Search results for "Hyperkeratosis"

showing 10 items of 14 documents

Expression of NF-κB and IL-6 in oral precancerous and cancerous lesions: An immunohistochemical study.

2014

Background The purpose of this study was to evaluate the immunohistochemical expression of NF-κB and IL-6 in oral premalignant and malignant lesions and to investigate their possible correlation with the presence of subepithelial inflammation. Material and Methods Thirty two oral premalignant lesions, clinically compatible with leukoplakia or erythroplakia, were investigated. Microscopically, 11 of them showed hyperkeratosis and acanthosis (epithelial hyperplasia) and 21 showed dysplasia of varying degrees. Nine cases of OSCC and four control cases of normal oral mucosa were also included in the study. Immunohistochemical staining with NF-κB (p65) and IL-6 was performed. IL-6 and nuclear NF…

0301 basic medicineAdultMalePathologymedicine.medical_specialtyHyperkeratosisOdontologíaAcanthosis03 medical and health sciences0302 clinical medicineMedicineHumansGeneral DentistryLeukoplakiaAgedMouth neoplasmAged 80 and overErythroplakiaOral Medicine and Pathologybusiness.industryInterleukin-6ResearchNF-kappa BMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludImmunohistochemistrystomatognathic diseases030104 developmental biologyOtorhinolaryngologyDysplasia030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASImmunohistochemistrySurgeryFemaleMouth NeoplasmsbusinessPrecancerous ConditionsImmunostainingLeukoplakiaMedicina oral, patologia oral y cirugia bucal
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Histopathological characterization of the oral lichenoid disease subtypes and the relation with the clinical data

2016

Background: The aim of the study was to analyze the histopathological characteristics of samples with a diagnosis of oral lichenoid disease (OLD) and their link with the location and the type of clinical lesion, and the clinicopathological subtypes.

AdultMaleEpithelial dysplasiaPathologymedicine.medical_specialtyPrecancerous conditionsHyperkeratosisOral medicineLesion03 medical and health sciences0302 clinical medicineHistology PathologicalBiopsyOral and maxillofacial pathologyCarcinomaMedicineHumansGeneral DentistryAgedRetrospective StudiesAged 80 and overOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryResearchMouth -- Diseases -- DiagnosisRetrospective cohort study030206 dentistryMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesOtorhinolaryngology030220 oncology & carcinogenesisDentistryUNESCO::CIENCIAS MÉDICASSurgeryFemaleDifferential diagnosismedicine.symptombusinessLichen Planus Oral
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Histopathological findings in oral lichen planus and their correlation with the clinical manifestations

2010

Objectives: To highlight the most characteristic histopathological findings of oral lichen planus and their correlation with the clinical manifestations and forms. Study design: We performed a retrospective study of 50 biopsied and diagnosed cases of oral lichen planus obtained over a period of 11 years, spanning from May 1998 to April 2009. We analyzed the age and sex of the patient, type of lichen planus, location and different histopathological findings, comparing them with the clinical lesions. Results: Seventy eight percent of the patients are female and 22% are male, with an average age of 56.06 years for both sexes. The most frequent clinical form is reticular, present in 78% of the …

AdultMalePathologymedicine.medical_specialtyEpithelial dysplasiaHyperkeratosisAcanthosisHydropic degenerationstomatognathic systemOral and maxillofacial pathologymedicineAtypiaHumansskin and connective tissue diseasesGeneral DentistryAgedRetrospective StudiesAged 80 and overintegumentary systembusiness.industryMiddle AgedHyperplasia:CIENCIAS MÉDICAS [UNESCO]medicine.diseasestomatognathic diseasesOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASFemaleSurgeryOral lichen planusbusinessLichen Planus Oral
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The Effectiveness of Laser-Assisted Surgical Excision of Leukoplakias and Hyperkeratosis of Oral Mucosa: A Case Series in A Group of Patients

2019

Introduction: In the different branches of dentistry, the use of laser to solve different clinical situations is increasing due to numerous advantages that have been studied in literature since the 70s. Leucoplakia and hyperkeratosis can benefit from laser-assisted treatment. In most cases biopsy sampling, histological examination and, if no malignant cells are present, the follow-up is needed. However, even if the lesion is free of dysplasia patients often ask to eliminate these white spots that are always a cause of concern. Aim: From these numerous requests comes the idea of setting up a laser-assisted protocol as less invasive as possible to be offered to patients. The aim of the study …

AdultMalemedicine.medical_specialtyHealth Toxicology and MutagenesisleucoplakiaHyperkeratosisCirurgia dentallcsh:Medicineoral medicinehyperkeratosis; laser; leucoplakia; oral medicine; oral surgeryArticleNOLesion03 medical and health sciences0302 clinical medicineBiopsymedicineHumansSampling (medicine)Oral mucosaHyperplasiahyperkeratosismedicine.diagnostic_testbusiness.industryMedical recordlcsh:RMouth MucosaPublic Health Environmental and Occupational HealthhyperkeratosiMED/28 - MALATTIE ODONTOSTOMATOLOGICHE030206 dentistryMiddle Agedmedicine.diseaseSurgerylasermedicine.anatomical_structureDysplasiaMED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICAFemaleLasers Semiconductormedicine.symptombusinessOral medicineLeukoplakia030215 immunologyoral surgery
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Hypohidrotic Ectodermal Dysplasia with total anodontia: A case report

2011

Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. The triad of nail dystrophy, alopecia or hypotrichosis and palmoplantar hyperkeratosis is usually accompanied by a lack of sweat glands and a partial or complete absence of primary and/ or permanent dentition. A case report illustrating the prosthetic rehabilitation of a seven year old boy with hypohidrotic ectodermal dysplasia associated with total anodontia is presented.

Ectodermal dysplasiamedicine.medical_specialtyanimal structuresPalmoplantar hyperkeratosisintegumentary systembusiness.industryPermanent dentitionOdontologíaEctoderm:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludDermatologymedicine.anatomical_structureTotal anodontiaUNESCO::CIENCIAS MÉDICASembryonic structuresmedicineHypotrichosisHypohidrotic ectodermal dysplasiabusinessGeneral DentistryNAIL DYSTROPHYJournal of Clinical and Experimental Dentistry
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Progressive symmetric erythro-keratosis associated with oligodontia, severe caries, disturbed hair growth and ectopic nail: a new syndrome?

2008

A 7-year-old girl had well-demarcated erythematous plaques covered with white pityriasiform scales which were symmetrically distributed and involved the extensor surfaces of the extremities as well as the abdomen, buttocks and face. Histological examination showed marked hyperkeratosis with parakeratosis, and a thickened granular cell layer, mild acanthosis and slight lymphocytic infiltration surrounding the papillary blood vessels, compatible with a diagnosis of progressive symmetrical erythrokeratodermia. Remarkably, a keratotic excrescence similar to a normal nail plate involved the tip of the nose since the age of 6 months. Moreover, occipital hairlessness, oligodontia and severe caries…

HyperkeratosisAcanthosisDermatologyOligodontiaDental CariesProgressive symmetric erythrokeratodermiaDiagnosis DifferentialErythrokeratodermiaErythematous plaqueSettore MED/35 - Malattie Cutanee E VenereemedicineHumansAbnormalities MultipleParakeratosisChildAnodontiaHyperkeratosis Epidermolyticbusiness.industryProgressive symmetric erythro-keratosis new syndromeAnatomySyndromeNail platemedicine.diseaseNailsFemalemedicine.symptombusinessHairDermatology (Basel, Switzerland)
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Evaluation of cell proliferation rate in non-dysplastic leukoplakias

2008

Objective: Analyze whether the most frequent cases of non-dysplastic leukoplakias, hyperkeratosis (H), acanthosis (A), and hyperkeratosis with acanthosis (HA) have similar cell proliferation rates and to compare them with epithelial dysplastic (ED) leukoplakias and normal oral epithelium (NOE).Study design: The sample comprised 10 cases of normal oral epithelium, 10 cases of hyperkeratosis, 10 cases of acanthosis, 10 cases of hyperkeratosis with acanthosis and 10 cases of epithelial dysplasia. The mean number of AgNORs per nucleus (mAgNOR) and the mean percentage of cells with 1, 2, 3 and 4 or more AgNORs per nucleus (pAgNOR) were recorded. Results: The results of mAgNOR showed differences …

MaleEpithelial dysplasiaPathologymedicine.medical_specialtyHyperkeratosisAcanthosisHyperkeratosisEpithelial dysplasiaAcanthosisBasal (phylogenetics)Biological profileProliferation rateOral and maxillofacial pathologyHumansMedicineLeucoplasia bucalGeneral DentistryCell proliferationCell ProliferationLeukoplakiabusiness.industryAntigens NuclearProliferação celularMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Doencas [Mucosa bucal]AgNORstomatognathic diseasesOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASPatologia bucalFemaleSurgeryLeukoplakia OralbusinessLeukoplakia
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Key features and clinical variability of COG6-CDG

2015

The conserved oligomeric Golgi (COG) complex consists of eight subunits and plays a crucial role in Golgi trafficking and positioning of glycosylation enzymes. Mutations in all COG subunits, except subunit 3, have been detected in patients with congenital disorders of glycosylation (CDG) of variable severity. So far, 3 families with a total of 10 individuals with biallelic COG6 mutations have been described, showing a broad clinical spectrum. Here we present 7 additional patients with 4 novel COG6 mutations. In spite of clinical variability, we delineate the core features of COG6-CDG i.e. liver involvement (9/10), microcephaly (8/10), developmental disability (8/10), recurrent infections (7…

MaleMicrocephalyGlycosylationAdolescentEndocrinology Diabetes and MetabolismProtein subunitHyperkeratosisMolecular Sequence DataGolgi ApparatusCase ReportsResearch SupportBiochemistryConserved oligomeric Golgi complexYoung AdultEndocrinologyCogCongenital Disorders of GlycosylationGeneticsJournal ArticleMedicineHumansNon-U.S. Gov'tChildMolecular BiologyExome sequencingGenetic Association StudiesGeneticsbusiness.industryConserved oligomeric Golgi complexResearch Support Non-U.S. Gov'tHigh-Throughput Nucleotide SequencingInfantCongenital disorder of glycosylationmedicine.diseasePhenotypeAdaptor Proteins Vesicular TransportPhenotypeCOG6MutationMicrocephalyFemaleCDGbusinessCongenital disorder of glycosylation
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Visualization of Keratin with Diffuse Reflectance and Autofluorescence Imaging and Nonlinear Optical Microscopy in a Rare Keratinopathic Ichthyosis.

2021

Keratins are one of the main fluorophores of the skin. Keratinization disorders can lead to alterations in the optical properties of the skin. We set out to investigate a rare form of keratinopathic ichthyosis caused by KRT1 mutation with two different optical imaging methods. We used a newly developed light emitting diode (LED) based device to analyze autofluorescence signal at 405 nm excitation and diffuse reflectance at 526 nm in vivo. Mean autofluorescence intensity of the hyperkeratotic palmar skin was markedly higher in comparison to the healthy control (162.35 vs. 51.14). To further assess the skin status, we examined samples from affected skin areas ex vivo by nonlinear optical micr…

MaleNonlinear Optical MicroscopyHyperkeratosisautofluorescencelcsh:Chemical technologyBiochemistryAnalytical Chemistry030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineIn vivoKeratinmedicineHumanslcsh:TP1-1185Electrical and Electronic EngineeringInstrumentationkeratinSkinchemistry.chemical_classificationHyperkeratosis Epidermolyticintegumentary systemhyperkeratosisChemistryCommunicationOptical ImagingLEDnonlinear microscopyepidermolytic ichthyosismedicine.diseasediffuse reflectanceFluorescenceNonlinear optical microscopyAtomic and Molecular Physics and OpticsAutofluorescencemedicine.anatomical_structure030220 oncology & carcinogenesisChild Preschoolmultiphoton microscopyhistopathologyKeratinsKRT1EpidermisDiffuse reflectionBiomedical engineeringSensors (Basel, Switzerland)
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IL-6 Regulates Neutrophil Microabscess Formation in IL-17A-Driven Psoriasiform Lesions

2014

The lack of a generally accepted animal model for human psoriasis has hindered progress with respect to understanding the pathogenesis of the disease. Here we present a model in which transgenic IL-17A expression is targeted to the skin in mice, achievable after crossing our IL-17A(ind) allele to the K14-Cre strain. K14-IL-17A(ind/+) mice invariably develop an overt skin inflammation bearing many hallmark characteristics of human psoriasis including dermal infiltration of effector T cells, formation of neutrophil microabscesses, and hyperkeratosis. IL-17A expression in the skin results in upregulated granulopoiesis and migration of IL-6R-expressing neutrophils into the skin. Neutralization …

Pathologymedicine.medical_specialty1303 BiochemistryNeutrophilsT-LymphocytesHyperkeratosisGene Expression610 Medicine & healthInflammationDermatology10263 Institute of Experimental ImmunologyBiochemistryGranulopoiesis2708 Dermatology1307 Cell BiologyPathogenesisMicePsoriasis1312 Molecular BiologymedicineAnimalsPsoriasisMicroabscessMolecular BiologyMice Knockoutintegumentary systemInterleukin-6business.industryMacrophagesInterleukin-17Cell Biologymedicine.diseaseReceptors Interleukin-6AbscessDisease Models AnimalImmunology570 Life sciences; biologyEpidermismedicine.symptombusinessInfiltration (medical)GranulocytesSignal TransductionEpidermal thickeningJournal of Investigative Dermatology
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