Search results for " Dysplasia"

showing 10 items of 206 documents

Oculoectodermal syndrome: Report of a new case with a broad clinical spectrum

2014

Oculoectodermal syndrome (OMIM 600268) is rare and characterized by aplasia cutis congenita, epibulbar dermoids, and other abnormalities. We report herein on a newly recognized patient with oculoectodermal syndrome, which is the 19th reported patient with OES. The boy aged six years demonstrated a broad clinical spectrum of this condition, including aplasia cutis congenita, epibulbar dermoids, hyperkeratotic papule, mildly enlarged cisterna magna, and an enlarged fluid space in the quadrigeminal cistern, suggesting a cyst. He also manifested anomalies not reported associated with this disorder, including systematized epidermal nevus following Blaschko's lines, hypopigmented skin lesions, an…

Malemusculoskeletal diseasescongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyAplasia cutis congenitaHypopigmented skin lesionsEctodermal DysplasiaOculoectodermal syndromeGeneticsmedicineHumansCystGenetics (clinical)Dermoid CystSkinHyperkeratotic papuleHypopigmentationSystematized epidermal nevusbusiness.industryEpibulbar dermoidsBrainmedicine.diseaseMagnetic Resonance ImagingDermatologyEnlarged cisterna magnaPhenotypeChild Preschoolmedicine.symptombusinessAmerican Journal of Medical Genetics Part A
researchProduct

Rare association of human herpesvirus 6 DNA with human papillomavirus DNA in cervical smears of women with normal and abnormal cytologies.

1996

We investigated by nested PCR the possible association of human herpesvirus 6 (HHV-6) and human papillomavirus (HPV) genomes in the cervixes of 109 women with normal and abnormal cytological smears. HPV DNA was detected in 8.33% of 24 women with normal cytologies and in 41.1% of 85 women with abnormal cytologies; the proportion of HPV DNA was directly related to the severity of the lesions. HHV-6 DNA was found in only one patient, who had a cytological pattern of koilocytosis. The HHV-6 genome was classified by restriction enzyme analysis as variant B. The study indicates that detection of the HHV-6 genome in the cervixes of women with a wide spectrum of gynecological complaints is a rare e…

Microbiology (medical)AdultPathologymedicine.medical_specialtyvirusesHerpesvirus 6 HumanUterine Cervical NeoplasmsCervix UteriBiologyCervical intraepithelial neoplasiamedicine.disease_causePolymerase Chain ReactionHerpesviridaelaw.inventionlawmedicineHumansPapillomaviridaePapillomaviridaePolymerase chain reactionCervical cancerVaginal SmearsCocarcinogenesisvirus diseasesMiddle Agedmedicine.diseasebiology.organism_classificationUterine Cervical DysplasiaVirologyKoilocyteDNA ViralHuman herpesvirus 6FemaleNested polymerase chain reactionResearch ArticleJournal of clinical microbiology
researchProduct

PD-L1 and PD-1 expression in thyroid follicular epithelial dysplasia : Hashimoto thyroiditis related atypia and potential papillary carcinoma precurs…

2022

Programmed cell death ligand (PD-L1)/PD-1 expression has been studied in a variety of cancers and blockage of PD-L1/PD-1 pathway is a cornerstone of immunotherapy. We studied PD-L1/PD-1 immunohistochemical expression in 47 thyroid gland specimens in groups of (1) Hashimoto thyroiditis (HT) only; (2) HT and follicular epithelial dysplasia (FED); and (3) HT, FED, and papillary thyroid carcinoma (PTC). PD-1 positivity was found in immune cells, namely in lymphocytes, macrophages, and plasma cells with mean values for lymphocytes and macrophages 9% in HT group, 4% in FED group, and 4% in PTC group. PD-L1 positivity was identified in both immune cells and in the normal epithelial cells. In the H…

Microbiology (medical)PD-L1Hashimoto thyroiditissyövän esiasteetthyroid glandendocrine system diseasesdysplasiatProgrammed Cell Death 1 ReceptorkilpirauhanenGeneral MedicineHashimoto Disease3121 Internal medicineB7-H1 AntigenCarcinoma PapillarykarsinoomatPathology and Forensic MedicineThyroid Cancer PapillaryimmuunijärjestelmäPD-1papillary thyroid carcinomaImmunology and AllergyHumansfollicular epithelial dysplasiaThyroid Neoplasms3111 Biomedicine
researchProduct

Expression profile of components of the β-catenin destruction complex in oral dysplasia and oral cancer

2021

Background Oral cancer represents the sixth most common cancer in the world and is associated with 40-50% survival at 5 years. Within oral malignancies, oral squamous cell carcinoma (OSCC) is commonly preceded by potentially malignant lesions, which, according to histopathological criteria, are referred to as oral dysplasia and their diagnosis are associated with higher rates of malignant transformation towards cancer. We recently reported that aberrant activation of the Wnt/β‑catenin pathway is due to overexpression of Wnt ligands in oral dysplasia. However, the expression of other regulators of this pathway, namely components of the β-catenin destruction complex has not been explored in o…

Mild DysplasiaAdenomatous polyposis coliMalignant transformationmalignantOral Cancer and Potentially malignant disordersHumansMedicineWnt Signaling PathwayGeneral DentistryGSK3Bbeta CateninUNESCO:CIENCIAS MÉDICASOral DysplasiaAxin Signaling ComplexGlycogen Synthase Kinase 3 betabiologySquamous Cell Carcinoma of Head and Neckbusiness.industryResearchWnt signaling pathwayCancerfloor of the mouthmedicine.diseasestomatognathic diseasesOtorhinolaryngologyCateninCarcinoma Squamous Cellbiology.proteinCancer researchMouth NeoplasmsepidemiologySurgerybenignbusinessMedicina Oral Patología Oral y Cirugia Bucal
researchProduct

The Artek cup for total hip replacement of dysplastic hip joints.

2003

One specific difficulty in total hip replacement for developmental dysplasia of the hip is a shallow acetabulum with a short anteroposterior diameter. In a prospective cohort study we investigated the short-term results of the Artek cup, designed with a shallow outline and a height-reduced metal inlay for a large size 38 mm metal head, in a group of female patients with mild dysplasia of the hip.Fourteen consecutive patients with 17 dysplastic hip joints were included in the study. Their average age was 42 years. Fourteen hips had dysplasia Crowe grade I; 3 hips had dysplasia Crowe grade II. The femoral head centre was localized according to Pagnano in zone 1 in 3 cases, in zone 3 in 6 case…

Mild DysplasiaAdultReoperationmedicine.medical_specialtymedicine.medical_treatmentArthroplasty Replacement HipBone graftingProsthesis DesignFemoral headmedicineHumansOrthopedics and Sports MedicineHip Dislocation CongenitalOrthodonticsbusiness.industryGeneral MedicineMiddle Agedmedicine.diseaseAcetabulumArthroplastySurgeryRadiographymedicine.anatomical_structureTreatment OutcomeDysplasiaHarris Hip ScoreOrthopedic surgerySurgeryFemaleHip ProsthesisbusinessFollow-Up StudiesArchives of orthopaedic and trauma surgery
researchProduct

Analysis of cell proliferation rate in Oral Leukoplakia and Oral Squamous Cell Carcinoma

2010

Objectives: Assessment of the cell proliferation rate in tissues can be one of the markers for impending malignancy in precancers. The state of activation and the proliferation activity of the cells can be assessed by the frequency of silver stained Nucleolar Organiser regions (AgNOR) within the nuclei which is significantly higher in malignant cells. The present study was carried out to analyze the distribution of the AgNOR in oral leukoplakia (OL) and oral squamous cell carcinoma (OSCC), and in their various histological grades, and to assess if the AgNOR distribution could give information on the malignant potentiality in premalignant lesions and aggressiveness of the malignant lesions. …

Mild DysplasiaPathologymedicine.medical_specialtySilver Staining MethodH&E stainOdontologíaBiology:CIENCIAS MÉDICAS [UNESCO]Malignancymedicine.diseaseCiencias de la saludOral leukoplakiastomatognathic diseasesDysplasiaProliferation rateUNESCO::CIENCIAS MÉDICASmedicineGeneral DentistryModerate DysplasiaJournal of Clinical and Experimental Dentistry
researchProduct

Immunohistochemical/histochemical double staining method in the study of the columnar metaplasia of the oesophagus

2014

Intestinal metaplasia in Barrett’s oesophagus (BO) represents an important risk factor for oesophageal adenocarcinoma. Instead, few and controversial data are reported about the progression risk of columnar-lined oesophagus without intestinal metaplasia (CLO), posing an issue about its clinical management. The aim was to evaluate if some immunophenotypic changes were present in CLO independently of the presence of the goblet cells. We studied a series of oesophageal biopsies from patients with endoscopic finding of columnar metaplasia, by performing some immunohistochemical stainings (CK7, p53, AuroraA) combined with histochemistry (Alcian-blue and Alcian/PAS), with the aim of simultaneousl…

Mild Dysplasiap53MalePathologymedicine.medical_specialtyHistologyEsophageal NeoplasmsBiophysicsSettore MED/08 - Anatomia PatologicaBiologyAdenocarcinomadigestive systemBarrett EsophagusEsophagusAntigenMetaplasiamedicineHumansEsophaguslcsh:QH301-705.5Retrospective StudiesMetaplasiaStaining and LabelingBrief ReportBarrett’s oesophagusIntestinal metaplasiaCell Biologymedicine.diseaseImmunohistochemistryEpitheliumdigestive system diseasesBarrett’s oesophagus columnar-lined oesophagus p53 Aurora A kinasemedicine.anatomical_structureBarrett’s oesophagus columnar-lined oesophagus p53 Aurora A kinase.lcsh:Biology (General)columnar-lined oesophagusAdenocarcinomaImmunohistochemistryAurora A kinaseFemaleGoblet Cellsmedicine.symptomEuropean Journal of Histochemistry
researchProduct

The frequency of non-syndromic distomolar teeth in a Greek population sample?

2015

Background: To investigate the frequency of non-syndromic distomolars in a Greek population sample. Material and Methods: The study population of this retrospective study consisted of 859 Orthopantomograms (OPGs) of 425 male and 434 female patients, attended the Department of Oral Diagnosis and Radiology, Dental School of Athens seeking for treatment. The OPGs were taken as a part of the patients treatment planning. Patients’ mean age was 33.57 years. Exclusion criteria from this study was cleft lip ± palate and diseases associated with systemic conditions and syndromes (such as cleidocranial dysplasia and Gardner syndrome). OPGs were only included in the study if at least one 3 rd molar wa…

MolarCleidocranial Dysplasiabusiness.industryResearchMandibleDentistryOdontología:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseBioinformaticsCiencias de la saludstomatognathic systemMaxillaUNESCO::CIENCIAS MÉDICASmedicinePopulation studySupernumeraryMalocclusionOral Surgery10. No inequalitybusinessGeneral DentistryPulp necrosisJournal of clinical and experimental dentistry
researchProduct

Actinic cheilitis and lip squamous cell carcinoma : literature review and new data from Brazil

2018

Background To investigate the prevalence of malignant and potentially malignant lesions of the lip in an oral pathology service and to compare these data with a literature review. Material and methods A total of 3173 biopsy reports and histopathological records were analyzed. Cases with a histological diagnosis of actinic cheilitis (AC) with or without epithelial dysplasia, in situ carcinoma, or lip squamous cell carcinoma (LSCC) were included. A comprehensive literature review was conducted to investigate the prevalence of AC and/or LSCC. Results 124 cases (3.91%) were included, 75 (60.5%) had some degree of epithelial dysplasia and 31 (25.0%) were LSCC. Clinically, most of the lesions wer…

Mouth neoplasmmedicine.medical_specialtyEpithelial dysplasiaOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryActinic cheilitis030206 dentistryReview:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseDermatologyLesion03 medical and health sciences0302 clinical medicine030220 oncology & carcinogenesisOral and maxillofacial pathologyBiopsyUNESCO::CIENCIAS MÉDICASCarcinomamedicinemedicine.symptombusinessGeneral DentistryLip Squamous Cell Carcinoma
researchProduct

Pain Phenotypes in Rare Musculoskeletal and Neuromuscular Diseases

2020

For patients diagnosed with a rare musculoskeletal or neuromuscular disease, pain may transition from acute to chronic; the latter yielding additional challenges for both patients and care providers. We assessed the present understanding of pain across a set of ten rare, noninfectious, noncancerous disorders; Osteogenesis Imperfecta, Ehlers-Danlos Syndrome, Achondroplasia, Fibrodysplasia Ossificans Progressiva, Fibrous Dysplasia/McCune-Albright Syndrome, Complex Regional Pain Syndrome, Duchenne Muscular Dystrophy, Infantile- and Late-Onset Pompe disease, Charcot-Marie-Tooth Disease, and Amyotrophic Lateral Sclerosis. Through the integration of natural history, cross-sectional, retrospective…

Neuromuscular diseaseCognitive NeuroscienceDuchenne muscular dystrophyPainDiseaseBioinformaticsArticle03 medical and health sciencesBehavioral Neuroscience0302 clinical medicinemedicineHumans0501 psychology and cognitive sciences050102 behavioral science & comparative psychologyAmyotrophic lateral sclerosisRetrospective Studiesbusiness.industryFibrous dysplasia05 social sciencesNeuromuscular Diseasesmedicine.diseaseCross-Sectional StudiesPhenotypeNeuropsychology and Physiological PsychologyComplex regional pain syndromeOsteogenesis imperfectaFibrodysplasia ossificans progressivabusiness030217 neurology & neurosurgeryNeuroscience & Biobehavioral Reviews
researchProduct