness.industryResearchFibrous dysplasia030206 dentistryPrognosisMedically compromised patients in Dentistry:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseOtorhinolaryngologyUNESCO::CIENCIAS MÉDICAS/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingOsteosarcomaSurgeryRadiologybusiness
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Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical rep…

2021

Abstract Introduction Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome, also known as Hay-Wells syndrome, is a rare genetic syndrome with ectodermal dysplasia. About 100 patients have been reported to date. It is associated to a heterozygous mutation of the tumor protein p63 (TP63) gene, located on chromosome 3q28. Typical clinical manifestations include: filiform ankyloblepharon adnatum (congenital adherence of the eyelids), ectodermal abnormalities (sparse and frizzy hair, skin defects, nail alterations, dental changes and hypohidrosis), and cleft lip/palate. Diagnostic suspicion is based on clinical signs and confirmed by genetic testing. Patient’s presentation We hereb…

medicine.medical_specialtyEctodermal dysplasiaHay–Wells syndromeCleft LipAnkyloblepharonMutation MissenseErythrodermaCase ReportEctodermal dysplasiaPediatricsRJ1-570TP63medicineMissense mutationHumansEye Abnormalitiesbusiness.industryTumor Suppressor ProteinsAEC syndromeInfant NewbornTumor protein p63 geneEyelidsmedicine.diseaseAnkyloblepharon-ectodermal defects-cleft lip/palate syndromeDermatologyCleft Palatemedicine.anatomical_structureHay-Wells syndromeScalpAgenesisFemaleAEC syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Congenital skin disorders Ectodermal dysplasia Hay-Wells syndrome Tumor protein p63 genebusinessTranscription FactorsCongenital skin disordersItalian journal of pediatrics
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Increased risk for cervical disease progression of French women infected with the human papillomavirus type 16 E6-350G variant.

2006

Abstract To test the significance of human papillomavirus (HPV) type 16 and HPV16 E6 variants as risk factors for viral persistence and progression to high-grade lesion, we did a nested case-control study within a cohort study of >15,000 Caucasian French women. Three groups infected with high-risk HPV were compared: (a) women with cleared infection (controls, n = 201), (b) women with persistent infection (cases, n = 87), and (c) women who progressed into high-grade lesion (cases, n = 58). Women with persistent HPV infection and those that progressed into high-grade lesions were likelier to harbor HPV16 than other high-risk HPV types [odds ratio (OR), 2.4; 95% confidence interval (95%…

medicine.medical_specialtyEpidemiologyUterine Cervical NeoplasmsCervical intraepithelial neoplasiaLesionCohort StudiesRisk FactorsInternal medicineEpidemiologymedicineOdds RatioHumansRisk factorbusiness.industryPapillomavirus InfectionsHPV infectionvirus diseasesOdds ratioOncogene Proteins Viralmedicine.diseaseUterine Cervical DysplasiaRepressor ProteinsOncologyCase-Control StudiesImmunologyDisease ProgressionFemaleViral diseaseFrancemedicine.symptombusinessCohort studyCancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
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Human papilloma virus genotypes in dysplasia and epithelial hyperplasia of oral cavity using the luminex xmap technology. A multicenter study

2019

Background Oral cancer associated with high risk (HPV-HR) human papilloma virus (HPV) has been increasing. HPV-HR has been associated with epithelial dysplasia, however, little information exists on its frequency in epithelial hyperplasia lesions. The aim of this study is to compare HPV genotypes in dysplastic and hyperplastic lesions of oral cavity. Material and Methods Two hundred and fifty oral lesions: 131 dysplasia and 119 hyperplasia from two regions of Colombia were evaluated. One hundred seventy-four coming from urban area and 104 from a high risk population to oral cancer from a rural area. HPV was identified by qPCR and Twenty-four HPVs genotypes were evaluated by Luminex® technol…

medicine.medical_specialtyEpithelial dysplasiaGenotypePopulationEpithelial dysplasiaGastroenterology03 medical and health sciences0302 clinical medicineEpithelial hyperplasiaInternal medicineGenotypeEnsayo clínicomedicineHumansPapillomaviridaeeducationPapillomaviridaeGeneral DentistryOral Dysplasiaeducation.field_of_studyOral Medicine and PathologyHyperplasiabiologybusiness.industryResearchPapillomavirus InfectionsCancervirus diseasesElectroforesis en gel bidimensional030206 dentistryHyperplasiamedicine.diseasebiology.organism_classification:CIENCIAS MÉDICAS [UNESCO]female genital diseases and pregnancy complicationsEnfermedades de la bocaOtorhinolaryngologyDysplasiaUNESCO::CIENCIAS MÉDICASSurgeryHPV-genotypesbusiness
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The efficacy of photodynamic therapy in rat tongue dysplasia

2017

Background Photodynamic therapy (PDT) using 5-aminolevulinic acid (ALA) has previously shown promising results in cancerous cell destruction. The present study was conducted to evaluate the efficacy of this treatment option on oral epithelial dysplasia in Wistar rats. Furthermore, microscopic effects of systemic versus topical administration of ALA before laser illumination was assessed. Material and Methods Thirty male Wistar rats (200- 250 grams) were used in the present study. Tongue dysplasia was induced by a daily delivery of a 20 ppm solution of 4-nitroquinoline -1- oxide (4NQO) for 3 months. Then, rats were divided into 3 groups of 10 including, group 1 that was received systemic ALA…

medicine.medical_specialtyEpithelial dysplasiaOral Medicine and Pathologybusiness.industryResearchmedicine.medical_treatmentPhotodynamic therapy:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseGastroenterologyRat Tonguemedicine.anatomical_structureDysplasiaTongueInternal medicineUNESCO::CIENCIAS MÉDICASCancer cellmedicineEffective treatmentLaser illuminationbusinessGeneral DentistryJournal of Clinical and Experimental Dentistry
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Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype.

2020

Background: Pathogenic variants in the filamin C (FLNC) gene are associated with inherited cardiomyopathies including dilated cardiomyopathy with an arrhythmogenic phenotype. We evaluated FLNC variants in arrhythmogenic cardiomyopathy (ACM) and investigated the disease mechanism at a molecular level. Methods: 120 gene-elusive ACM patients who fulfilled diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy (ARVC) were screened by whole exome sequencing. Fixed cardiac tissue from FLNC variant carriers who had died suddenly was investigated by histology and immunohistochemistry. Results: Novel or rare FLNC variants, four null and five variants of unknown significance, were id…

medicine.medical_specialtyFilaminsCardiomyopathyContrast MediaGadolinium030204 cardiovascular system & hematologyVentricular tachycardiaSudden deathRight ventricular cardiomyopathy03 medical and health sciences0302 clinical medicineCardiac magnetic resonance imagingInternal medicinemedicineHumansCor030212 general & internal medicineFLNCcardiovascular diseasesArrhythmogenic Right Ventricular DysplasiaExome sequencingmedicine.diagnostic_testbusiness.industryDilated cardiomyopathymedicine.diseasePatologiaPhenotypeMutationCardiologyCardiomyopathiesCardiology and Cardiovascular Medicinebusiness
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Die Hochenergetische Extrakorporale Stoßwellentherapie (ESWT) in der Behandlung von Pseudarthrosen

2008

PROBLEM The success rate of high-energy extracorporal shock wave therapy in the treatment of non-unions in comparison to the "golden standard" surgery is still unclear. METHOD In a prospective study, 3000 impulses with an energy density of 0.6 mJ/mm2 were applied with an experimental device to the pseudarthrosis in 52 patients. RESULTS The mean duration of pseudarthrosis was 13 months. A mean of 2.5 surgical interventions had already been performed. Bony union was achieved in 52% of our patients after an average of 3.3 months. Failures especially were found in the atrophic type of pseudarthrosis as well as in congenital bone disorders like fibrous dysplasia or osteogenesis imperfecta. No se…

medicine.medical_specialtyHigh energyExtracorporeal shock wave therapybusiness.industryFibrous dysplasiamedicine.diseaseSurgeryPseudarthrosisOsteogenesis imperfectamedicineEnergy densityOrthopedics and Sports MedicineSurgeryProspective cohort studybusinessComplicationZeitschrift für Orthopädie und ihre Grenzgebiete
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Endoscopic Resection for High-Grade Dysplasia in Barrett’s Esophagus

2005

Endoscopic resection (ER) has gained more and more importance in the treatment of high grade dysplasia (HGD) in Barrett's esophagus over the last few years. The choice of the different available techniques depends on the macroscopic type of the lesion and the personal experience of the endoscopist. But the "suck and cut"-technique with ligation device or cap should be favoured to normal strip biopsy in the esophagus because of the size of the resected specimen and its technical feasibility. Several studies demonstrate the effectivity and safety of ER in patients with HGD, therefore ER should be the treatment of choice in these patients.

medicine.medical_specialtyHigh grade dysplasiabusiness.industryGeneral surgeryGastroenterologyEsophageal cancermedicine.diseasedigestive system diseasesLesionmedicine.anatomical_structureBarrett's esophagusmedicineRadiology Nuclear Medicine and imagingIn patientEndoscopic resectionRadiologymedicine.symptomEsophagusLigationbusinessTechniques in Gastrointestinal Endoscopy
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Congenital malformations and perinatal morbidity associated with intestinal neuronal dysplasia.

1998

A close relation between different forms of dysganglionosis such as intestinal neuronal dysplasia (IND) type B and aganglionosis has been established. No systematic analysis of other malformations and diseases accompanying IND has been made as yet. Congenital malformations and perinatal morbidity were analyzed in 109 patients with IND seen at the Department of Pediatric Surgery in Mainz from 1977 to 1996. IND was associated with Hirschsprung's disease in 47 cases; 22 children with IND had other abdominal malformations, including anal atresia, rectal stenosis, sigmoidal stenosis, ileal atresia, pyloric stenosis, and esophageal atresia. A cystic bowel duplication, a choledochal cyst, and a pe…

medicine.medical_specialtyIntestinal AtresiaPyloric stenosisCongenital AbnormalitiesMedicineHumansAbnormalities MultipleHirschsprung DiseaseChildHirschsprung's diseaseIntestinal neuronal dysplasiabusiness.industryIntestinal atresiaInfant NewbornIleal AtresiaInfantGeneral MedicineSubmucous Plexusbiochemical phenomena metabolism and nutritionmedicine.diseasedigestive system diseasesSurgeryIntestinesAnal atresiaAtresiaPediatrics Perinatology and Child HealthNecrotizing enterocolitisSurgeryDown SyndromeMorbiditybusinessPediatric surgery international
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