Search results for "Prognosi"

showing 10 items of 2082 documents

Different immunophenotypical apoptotic profiles characterise megakaryocytes of essential thrombocythaemia and primary myelofibrosis.

2009

Aims: Essential thrombocythaemia (ET) and primary myelofibrosis (PMF) share some clinical and pathological features, but show different biological behaviour and prognosis. The latest contributions to understanding the nature of these disorders have focused on bone marrow microenvironment remodelling and proliferative stress, recognising megakaryocytes (MKCs) as “key-cells”. The aim of this study was to investigate the apoptotic profile of ET and PMF MKCs in order to further characterise the biology of these disorders. Methods: Bone marrow biopsy samples from 30 patients with ET, and 30 patients with PMF, were immunophenotypically studied for the expression of pro-apoptotic (Fas, Fas-L, Bax,…

AdultMalePathologymedicine.medical_specialtyBiopsyIDIOPATHIC MYELOFIBROSISApoptosisPOLYCYTHEMIA-VERASettore MED/08 - Anatomia PatologicaBiologyPathology and Forensic MedicineImmunophenotypingImmunophenotypingMegakaryocyteBone MarrowmedicineIn Situ Nick-End LabelingHumansTelomerase reverse transcriptaseMyelofibrosisMOLECULAR PERSPECTIVEAgedAged 80 and overTUNEL assayEssential thrombocythemiaC-MPLMUTATION STATUSGeneral MedicineMiddle Agedmedicine.diseasePrognosismedicine.anatomical_structureCHRONIC MYELOPROLIFERATIVE DISORDERSCELL-DEATHApoptosisPrimary MyelofibrosisRISK-FACTORSCancer researchBONE-MARROW ANGIOGENESISMYELOID METAPLASIAFemaleBone marrowMegakaryocytesThrombocythemia EssentialJournal of clinical pathology
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Quantitative DNA measurements in malignant and benign lesions of the upper aerodigestive tract.

1992

Thirty-six patients underwent biopsy of clinically suspicious lesions of the mucosa of the upper aerodigestive tract. The biopsy material was evaluated histologically and cytologic smears out of the same lesion underwent quantitative DNA analysis using a numerical index derived from the single cell DNA content. In 30 patients, histologically diagnosed squamous cell cancer was confirmed by DNA analysis with the malignancy grade correlating with the morphologic differentiation of the tumor. Six lesions were histologically benign: i.e. dysplasia (n = 3), hyperplasia (n = 2) and chronic inflammation (n = 1). DNA analysis confirmed the benign nature in 4 cases, but in 2 cases of dysplasia, a dia…

AdultMalePathologymedicine.medical_specialtyBiopsyMalignancyDigestive System NeoplasmsModels BiologicalLesionCytologyBiopsymedicineHumansAgedmedicine.diagnostic_testbusiness.industryHistologyDNAHyperplasiaMiddle Agedmedicine.diseaseFlow CytometryPrognosisUpper aerodigestive tractOtorhinolaryngologyDysplasiaCarcinoma Squamous CellFemalemedicine.symptombusinessORL; journal for oto-rhino-laryngology and its related specialties
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Chromophobe cell renal carcinoma and its variants--a report on 32 cases.

1988

This paper reports on 32 chromophobe cell renal carcinomas observed in 697 renal cell cancers (RCC) of adults (peak in the sixth decade of life). The chromophobe cell-type differs from other types of RCC macroscopically, the cut-surface being predominantly of grey-beige colour. Histologically, there are two variants: one is the typical (light) variant (n = 22) and the other is eosinophilic (n = 10). Both variants have in common (a) reaction of the cytoplasm with Hale's acid iron colloid; (b) electron microscopic detection of cytoplasmic microvesicles (150-300 nm), frequently with 'inner vesicles', and (c) low glycogen content in comparison with the clear cell carcinoma. Immunocytochemical i…

AdultMalePathologymedicine.medical_specialtyChromophobe Renal Cell CarcinomaIntermediate FilamentsVimentinChromophobe cellBiologyurologic and male genital diseasesPathology and Forensic MedicineRenal cell carcinomamedicineCarcinomaHumansVimentinIntermediate filamentGrading (tumors)Carcinoma Renal CellAgedStaining and LabelingMiddle Agedmedicine.diseasePrognosisKidney NeoplasmsMicroscopy ElectronClear cell carcinomaVacuolesbiology.proteinEosine Yellowish-(YS)KeratinsFemaleGlycogenThe Journal of pathology
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DNA image cytometry

1992

In 68 patients the DNA content of tumor cells was measured by image cytometry after resection of the rectum because of cancer. In the DNA histogram a differentiation between diploid (n = 19), polyploid (n = 24), hypotriploid (n = 17), and hypertriploid (n = 8) tumors was possible. The best relapse-free survival time was found in patients with diploid tumors. The prognosis worsened from polyploid to hypotriploid and was worse in hypertriploid tumors. Testing for a prognostic advantage of diploid over aneuploid tumors without adjustment for additional factors simply by means of the log-rank statistic gave a (one-sided) P of 0.1013. In a multivariate analysis the degree of differentiation turn…

AdultMalePathologymedicine.medical_specialtyColorectal cancerRectumPolyploidRisk FactorsSurgical oncologymedicineHumansComputer SimulationDNA Image CytometryAgedAged 80 and overAnalysis of VariancePloidiesRectal Neoplasmsbusiness.industryGastroenterologyCancerDNA NeoplasmGeneral MedicineMiddle AgedPrognosismedicine.diseasemedicine.anatomical_structureCancer researchImage CytometryFemaleCytophotometryNeoplasm Recurrence LocalbusinessCytometryDiseases of the Colon & Rectum
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Confocal Endomicroscopy Identifies Loss of Local Barrier Function in the Duodenum of Patients with Crohnʼs Disease and Ulcerative Colitis

2014

Background: Increased cell shedding with gap formation and local barrier dysfunction can be identified endomicroscopically in the terminal ileum of patients with inflammatory bowel disease. We aim to evaluate whether these changes are also present in the duodenum of patients with inflammatory bowel disease. Methods: Fifteen patients with Crohn's disease (CD), 10 patients with ulcerative colitis (UC), and 10 controls underwent fluorescein-aided confocal laser endomicroscopy (CLE). CLE was performed on macroscopically normal antral and duodenal (D1, D2, D3, D4) mucosa. Representative CLE images were prospectively analyzed. Images were scored for the number of epithelial gaps, cell shedding, a…

AdultMalePathologymedicine.medical_specialtyDuodenumInflammatory bowel diseaseGastroenterologyEndoscopy GastrointestinalEpithelial DamageYoung AdultCrohn DiseaseDuodenitisRisk FactorsInternal medicinemedicineEndomicroscopyHumansImmunology and AllergyProspective StudiesColitisAgedFluorescent DyesCrohn's diseaseMicroscopy ConfocalDuodenitisbusiness.industryGastroenterologyMiddle AgedPrognosismedicine.diseaseUlcerative colitismedicine.anatomical_structureCase-Control StudiesDuodenumColitis UlcerativeFemaleFluoresceinbusinessFollow-Up StudiesInflammatory Bowel Diseases
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Electrophysiological and MRI findings in 2 patients with Listeria rhombencephalitis.

1997

AdultMalePathologymedicine.medical_specialtyElectrodiagnosisMeningitis Listeriamedicine.disease_causeCentral nervous system diseaseListeria monocytogenesmedicineEvoked Potentials Auditory Brain StemHumansListeriosismedicine.diagnostic_testbiologyBlinkingReflex Abnormalbusiness.industrymedicine.diseasebiology.organism_classificationPrognosisMagnetic Resonance ImagingElectrophysiologyNeurologyListeriaEncephalitisFemaleNeurology (clinical)businessMri findingsEncephalitisBrain StemEuropean neurology
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CXCR3 chemokine receptor immunoreactivity in primary cutaneous malignant melanoma: correlation with clinicopathological prognostic factors.

2007

A role for CXCR3, the receptor for chemokines Mig, IP-10 and interferon-inducible T cell alpha-chemoattractant, in tumour cell migration during melanoma progression has been proposed.To analyse CXCR3 expression in primary cutaneous malignant melanomas and its comparison with clinicopathological and prognostic factors.A retrospective immunohistochemical study was carried out on formalin-fixed paraffin-wax-embedded sections from 82 patients with primary invasive cutaneous melanomas, with a monoclonal antibody to CXCR3 (clone 49801.111; RD Systems). Immunoreactivity was semiquantitatively evaluated: labelling intensity (0, absent; 1, weak; 2, moderate; 3, strong) multiplied by the percentage o…

AdultMalePathologymedicine.medical_specialtyReceptors CXCR3Skin NeoplasmsCXCR3Pathology and Forensic MedicineImmunoenzyme TechniquesmedicineBiomarkers TumorHumansNeoplasm InvasivenessLymph nodeMelanomaAgedRetrospective StudiesAged 80 and overUnivariate analysisbusiness.industryMelanomaGeneral MedicineMiddle Agedmedicine.diseasePrognosisSurvival AnalysisNeoplasm Proteinsmedicine.anatomical_structureLymphatic MetastasisCutaneous melanomaDisease ProgressionImmunohistochemistryFemaleReceptors ChemokineOriginal ArticleSkin cancerbusinessImmunostainingJournal of clinical pathology
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Evaluation of prognostic factors and their capacity to predict biological behavior in gastrointestinal stromal tumors.

2011

Gastrointestinal stromal tumors (GISTs) are c-KIT-signaling-driven mesenchymal tumors of the human digestive tract, many of which have c-KIT or PDGFRα activating mutations. The authors studied the immunohistochemical markers, c-KIT and PDGFRα mutations, in GISTs and their association with the clinicopathological and clinical follow-up in 145 GISTs. Tumors were located mainly in the stomach, the median tumor size being 7.5 cm. The mitotic index was ≤5 mitoses per 50 high-power fields in 61% of cases, 96% expressed CD117, and c-KIT or PDGFRα mutations were detected in 68% of cases. The median follow-up of the series was 52 months (range = 1 to 244.9 months). Tumor size, cell morphology, mito…

AdultMalePathologymedicine.medical_specialtyStromal cellMitotic indexReceptor Platelet-Derived Growth Factor alphaGastrointestinal Stromal Tumorsmedicine.disease_causeCell morphologyDisease-Free SurvivalPathology and Forensic MedicineYoung AdultPredictive Value of TestsStomach NeoplasmsIntestinal NeoplasmsmedicineBiomarkers TumorMitotic IndexHumansAgedAged 80 and overMutationbiologyCD117StomachMesenchymal stem cellMiddle AgedPrognosisProto-Oncogene Proteins c-kitmedicine.anatomical_structureKi-67 AntigenMutationbiology.proteinImmunohistochemistrySurgeryFemaleAnatomyInternational journal of surgical pathology
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Obesity after childhood craniopharyngioma--German multicenter study on pre-operative risk factors and quality of life.

2001

Craniopharyngiomas are tumorous embryogenic malformations. As the survival rate after craniopharyngioma is high (92 %), prognosis and quality of life (QoL) in survivors mainly depend on adverse late effects such as obesity.We analyzed 214 children and adolescents with craniopharyngioma. The records of 185 patients (86 %) were available for retrospective analysis of weight profiles and risk factors for obesity. Quality of life (QoL) was measured in 145 patients by the Fertigkeitenskala Münster/Heidelberg score (FMH) and in 77 patients by PEDQOL questionnaire.Eighty-two of 185 patients (44 %) developed severe obesity (body mass index [BMI]3 SD). Obese patients were compared with 79 patients (…

AdultMalePediatricsmedicine.medical_specialtyAdolescent030209 endocrinology & metabolismWeight GainFeeding and Eating Disorders03 medical and health sciencesCraniopharyngioma0302 clinical medicineQuality of lifeRisk FactorsGermanymedicineHumansGenetic Predisposition to DiseasePituitary NeoplasmsRisk factorChildSurvival rateRetrospective Studies2. Zero hungerbusiness.industryIncidenceChildhood CraniopharyngiomaInfant NewbornInfantOdds ratiomedicine.diseasePrognosisCraniopharyngioma3. Good healthObesity MorbidAustriaChild PreschoolPediatrics Perinatology and Child HealthQuality of LifeFemalemedicine.symptombusinessWeight gainBody mass index030217 neurology & neurosurgerySwitzerlandFollow-Up StudiesKlinische Padiatrie
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The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents.

2003

Fabry disease (FD) is a debilitating progressive multisystem X-linked lysosomal storage disorder. It was generally believed that the disease affects only adult males. Through systematic pedigree analysis, we identified 35 paediatric FD patients (age 1 to 21 years, mean 12.6 years) in 25 families. Predominant signs in this cohort were: acroparesthesia, hypohidrosis, and cornea verticillata. Neurological and psychological changes, such as tinnitus, recurrent vertigo, headache, diminished level of activity, fatigue, and depression were often observed. Angiokeratoma and gastrointestinal symptoms were frequent. Some patients also showed cardiac abnormalities. Six children and adolescents (three …

AdultMalePediatricsmedicine.medical_specialtyAdolescentDiseaseRisk AssessmentSeverity of Illness IndexCohort StudiesAge DistributionSeverity of illnessmedicineHumansCornea verticillataGenetic Predisposition to DiseaseSex DistributionChildDepression (differential diagnoses)business.industryIncidenceEnzyme replacement therapymedicine.diseasePrognosisFabry diseaseHealth SurveysAngiokeratomaSurgeryEuropePhenotypeChild PreschoolPediatrics Perinatology and Child HealthFabry DiseaseFemalemedicine.symptombusinessCohort studyEuropean journal of pediatrics
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