Search results for "Tooth"

showing 10 items of 910 documents

A possible inflammatory reaction in a lateral neck cyst (branchial cyst) because of odontogenic infection

1994

Abstract We present the case of a woman who suffered from an acutely infected diffuse mass in the right neck. This mass had grown rapidly after difficult extraction of a tooth. Histologic analysis of the excised material revealed a lateral neck cyst with a lymph node that showed signs of an acute inflammation near the cyst. These findings support the theory that a preexisting lateral neck cyst may be “activated” by an intraoral inflammation. The different theories of the origin of lateral neck cysts are presented and discussed in the context of the case description.

Pathologymedicine.medical_specialtyContext (language use)Odontogenic cystLymphadenitisOral and maxillofacial pathologymedicineHumansCystLymph nodeNoseOdontogenic infectionCystsFocal Infection Dentalbusiness.industryBranchial CystAnatomyMiddle Agedmedicine.diseasemedicine.anatomical_structureOtorhinolaryngologyHead and Neck NeoplasmsTooth ExtractionFemaleSurgeryBranchiomaOral SurgerybusinessNeckInternational Journal of Oral and Maxillofacial Surgery
researchProduct

Infrared Thermography. An in Vitro Study on Its Use as Diagnostic Test in Dentistry

2017

Pulp tissue consists of richly vascularized and innervated tissue with a very small circulatory access zone (the apical foramen) [1]. The amount and quality of pulp tissue can only be determined using histological techniques, which imply necrosis of the tissue [2].

Pathologymedicine.medical_specialtyNecrosisbusiness.industryDiagnostic testDentistrystomatognathic diseasesstomatognathic systemThermographyMedicineIn vitro studyPulp (tooth)Apical foramenmedicine.symptombusiness
researchProduct

Neuropathologic and morphometric studies in hereditary motor and sensory neuropathy type II with neurofilament accumulation.

1986

Histological, electron microscopic and morphometric data on sural nerve, muscle, and skin biopsies of three patients affected by autosomal dominant hereditary motor and sensory neuropathy type II with neurofilament accumulation, whose neurological, cardiological and electrophysiological data have been provided in a previous paper disclosed focally enlarged myelinated axons, due to aggregation of neurofilaments in sural nerves of all 3 biopsied patients, as well as densely packed clusters of filaments in occasional non-myelinated axons without axonal enlargement, in several fibroblasts and endothelial cells in muscle and particularly in skin. This accumulation of filaments was less pronounce…

Pathologymedicine.medical_specialtyNeurofilamentNeurologyIntermediate FilamentsSural nerveDermatologyBiologylaw.invention03 medical and health sciences0302 clinical medicineSural NervelawCharcot-Marie-Tooth DiseasemedicineHumansHereditary Sensory and Autonomic NeuropathiesIntermediate filamentCytoskeletonMyelin Sheath030304 developmental biologySkinMotor Neurons0303 health sciencesGeneral NeuroscienceMusclesGeneral MedicineAnatomymedicine.diseaseAxonsPsychiatry and Mental healthElectrophysiologyMicroscopy ElectronMuscular Atrophynervous systemUltrastructureNeurology (clinical)Electron microscopeHereditary motor and sensory neuropathy030217 neurology & neurosurgeryItalian journal of neurological sciences
researchProduct

Oral health status among Iranian veterans exposed to sulfur mustard: A case-control study

2014

Background Sulfur mustard (SM) is a chemical warfare agent that has been repeatedly used since World War I. SM has chronic and deleterious effects on different body organs such as lungs, skin and eyes. Objectives To determine dental and oral health status of chemical victims of SM who were exposed to SM during the Iraqi-Iran war. Material and Methods In this case-control study, 100 male subjects exposed to SM were chosen as cases, and 100 non-exposed volunteers were chosen as controls. These groups were selected randomly according to their referral number, and were matched regarding age. Collection of information was performed using Oral Health Assessment Form designed by the World Health O…

Pathologymedicine.medical_specialtyOdontologíachemistry.chemical_compoundmedicineTooth lossHairy TongueGeneral Dentistrybusiness.industryResearchIncidence (epidemiology)RefluxCase-control studySulfur mustardHyperplasia:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludDermatologyCommunity and Preventive DentistrychemistryUNESCO::CIENCIAS MÉDICASSalmeterolmedicine.symptombusinessmedicine.drugJournal of Clinical and Experimental Dentistry
researchProduct

The relationship between pulp calcifications and salivary gland calcifications

2014

Aim: Pulp stones are discrete calcified bodies found in the dental pulp. Sialolithasis is the most common salivary gland disease. The aim of the present study was to determine the relationship between the pulp stones and salivary gland stones. Material and Methods: 196 patients were randomly selected from the out patient department for the study. The periapical radiographs for all patients were evaluated for the presence or absence of the narrowing of dental pulp chambers and pulp canals. The intra oral occlusal radiographs were also evaluated to determine the presence or absence of salivary stones. The results were compared and analyzed using the Chi-square test ( p 0.001) and also between…

Pathologymedicine.medical_specialtyOral Medicine and PathologySalivary glandbusiness.industryResearchRadiographyPeriapical radiographyDentistryOdontologíaPulp stone:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseasesmedicine.anatomical_structurestomatognathic systemUNESCO::CIENCIAS MÉDICASPulp canalMedicinePulp (tooth)Pulp calcificationsbusinessGeneral DentistryStatistical correlation
researchProduct

Dental Pulp Polyps Contain Stem Cells Comparable to the Normal Dental Pulps

2013

Objectives: Few studies investigated the isolation of stem cells from pathologically injured dental tissues. The aim of this study was to assess the possibility of isolation of stem cells from pulp polyps (chronic hyperplastic pulpitis), a pathological tissue produced in an inflammatory proliferative response within a tooth. Study design: Pulp polyp tissues were enzymatically digested and the harvested single cells were cultured. Cultured cells underwent differentiation to adipocytes and osteoblasts as well as flowcytometric analysis for markers such as: CD90, CD73, CD105, CD45, and CD14. In addition we tried to compare other characteristics (including colonigenic efficacy, population doubl…

Pathologymedicine.medical_specialtyOral Medicine and Pathologybusiness.industryResearchMesenchymal stem cellOdontología:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludstomatognathic diseasesmedicine.anatomical_structurestomatognathic systemDental pulp stem cellsUNESCO::CIENCIAS MÉDICASmedicinePulp (tooth)CD90PulpitisBone marrowStem cellbusinessGeneral DentistryPulp polyp
researchProduct

Clinical spectrum of BICD2 mutations.

2020

Background and purpose Mutations in the BICD2 gene cause autosomal dominant lower extremity-predominant spinal muscular atrophy 2A (SMALED2A), a condition that is associated with a specific pattern of thigh and calf muscle involvement when studied by magnetic resonance imaging (MRI). Patients may present minor clinical sensory impairment, but objective sensory involvement has yet to be demonstrated. Methods We collected clinical data from 11 patients from five different families carrying mutations in BICD2. Genetic diagnosis was achieved using gene panel testing and skin biopsies were taken from two patients to study the epidermal nerve fiber density. Results In the studied patients, three …

Pathologymedicine.medical_specialtyWeaknessSensory systemNerve fiberBICD2 Charcot-Marie-Tooth hereditary motor neuropathy muscle magnetic resonance imaging spinal muscular atrophyThighmedicine.disease_causeMuscular Atrophy Spinal03 medical and health sciences0302 clinical medicineCharcot-Marie-Tooth DiseasemedicineHumans030212 general & internal medicineMuscle SkeletalMutationLegmedicine.diagnostic_testbiologybusiness.industryMagnetic resonance imagingSpinal muscular atrophymedicine.diseasebiology.organism_classificationMagnetic Resonance ImagingMediusmedicine.anatomical_structureNeurologyMutationNeurology (clinical)medicine.symptombusinessMicrotubule-Associated Proteins030217 neurology & neurosurgery
researchProduct

Bisphosphonate-related osteonecrosis. Application of adipose-derived stem cells in an experimental murine model

2019

Background Bisphosphonate-related osteonecrosis of the jaw is a pathological condition without effective established treatment and preventive strategies. The aim of this study was to analyse the effect of adipose-derived stem cells (ASC) in an experimental murine model of osteonecrosis. Material and Methods 38 Wistar rats were injected intraperitoneally with zoledronic acid. After treatment, upper jaw molars were extracted. The animals were randomly assigned to one of two groups. In the control group, saline solution was applied over the alveolar sockets after the tooth extractions. In the treatment group, ASCs were applied instead of saline solution. The control and treatment groups were s…

Pathologymedicine.medical_specialtymedicine.medical_treatmentReviewBone remodelingMice03 medical and health sciences0302 clinical medicinemedicineAnimalsRats WistarGeneral DentistryDental alveolusBisphosphonate-associated osteonecrosis of the jawBone Density Conservation AgentsDiphosphonatesbusiness.industryStem CellsImidazolesOsteonecrosis030206 dentistryBisphosphonate:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseRatsDisease Models AnimalBone Density Conservation AgentsZoledronic acidOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASTooth ExtractionBisphosphonate-Associated Osteonecrosis of the JawSurgeryOral SurgeryStem cellbusinessOsteonecrosis of the jawmedicine.drugMedicina Oral Patología Oral y Cirugia Bucal
researchProduct

Orofacial features and medical profile of eight individuals with Kabuki syndrome

2019

Background To evaluate oral, craniofacial and systemic characteristics of eight patients with Kabuki syndrome (KS), aged between 3 and 16 years old. Material and Methods In this retrospective study, medical records of all patients were reviewed for information on family history, growth and development, medications in use, general systemic complications and oral and craniofacial characteristics. Results The medical alterations found included recurrent infections such as pneumonia and otitis media (n = 6), cardiovascular malformations (n = 4), kidney abnormalities (n = 2), epilepsy (n = 2) and visual deficiency (n = 2). The individuals exhibited dental caries (n = 5), agenesis (n = 5), delaye…

Pediatricsmedicine.medical_specialtyAdolescentCleft LipDental CariesAnodontia03 medical and health sciences0302 clinical medicinemedicineMicrodontiaHumansAbnormalities MultipleCraniofacialFamily historyChildGeneral DentistryAnodontiaRetrospective StudiesTooth Abnormalitiesbusiness.industryResearch030206 dentistryEnamel hypoplasia:CIENCIAS MÉDICAS [UNESCO]Medically compromised patients in Dentistrymedicine.diseaseHematologic DiseasesCleft Palatestomatognathic diseasesOtitisVestibular DiseasesOtorhinolaryngologyChild PreschoolFaceAgenesisUNESCO::CIENCIAS MÉDICASSurgerymedicine.symptombusinessKabuki syndromeMedicina Oral Patología Oral y Cirugia Bucal
researchProduct

Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review.

2021

KBG syndrome (OMIM #148050) is a rare autosomal dominant disorder, typically characterized by macrodontia of the upper central incisors, distinct craniofacial findings, short stature, and skeletal anomalies associated with neurological involvement including intellectual disability, behaviour difficulties, and epilepsy. KBG syndrome is associated with mutations in ANKRD11 gene that plays a chromatin regulator role of histone acetylation and gene expression during neurogenesis in the embryonic brain.

Pediatricsmedicine.medical_specialtyKBGAdolescentseizureOutcome (game theory)ANKRD11EpilepsySeizuresIntellectual DisabilityMedicineHumansAbnormalities MultipleBone Diseases Developmentalbusiness.industryTooth AbnormalitiesFaciesHigh-Throughput Nucleotide SequencingGeneral MedicineKBG SYNDROMESyndromemedicine.diseaseKBG syndromeRepressor ProteinsPhenotypeNeurologySlowing EEG activityANKRD11; KBG; Seizures; Slowing EEG activity; SyndromeFemaleNeurology (clinical)businessSeizure
researchProduct