Search results for "Fibromas"

showing 4 items of 4 documents

Central odontogenic fibroma: retrospective study of 8 clinical cases

2010

Introduction and Objectives: The central odontogenic fibroma (COF) is a benign odontogenic tumour derived from the dental mesenchymal tissues. It is a rare tumour and only 70 cases of it have been published. Bearing in mind the rareness of the tumour, 8 new cases of central odontogenic fibroma have been found by analyzing the clinical, radiological and histopathological characteristics of COF. Patients and Method: A retrospective study was carried out on 3011 biopsies in the Service of Oral and Maxillofacial Surgery of the Dental Clinic of Barcelona University between January 1995 and March 2008. 85 odontogenic tumours were diagnosed of which 8 were central odontogenic fibroma. The radiolog…

AdultMalemedicine.medical_specialtyAdolescentDentistryOdontogenic TumorsJawsFibromaJaw neoplasmLesionYoung AdultCentral odontogenic fibromaMedicineHumansChildCàncerGeneral DentistryRetrospective StudiesTumorsCancerOral Medicine and PathologyMaxil·larsbusiness.industryMandibleRetrospective cohort studyFibromasmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Jaw NeoplasmsFibromesstomatognathic diseasesOtorhinolaryngologyRadiological weaponUNESCO::CIENCIAS MÉDICASOral and maxillofacial surgerySurgeryFemaleResearch-ArticleRadiologymedicine.symptomFibromabusiness
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Fibroma osificante maxilar: presentación de un caso y revisión de la literatura

2004

Existe un conjunto de procesos que han sido denominados genéricamente lesiones fibroóseas benignas, entre las que se encuentran la displasia fibrosa, la osteomielitis esclerosante y el fibroma osificante o cementificante. Todos estos procesos tienen un estroma fibroblástico vascular y producen una matriz calcificada que comprende desde el hueso hasta el cemento. El fibroma osificante se caracteriza por presentar un crecimiento y una tumefacción deformante de evolución lenta que generalmente aparece en la mandíbula y puede producir desplazamiento dentario precoz. Desde el punto de vista radiológico aparece generalmente como un área radiotransparente unilocular bien definida y demarcada o com…

Maxil·larsJawsOdontologíaMalalties de la bocaFibromas:CIENCIAS MÉDICAS [UNESCO]OdontologiaCiencias de la saludFibromeslesiones fibroóseas benignasMalalties dels ossosMouth diseasesDentistryUNESCO::CIENCIAS MÉDICASFibroma osificanteBone diseasesfibroma cemento-osificanteTumors
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Benign fibro-osseous lesions of the maxillas: analysis of 11 cases

2008

Introduction: A study is made of the principal characteristics of the oral lesions biopsied in our Service of Oral Surgery and histologically diagnosed as corresponding to fibro-osseous lesions of the maxillas. Patients and methods: A retrospective review was made of all the biopsies made in a Service of Oral Surgery between 1996 and 2003. The reason for consultation was analyzed, along with patient age, sex, clinical and radiological characteristics, tentative diagnosis, histological diagnosis and treatment provided. Results: A total of 1238 biopsies were performed during the study period. Of these, only 11 corresponded to benign fibro-osseous lesions (7 women and 4 men). The mean patient …

Maxil·larsUNESCO::CIENCIAS MÉDICASJawsFibromas:CIENCIAS MÉDICAS [UNESCO]Fibromes
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Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient

2008

Abstract CONTEXT: Lipase maturation factor 1 (LMF1) gene is a novel candidate gene in severe hypertriglyceridemia. Lmf1 is involved in the maturation of lipoprotein lipase (LPL) and hepatic lipase in endoplasmic reticulum. To date only one patient with severe hypertriglyceridemia and related disorders was found to be homozygous for a nonsense mutation in LMF1 gene (Y439X). OBJECTIVE: The objective of the study was to investigate LMF1 gene in hypertriglyceridemic patients in whom mutations in LPL, APOC2, and APOA5 genes had been excluded. RESULTS: The resequencing of LMF1 gene led to the discovery of a novel homozygous nonsense mutation in one patient with severe hypertriglyceridemia and rec…

Nonsynonymous substitutionMalecongenital hereditary and neonatal diseases and abnormalitiesPathologymedicine.medical_specialtyHeterozygoteNeurofibromatosis 1BiopsyDNA Mutational AnalysisMutation MissenseSoft Tissue NeoplasmsDermatologymassive soft tissue neurofibromas NeurofibromatosisBiologymedicine.disease_causeFrameshift mutationExonGenes Neurofibromatosis 1medicineSettore MED/35 - Malattie Cutanee E VenereeMissense mutationHumansNeurofibromatosisFrameshift MutationGeneSicilyGeneticsMutationHeterozygote advantageGeneral MedicineExonsMiddle Agedmedicine.diseasenervous system diseasesGene Expression Regulation NeoplasticButtocks
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