Search results for "aplasia"

showing 10 items of 129 documents

Acquired elastotic hemangioma-like changes and eccrine sweat duct squamous metaplasia in lichen simplex chronicus/prurigo nodularis-like lesions of t…

2017

Background The so-called acquired elastotic hemangioma (AEH) represents a peculiar vascular lesion affecting the sun-damaged skin of the extensor surface of the forearms or the lateral aspect of the neck of middle-aged or elderly women. Methods This is a clinicopathological and immunohistochemical study of a series of 6 lesions located on the knee or elbow showing epithelial features of lichen simplex chronicus (LSC)/prurigo nodularis (PN) with a marked subepidermal vascular proliferation closely resembling AEH. Results Microscopically, all cases of cutaneous lesions showed epithelial features of LSC/PN, that is compact hyperkeratosis with focal parakeratosis, irregular acanthosis, prominen…

Pathologymedicine.medical_specialtyHistologyHypergranulosisbusiness.industryElbowAcanthosisDermatologyHyperplasiamedicine.diseaseSquamous metaplasiaPathology and Forensic MedicineHemangioma030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicinemedicine.anatomical_structure030220 oncology & carcinogenesismedicinebusinessDuct (anatomy)Prurigo nodularisJournal of cutaneous pathology
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Hysteroscopic Management of Endometrial Osseous Metaplasia Mimicking a Foreign Body.

2021

Pathologymedicine.medical_specialtyMetaplasiabusiness.industryOssification HeterotopicObstetrics and GynecologyHysteroscopymedicine.diseaseForeign BodiesEndometriumPregnancymedicineHumansFemaleOsseous metaplasiaForeign bodybusinessJournal of minimally invasive gynecology
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Metastasizing anaplastic ependymoma in an adult. Chromosomal imbalances, metabolic and gene expression profiles

2009

Pathologymedicine.medical_specialtyMutationHistologyGeneral MedicineIn situ hybridizationBiologymedicine.disease_causePathology and Forensic MedicineAnaplastic EpendymomaGene expression profilingGene expressionmedicinemedicine.symptomGeneAnaplasiaHistopathology
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Necrotizing sialometaplasia of the tonsillar pillar. An unusual case

2021

Necrotizing Sialometaplasia (NS) is a rare, benign, self-limited, inflammatory and necrotizing reaction of the salivary glandular tissue. Due to the clinical picture (a painful ulcer with well-defined edges), and histopathological characteristics (nuclear and cellular pleomorphism of ductal cells) NS can mimic a malignant lesion. The correct diagnosis is important because NS shows a spontaneous resolution and therefore no further treatment is needed. We report a very unusual case of spontaneous and recurrent NS located on the anterior tonsillar pillar in a 43-year old man, which clinically mimics a malignant lesion. The clinician should be aware to include NS in the differential diagnosis o…

Pathologymedicine.medical_specialtyOral Medicine and PathologyUnusual caseNecrotizing sialometaplasiaSalivary glandSoft palatebusiness.industryAnterior tonsillar pillarCase ReportBenign lesionmedicine.diseasemedicine.anatomical_structuremedicineDifferential diagnosisbusinessGeneral DentistryUNESCO:CIENCIAS MÉDICASTonsillar Pillar
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Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal p…

1998

We present the findings and clinical course of a Caucasian woman (now age 23½) who has been treated since early childhood for a previously undescribed syndrome of painful osteocartilaginous metaplasia of long bone metaphyses and painful distal phalangeal osteolysis and soft tissue swelling. Despite extensive evaluations and attempts at effective treatment, the cause and pathogenesis of her unique musculoskeletal disorder remain elusive. Am. J. Med. Genet. 80:187–195, 1998. © 1998 Wiley-Liss, Inc.

Pathologymedicine.medical_specialtyOsteolysisbusiness.industryLong boneCoxa varaSoft tissueAnatomyPhalanxmedicine.diseaseOsteochondrodysplasiamedicine.anatomical_structureSpondylometaphyseal dysplasiaMetaplasiamedicinemedicine.symptombusinessGenetics (clinical)American Journal of Medical Genetics
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Role of chronic exposure to cigarette smoke on endoglin/CD105 expression in airway epithelium

2015

Dysregulation of airway epithelium function related to cigarette smoke exposure plays an important role in the pathophysiology of COPD and is associated to tissue damage and disease severity. CD105 is a component of the receptor complex of TGF-β, a pleiotropic cytokine involved in cellular proliferation, differentiation and migration. CD105 regulates the expression of different components of the extracellular matrix suggesting a role of CD105 in cellular transmigration and remodeling processes. The aim of the present study was to investigate the expression of endoglin/CD105 in airway epithelium of COPD patients and its involvement in tissue remodeling and COPD progression. We evaluated the …

Pathologymedicine.medical_specialtyReceptor complexCOPDbusiness.industrymedicine.medical_treatmentInflammationEndoglinmedicine.diseaseSquamous metaplasiaEpitheliumrespiratory tract diseasesmedicine.anatomical_structureCytokinemedicineRespiratory epitheliummedicine.symptombusiness3.3 Mechanisms of Lung Injury and Repair
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Scanning electron microscopy of the cervix uteri.

1974

Scanning electron microscopy has been used in the study of five cases of the cervix uteri: two normal cases; one case of indirect metaplasia; one case of carcinoma in situ whose colposcopic examination showed an erosio vera surrounded by leucoplasia, mosaic, base, and an area of atipic transformation zone and one case of invasive carcinoma.

Pathologymedicine.medical_specialtyScanning electron microscopeBiopsyUterine Cervical NeoplasmsCervix Uterilaw.inventionlawMetaplasiamedicineCarcinomaHumansCervixUterine DiseasesMetaplasiaInvasive carcinomabusiness.industryCarcinoma in situCarcinomaObstetrics and GynecologyEpithelial CellsGeneral Medicinemedicine.diseasemedicine.anatomical_structureColposcopyCarcinoma Squamous CellMicroscopy Electron ScanningFemalemedicine.symptomElectron microscopeTransformation zonebusinessCarcinoma in SituArchiv fur Gynakologie
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KLEIP Deficiency in Mice Causes Progressive Corneal Neovascular Dystrophy

2012

PURPOSE. The BTB-kelch protein KLEIP/KLHL20 is an actin binding protein that regulates cell-cell contact formation and cell migration. The aim of our study was to characterize KLEIP’s function in ocular health and disease in mice. METHODS. KLEIP -/- mice were generated, and corneas were examined histologically and stained for keratin-1, loricrin, keratin-12, keratin-14, CD31, LYVE-1, F4/80, E-cadherin, and Ki67. Corneal abrasions were performed after eyelid opening. RESULTS. Corneas of KLEIP þ/þ and KLEIP -/- mice were indistinguishable at birth. After eyelid opening corneal epithelial hyperplasia started to manifest in KLEIP -/- mice, showing a progressive epithelial metaplasia leading to …

Pathologymedicine.medical_specialtyStromal cellGenotypeMice TransgenicCorneal dystrophyReal-Time Polymerase Chain ReactionCorneaMiceCorneal OpacityCorneamedicineAnimalsCorneal NeovascularizationRNA MessengerAdaptor Proteins Signal TransducingCorneal epitheliumintegumentary systembusiness.industryDystrophymedicine.diseaseeye diseasesEpitheliumMice Inbred C57BLDisease Models Animalmedicine.anatomical_structureGene Expression RegulationDisease ProgressionEpithelial MetaplasiaLoricrinsense organsCarrier ProteinsbusinessInvestigative Opthalmology & Visual Science
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Bilateral agenesis/aplasia of the lungs: report of a second case in the offspring of one woman.

1995

Congenital absence of both lungs is an extremely rare malformation in humans and is thought to occur sporadically. We report the second case of congenital absence of both lungs in the offspring of one woman. In neither case, one female baby (born at term) and one aborted female fetus (21 weeks of gestation), were anomalies or malformations of other organ systems observed. The karyotype of the aborted fetus was 46,XX. To our knowledge, this is the first report describing bilateral pulmonary agenesis in two offspring of one mother. The repetition of virtually the same isolated abnormality with no other malformations supports the hypothesis that it could be caused by a genetic disorder. Other …

Pediatricsmedicine.medical_specialtyLungbusiness.industryOffspringAborted FetusAplasiamedicine.diseasePathology and Forensic MedicineSurgeryFetal DiseasesParitymedicine.anatomical_structurePregnancyAgenesisKaryotypingPediatrics Perinatology and Child HealthEtiologyMedicineGestationHumansFemaleAbnormalitybusinessLungPediatric pathologylaboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association
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Mast cell-derived tumour necrosis factor is essential for allergic airway disease

2007

Mast cells are thought to contribute to allergic airway disease. However, the role of mast cell-produced mediators, such as tumour necrosis factor (TNF), for the development of allergic airway disease is unclear. In order to define the role of mast cells in acute allergic airway disease two strains of mast cell-deficient mice (Kit W/Wv and Kit W-sh/W-sh ) were studied. Compared with their wild-type littermates, Kit W/Wv and Kit W-sh/W-sh mice developed significantly lower airway responsiveness to methacholine and less airway inflammation and goblet cell metaplasia, following sensitisation in the absence of adjuvant and airway challenge. Transfer of bone marrow-derived mast cells (BMMCs) fro…

Pulmonary and Respiratory MedicineAllergyPathologymedicine.medical_specialtyNecrosisInflammationMiceMetaplasiamedicineAnimalsMast CellsInflammationMice KnockoutGoblet cellTumor Necrosis Factor-alphabusiness.industryAllergensrespiratory systemmedicine.diseaseMast cellAsthmarespiratory tract diseasesDisease Models Animalmedicine.anatomical_structureImmunologyImmunizationTumor necrosis factor alphaGoblet CellsBronchial Hyperreactivitymedicine.symptomAirwaybusinessEuropean Respiratory Journal
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