Search results for "Dysplasia"

showing 10 items of 310 documents

Florid cemento-osseous dysplasia : report of 2 cases

2018

Introduction Florid cemento-osseous dysplasia is a non-neoplastic fibro-osseous lesion which often has an asymptomatic slow growth. Unfortunately, these lesions are usually diagnosed through routine radiographic examination. The aim of this study was to describe the main clinical, radiological and histological characteristics of two case reports diagnosed with florid cemento-osseous dysplasia. Case reports Two cases of florid cemento-osseous dysplasia with different clinical and radiological features were presented. Panoramic radiographs showed multiple radiopacities compatible with fibro-osseous lesions in distinct areas of the maxillary bones. The histological study revealed a sclerotic m…

musculoskeletal diseasesmedicine.medical_specialtyRadiographyCase ReportFibrous tissueMaxillary BonesAsymptomaticLesion03 medical and health sciences0302 clinical medicinestomatognathic systemmedicineOssosDisplàsia fibrosa òssia030223 otorhinolaryngologyGeneral DentistryOral Medicine and PathologyBonesbusiness.industry030206 dentistryFlorid cemento-osseous dysplasiamusculoskeletal systemmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Fibrous dysplasia of bonestomatognathic diseasesEstudi de casosDysplasiaUNESCO::CIENCIAS MÉDICASRadiologyCase studiesmedicine.symptombusinessGigantiform cementoma
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A rare form of spondylometaphyseal dysplasia-type A4

1998

We present 2 cases of a previously apparently unreported spondylo-metaphyseal dysplasia comprising dwarfism, severe metaphyseal changes, ovoid vertebrae and mild platyspondyly with anterior tonguing of the vertebral bodies. The inheritance may be autosomal recessive.

musculoskeletal diseasesmedicine.medical_specialtybusiness.industryDwarfismOvoid vertebraeAnatomymusculoskeletal systemmedicine.diseaseOsteochondrodysplasiaEndocrinologySpondylometaphyseal dysplasiaDysplasiaInternal medicinemedicinePlatyspondylysense organsMild platyspondylyCongenital diseasebusinessGenetics (clinical)American Journal of Medical Genetics
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Expression of p63, p53 and ki-67 in patients with cervical intraepithelial neoplasia

2017

Objective: Cervical intraepithelial neoplasia (CIN) is a dysplastic process in cervical squamous epithelium and carries a risk of progression to cervical cancer. The aim of this study was to compare expression of three biomarkers named p53, p63 and Ki-67 in patients with various grades of cervical intraepithelial neoplasia and in a control group. Material and Method: 58 patients were enrolled in the study. Each patient underwent a colposcopy-guided biopsy of the cervix. Immunostaining for markers (p53, p63 and Ki-67) was performed on tissue samples of normal cases (n=10), CIN I (n=20), CIN II (n=14), and CIN III (n=14). Results: Our study showed a significant increase of the expression of t…

p530301 basic medicineUterine Cervical Neoplasmsurologic and male genital diseasesGastroenterology0302 clinical medicineYoung adultCervical cancerp63medicine.diagnostic_testbiologyvirus diseasesMiddle AgedImmunohistochemistryfemale genital diseases and pregnancy complicationsKoilocytesurgical procedures operativemedicine.anatomical_structure030220 oncology & carcinogenesisKi-67Disease ProgressionKi-67ImmunohistochemistryFemalelcsh:RB1-214Adultmedicine.medical_specialtyAdolescentCervical intraepithelial neoplasiaPathology and Forensic MedicineYoung Adult03 medical and health sciencesInternal medicineBiopsyBiomarkers Tumorlcsh:PathologymedicineHumansneoplasmsCervixCervical intraepithelial neoplasiabusiness.industryMembrane ProteinsUterine Cervical Dysplasiamedicine.diseaseKi-67 Antigen030104 developmental biologybiology.proteinTumor Suppressor Protein p53businessTurkish Journal of Pathology
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Predictive value of p53, Ki67 and TLR5 in neoplastic progression of Barrett’s esophagus: a matched case–control study

2022

Abstract Barrett’s esophagus progresses to high-grade dysplasia or cancer along the well-established metaplasia-dysplasia-adenocarcinoma sequence. The aim of this study was to evaluate the value of p53, Ki67, and toll-like receptor 5 (TLR5) in prediction of malignant progression of Barrett’s metaplasia and low-grade dysplasia. This was a retrospective matched case–control study based on Northern and Central Finland population. Patients diagnosed with esophageal high-grade dysplasia or adenocarcinoma were included. From these patients, all previous endoscopy samples were obtained along with original diagnostic HE-slides and clinical data. Age- and sex-matched patients with non-progressing Ba…

p53Esophageal NeoplasmsbiomarkkeritAdenocarcinomaPathology and Forensic MedicineimmunohistokemiaBarrett EsophagusHumansBarrett’s esophagusTLR5Molecular BiologyRetrospective StudiesMetaplasiaSurveillanceCell BiologyGeneral MedicineImmunohistochemistrydigestive system diseasesToll-Like Receptor 5antigeenitKi-67 AntigenDysplasia markerCase-Control StudiesproteiinitEsophageal adenocarcinomatarkkailuTumor Suppressor Protein p53ruokatorvisyöpäKi67Virchows Archiv
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Mutations in p53 Gene Exons in a Sample from the South of Spain in Oral Cancer

2021

[Background+ Cancer is a genetic disease caused by mutations in DNA and epigenetic alterations that control gene expression. The majority of epidermoid carcinomas develop within the fields of epithelial genetic alterations. The mechanisms underlying tumorigenesis of epidermoid carcinoma are as yet unknown; therefore, precise identification of the risk factors is needed.

p53Geneticseducation.field_of_studyOral Medicine and PathologyResearchOral cancerPopulationExonCancerBiologymedicine.diseasemedicine.disease_causeChromosome 17 (human)ExonEpidermoid carcinomaDysplasiamedicineeducationCarcinogenesisGeneral DentistryGeneMutationsUNESCO:CIENCIAS MÉDICAS
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Septo-optic dysplasia and schizencephaly: a case report

2012

Introduction: Septo-optic dysplasia (SOD) is an uncommon developmental disorder involving variable midline brain structures, characterized by optic nerve hypoplasia, dysgenesis of septum pellucidum and pituitary- hypothalamic dysfunction with consequent endocrine deficits. The association of septo-optic dysplasia and cortical dysplasia is described as septo-optic dysplasia-plus. Reports on patients with septo-optic dysplasia-plus have been rare. Other distinct features, which occur especially when cerebral cortical abnormalities are also present (SOD- plus), consist of significant generalized developmental delay and/or spastic motor deficits. Methods: We report a 10-year-old boy with septo-…

schizencephalySepto-optic dysplasiaSettore MED/39 - Neuropsichiatria Infantile
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“Cola u’ Nanu”: an early nineteenth century case of disproportionate small stature

2022

This report considers Cola “u’ Nanu” (Cola the Dwarf) (Fig. 1) who was depicted in 1840 by the famous nineteenth century Sicilian painter Michele Panebianco (1806–1873).

short stature Dwarfism Genetic mutation DysplasiaArt and historyEndocrinologyEndocrinology Diabetes and MetabolismMutationHumansDwarfismSettore BIO/08 - AntropologiaSicilyJournal of Endocrinological Investigation
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Transformation of proliferative verrucous leukoplakia to oral carcinoma: a ten years follow-up

2004

Los autores presentan un caso de leucoplasia verrugosa proliferativa (LVP) en varón de 78 años de edad. Fue inicialmente presentado como un caso de leucoplasia en lengua pero un estudio microscópico en 1991 reveló la presencia de displasia epitelial leve. Tras 5 años de seguimiento, la lesión sufrió cambios de tamaño y localización y tuvo comportamiento recidivante. En 1996, un área eritematosa granular e indurada que apareció en lengua resultó ser un carcinoma de células escamosas microinvasivo cuando se estudió microscópicamente. Tras una revisión del comportamiento clinicopatológico de esta entidad, los autores concluyeron que se trataba de una leucoplasia verrugosa proliferativa, cuyo d…

squamous cell carcinomaMaleDysplasiamalignant transformationTime FactorsreviewOdontologíapapilomatosishistologycarcinoma de células escamosasclinical examinationEpithelial hyperplasiacase reportfollow upHumanshumandisplasiaPapillomatosisAgedLeucoplasia verrugosa proliferativa:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludproliferative verrucous leukoplakiaCell Transformation Neoplasticepithelium hyperplasialeukoplakiamouth carcinomaUNESCO::CIENCIAS MÉDICASCarcinoma Squamous Cellhiperplasia epitelialMouth NeoplasmsLeukoplakia OralFollow-Up Studies
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Florid cemento-osseous dysplasia: A case report

2007

Cemento-osseous dysplasias are a group of disorders known to originate from periodontal ligament tissues and involve, essentially, the same pathological process. They are usually classified, depending on their extent and radiographic appearances, into three main groups: periapical (surrounds the periapical region of teeth and are bilateral), florid (sclerotic symmetrical masses) and focal (single lesion) cemental dysplasias. Florid cemento-osseous dysplasia clearly appears to be a form of bone and cemental dysplasia that is limited to jaws. Patients do not have laboratory or radiologic evidence of bone disease in other parts of the skeleton. For the asymptomatic patient, the best management…

stomatognathic diseasesgigantiform cementomastomatognathic systemUNESCO::CIENCIAS MÉDICASFlorid cemento-osseous dysplasiafamilial multiple cementomas:CIENCIAS MÉDICAS [UNESCO]
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Regional odontodysplasia of the deciduous and permanent teeth associated with eruption disorders: A case report

2008

WOS: 000259667500007 PubMed: 18758400 Regional odontodysplasia (RO) is an unusual, non-hereditary anomaly of the dental hard tissues with characteristic clinical, radiographic and histological findings. Clinically, RO affects the primary and permanent dentition in the maxilla and mandible or both jaws. Radiographically, there is a lack of contrast between the enamel dentin, both of which are less radiopaque than unaffected counterparts. Additionally, enamel and dentin layers are thin, giving the teeth a "ghost-like" appearance. Histologically, areas of hypocalcified enamel are visible and enamel prisms appear irregular in direction. Coronal dentin is fibrous, consisting of clefts and a redu…

stomatognathic diseasesstomatognathic systemregional odontodysplasiaUNESCO::CIENCIAS MÉDICAS:CIENCIAS MÉDICAS [UNESCO]ghost teeth
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