Search results for "Forensic"

showing 10 items of 1701 documents

Mitotic figure counts are significantly overestimated in resection specimens of invasive breast carcinomas.

2013

Several authors have demonstrated an increased number of mitotic figures in breast cancer resection specimen when compared with biopsy material. This has been ascribed to a sampling artifact where biopsies are (i) either too small to allow formal mitotic figure counting or (ii) not necessarily taken form the proliferating tumor periphery. Herein, we propose a different explanation for this phenomenon. Biopsy and resection material of 52 invasive ductal carcinomas was studied. We counted mitotic figures in 10 representative high power fields and quantified MIB-1 immunohistochemistry by visual estimation, counting and image analysis. We found that mitotic figures were elevated by more than th…

Pathologymedicine.medical_specialtyMitotic indexTime FactorsTissue FixationBiopsyMitosisBreast NeoplasmsBiologyPathology and Forensic MedicineBreast cancerPredictive Value of TestsBiopsyCarcinomamedicineMitotic IndexHumansNeoplasm InvasivenessMetaphaseMitosisMastectomyCell Proliferationmedicine.diagnostic_testCarcinoma Ductal BreastReproducibility of ResultsCell cyclemedicine.diseaseImmunohistochemistryKi-67 AntigenMitotic FigureLinear ModelsFemaleNeoplasm GradingModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
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Myopathology of non-infectious inflammatory myopathies - the current status.

2007

Besides the classical inflammatory myopathies (IM), dermatomyositis (DM), polymyositis, and inclusion body myositis, the much larger spectrum of IM includes focal and nodular myositis, granulomatous myositis, macrophagic myofasciitis, graft vs. host myositis, eosinophilic myositis, and other immune-associated conditions, some of them only recently described. In addition, paraneoplastic, statin-induced and critical illness myopathies have been considered immune-associated IM. Infectious, i.e., bacterial, viral, and parasitic IM are much less frequent in the northern hemisphere. In IM, muscle biopsy is an essential diagnostic procedure to initiate therapy. The myopathological spectrum encompa…

Pathologymedicine.medical_specialtyMuscle biopsymedicine.diagnostic_testMyositisbusiness.industryMacrophagic myofasciitisCell BiologyDermatomyositismedicine.diseasePolymyositisImmunohistochemistryPathology and Forensic MedicineAtrophyEosinophilicImmunologymedicineHumansInclusion body myositisbusinessMyositisPathology, research and practice
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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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Absence of p53 gene mutations in hepatocarcinomas from a Mediterranean area of Spain

1999

The incidence of p53 gene abnormalities in human hepatocellular carcinoma (HCC) varies in different geographical areas, being higher in regions where hepatitis virus infection and dietary exposure to aflatoxin B1 are the most common aetiological agents. These mutations are less frequently encountered in Europe, although some studies have reported p53 protein overexpression in up to 45% of cases analysed. We have analysed 129 tumour samples of primary malignant hepatic neoplasms recovered from paraffin blocks processed in two pathology laboratories in a Mediterranean area of Spain (Valencia and Gerona). Among 14 cases in which p53 immunohistochemistry expression proved positive, 5 stained in…

Pathologymedicine.medical_specialtyMutationTumor suppressor geneIncidence (epidemiology)Cell BiologyGeneral MedicineGene mutationBiologymedicine.diseasemedicine.disease_causePathology and Forensic MedicineMalignant transformationExonHepatocellular carcinomamedicineMolecular BiologyGeneVirchows Archiv
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Dystrophin and metalloproteinase 9 in myocardial ischemia: A post-mortem immunohistochemical study

2021

The presented study evaluated the expression of dystrophin and MMP-9 in cases of sudden cardiac death (SCD) due to coronary atherosclerotic disease (CAD) in order to analyze the characteristics and the chronology of their expression, providing evidence on the possible role in post-mortem diagnosis of myocardial ischemia. The expression of these proteins was also compared to C5b-9 complex and fibronectin expression to evaluate any differences. Two groups of CAD-related SCD, respectively group 1 with gross and/or histological evidence and group 2 with no specific histological signs of myocardial ischemia, were used. A third group formed by cases of acute mechanical asphyxiation was used as a …

Pathologymedicine.medical_specialtyMyocardial ischemiaMyocardial IschemiaCoronary Artery DiseasePathology and Forensic MedicineSudden cardiac deathDystrophin; Immunohistochemistry; MMP-9; Myocardial ischemia; Post-mortem analysis; Sudden cardiac deathDystrophinmedicineHumansMetalloproteinasebiologybusiness.industryMyocardiummedicine.diseaseImmunohistochemistryStainingFibronectinIssues ethics and legal aspectsMatrix Metalloproteinase 9biology.proteinImmunohistochemistryAntibodyDystrophinbusiness
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The disruption of myofibre structures in skeletal muscle after forced lengthening contractions

1998

Specific antibodies against structural proteins (actin, desmin, dystrophin, fibronectin) of muscle fibres were used to study the effect of forced lengthening contractions on muscle microarchitecture. Tibialis anterior (TA) muscle of male Wistar rats were subjected to 240 forced lengthening contractions. At consecutive time points (0, and 6 h, 2, 4, and 7 days) after stimulation, the TA muscle was excised for biochemical and histological assays. β-Glucuronidase activity, a quantitative indicator of muscle damage, showed increased values 2–7 days after the lengthening, peaking on day 4 (11.7-fold increase). A typical course of histopathological changes (myofibre swelling, necrosis and regener…

Pathologymedicine.medical_specialtyNecrosisSkeletal muscleAnatomyBiologyPathology and Forensic Medicinemedicine.anatomical_structurePhysiology (medical)medicinebiology.proteinDesminmedicine.symptomMyofibrilIntermediate filamentDystrophinCytoskeletonActinPathophysiology
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Abnormal accumulation of autophagic vesicles correlates with axonal and synaptic pathology in young Alzheimer's mice hippocampus

2012

Dystrophic neurites associated with amyloid plaques precede neuronal death and manifest early in Alzheimer's disease (AD). In this work we have characterized the plaque-associated neuritic pathology in the hippocampus of young (4- to 6-month-old) PS1(M146L)/APP(751SL) mice model, as the initial degenerative process underlying functional disturbance prior to neuronal loss. Neuritic plaques accounted for almost all fibrillar deposits and an axonal origin of the dystrophies was demonstrated. The early induction of autophagy pathology was evidenced by increased protein levels of the autophagosome marker LC3 that was localized in the axonal dystrophies, and by electron microscopic identification…

Pathologymedicine.medical_specialtyNeuriteClinical NeurologyHippocampusMice TransgenicPlaque AmyloidAmyloid plaquesBiologyHippocampal formationHippocampusDystrophic neuritesPathology and Forensic MedicineAmyloid beta-Protein PrecursorMiceCellular and Molecular NeuroscienceAlzheimer DiseaseAutophagyNeuritesmedicineElectron microscopyLC3AnimalsSenile plaquesMicroscopy ImmunoelectronNeuronsSynaptosomeOriginal PaperPS1/APP transgenic miceCytoplasmic VesiclesAutophagymedicine.diseaseAxonsDisease Models AnimalPresynaptic terminalsAxoplasmic transportNeurology (clinical)Alzheimer's disease
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Pulmonary haemangiolymphangioma – a new entity of pulmonary vascular tumours?

2008

Pathologymedicine.medical_specialtyPediatricsLung NeoplasmsHistologyMEDLINEAntigens CD34Lung pathologyPathology and Forensic MedicineHemangiomaAntibodies Monoclonal Murine-DerivedText miningAntigenBiomarkers TumormedicineHumansHemangioma CapillaryLungLymphangiomabiologybusiness.industryAntibodies MonoclonalGeneral Medicinemedicine.diseaseHemangioma CavernousFluorescent Antibody Technique DirectMonoclonalbiology.proteinAntibodybusinessHistopathology
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Haemangioendothelioma: a current perspective

1995

Pathologymedicine.medical_specialtyPerspective (graphical)medicineSociologyCurrent (fluid)Pathology and Forensic MedicineEpistemologyCurrent Diagnostic Pathology
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Clear Cell Syringoid Carcinoma

2000

Syringoid carcinoma (syringoid "eccrine" carcinoma or eccrine epithelioma) is a rare cutaneous tumor with some controversy regarding its correct definition. It may also be difficult to differentiate from its benign counterpart (syringoma), other adnexal carcinomas, and cutaneous metastasis from adenocarcinomas. We present a case of a syringoid carcinoma of the clear cell variant complemented with an immunohistochemical and ultrastructural study, the latter revealing cytoplasmic accumulation of glycogen and presence of intercellular and intracellular lumina in clear tumor cells, as well as diverse hallmarks of malignancy (i.e., perineural invasion, tumor necrosis, and deep invasion). Clear t…

Pathologymedicine.medical_specialtyPopulationPerineural invasionDermatologyBiologyMalignancyPathology and Forensic MedicineCarcinoembryonic antigenCarcinomamedicineHumanseducationAgedAged 80 and overeducation.field_of_studyScalpCarcinomaS100 ProteinsGeneral Medicinemedicine.diseaseCarcinoembryonic AntigenSweat Gland NeoplasmsClear cell carcinomabiology.proteinKeratinsImmunohistochemistryFemaleClear cellThe American Journal of Dermatopathology
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