Search results for "astrocytoma"

showing 10 items of 50 documents

Novel clinical insights into spinal hemangioblastoma in adults: a systematic review

2021

ABSTRACT Background Hemangioblastomas are well vascularized, benign CNS tumors and the third most common primary spinal cord tumor after astrocytoma/ependymoma, occurring sporadically or as a part of an autosomal dominant von Hippel-Lindau disease in which tumors are often multiple and prone to relapse. Spinal hemangioblastomas are commonly located in the cervical cord and associated with a syrinx formation. Due to location and growth trends, they may cause significant neurological deficit, impairing patient quality of life. We conducted a systematic review to understand better clinical insights of spinal hemangioblastoma in adults and compare spinal hemangioblastoma versus posterior crania…

EpendymomaAdultmedicine.medical_specialtyvon Hippel-Lindau DiseaseHemangioblastomaMedicineHumansSpinal Cord Neoplasmsadults ; clinical insight ; hemangioblastoma ; outcomes ; spinal cord ; systematic review ; tumorbusiness.industryAstrocytomamedicine.diseaseSpinal cordSyringomyeliaSpinal hemangioblastomaHemangioblastomaSpinal cord tumormedicine.anatomical_structurePosterior cranial fossaQuality of LifeSurgeryNeurology (clinical)RadiologyNeoplasm Recurrence LocalbusinessSyringomyelia
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A Paravermal Trans-Cerebellar Approach to the Posterior Fossa Tumor Causes Hypertrophic Olivary Degeneration by Dentate Nucleus Injury

2021

Background: In brain tumor surgery, injury to cerebellar connectivity pathways can induce a neurodegenerative disease called hypertrophic olivary degeneration (HOD), along with a disabling clinical syndrome. In children, cerebellar mutism syndrome (CMS) is another consequence of damage to cerebello&ndash

EpendymomaCancer Researchmedicine.medical_specialtyCerebellumcerebellumPosterior fossamedulloblastomalcsh:RC254-282ArticleHOD03 medical and health sciences0302 clinical medicineMedicineneurosurgeryMedulloblastomaPilocytic astrocytomabusiness.industryCMSOlivary degenerationmedicine.diseaselcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogensmedicine.anatomical_structureDentate nucleusOncology030220 oncology & carcinogenesisRadiologyNeurosurgerybusiness030217 neurology & neurosurgerycerebellar mutismCancers
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Intracranial pathology of the visual pathway.

2004

Intracranial pathologies involving the visual pathway are manifold. Aligning to anatomy, the most frequent and/or most important extrinsic and intrinsic intracranial lesions are presented. Clinical symptoms and imaging characteristics of lesions of the sellar region are demonstrated in different imaging modalities. The extrinsic lesions mainly consist of pituitary adenomas, meningeomas, craniopharyngeomas and chordomas. In (asymptomatic and symptomatic) aneurysms, different neurological symptoms depend on the location of aneurysms of the circle of Willis. Intrinsic tumors as astrocytoma of any grade, ependymoma and primary CNS-lymphoma require the main pathology in the course of the visual …

EpendymomaPathologymedicine.medical_specialtyAstrocytomaAneurysmPituitary adenomamedicine.arterymedicineHumansRadiology Nuclear Medicine and imagingVisual Pathwaysmedicine.diagnostic_testbusiness.industryBrain NeoplasmsAstrocytomaMagnetic resonance imagingAnatomical pathologyIntracranial AneurysmGeneral MedicineGliomamedicine.diseaseMagnetic Resonance ImagingOptic ChiasmCavernous sinusbusinessCircle of WillisEuropean journal of radiology
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Up-to-date monitoring of childhood cancer long-term survival in Europe: central nervous system tumours.

2007

ABSTRACT Background Tumours of the central nervous system (CNS) account for 15–20% of all malignant childhood tumours in developed countries. Steady improvement of survival of children with CNS tumours has been reported for the past decades. However, these results, obtained by cohort analysis of survival, do not reflect the full extent of recent improvement. Methods Using selected registries from the database of the Automated Childhood Cancer Information System (ACCIS), we calculated period survival estimates for the years 1995–99 for children diagnosed with a malignant CNS tumour. Results The overall 10-year period survival estimate for the years 1995–99 was 59% for children with all CNS t…

EpendymomaPediatricsmedicine.medical_specialtyAdolescentCentral nervous systemAstrocytomaCentral Nervous System NeoplasmsmedicineHumansNeuroectodermal Tumors PrimitiveChildbusiness.industryAge FactorsInfant NewbornAstrocytomaCancerInfantHematologymedicine.diseasePrognosisEuropemedicine.anatomical_structureOncologyEl NiñoEpendymomaChild PreschoolCohortbusinessDeveloped countryCohort studyAnnals of oncology : official journal of the European Society for Medical Oncology
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Pulmonary infiltrate with characteristic “reversed halo” and “air crescent” signs

2016

Male0301 basic medicinePathologymedicine.medical_specialtyAntifungal AgentsPancytopenia030106 microbiologyAstrocytoma030218 nuclear medicine & medical imagingImmunocompromised Host03 medical and health sciences0302 clinical medicineBronchoscopyInternal MedicineHumansMedicineInvasive Pulmonary Aspergillosisbusiness.industryMiddle AgedCombined Modality TherapyAspergillusPulmonary infiltratesVoriconazoleHaloTomography X-Ray Computedbusiness
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Childhood central nervous system tumours – incidence and survival in Europe (1978–1997): Report from Automated Childhood Cancer Information System pr…

2006

Abstract This paper describes the incidence and survival of childhood central nervous system (CNS) tumours in Europe for the period 1978–1997. A total of 19,531 cases, aged 0–14 years, from the ACCIS database were analysed by five regions: the British Isles, East, North, South, and West. Overall age-standardised incidence rate (ASR) of CNS tumours in Europe (1988–1997) was 29.9 per million, with the highest rates in the North. Astrocytoma (ASR = 11.8), primitive neuroectodermal tumours (PNET) (ASR = 6.5) and ependymoma (ASR = 3.4) were the most frequent types. Incidence increased significantly during 1978–1997, on average by 1.7% per year. Diagnostic methods may partially explain incidence …

MaleEpendymomaCancer Researchmedicine.medical_specialtyAdolescentDatabases FactualChildhood cancerCentral nervous systemCentral Nervous System NeoplasmsEpidemiologymedicineHumansRegistriesChildcentral nervous system tumoursbusiness.industryIncidenceIncidence (epidemiology)Infant NewbornInfantChildhood cancers - survival - time trends; central nervous system tumoursAstrocytomaCancermedicine.diseaseSurvival AnalysisSurgeryEuropemedicine.anatomical_structureOncologyEl NiñoChild PreschoolFemalebusinessChildhood cancers - survival - time trendsDemographyEuropean Journal of Cancer
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An international case-control study of maternal diet during pregnancy and childhood brain tumor risk: a histology-specific analysis by food group.

2009

Maternal dietary data from an international collaborative case-control study on childhood brain tumors were used to evaluate associations between histology-specific risk and consumption of specific food groups during pregnancy.Nine study centers from seven countries contributed 1218 cases and 2223 controls. Most cases were diagnosed between 1982 and 1992 and ranged in age from 0 to 19 years. Dietary consumption was measured as average grams per day.Foods generally associated with increased risk were cured meats, eggs/dairy, and oil products; foods generally associated with decreased risk were yellow-orange vegetables, fresh fish, and grains. The cured meat association was specific to astroc…

MaleMESH: Meat ProductsEpidemiologyFood group0302 clinical medicineMESH: Nitroso CompoundsMESH: PregnancyPregnancyRisk FactorsMESH: Risk FactorsMESH: ChildVegetables030212 general & internal medicineChild2. Zero hungerBrain NeoplasmsCruciferous vegetablesMESH: Infant NewbornAstrocytomaMESH: Case-Control StudiesMESH: Infant3. Good healthMeat ProductsQuartileMESH: Young AdultChild PreschoolPrenatal Exposure Delayed Effects030220 oncology & carcinogenesisMESH: Brain NeoplasmsFemaleNitroso Compoundsmedicine.medical_specialtyAdolescent[SDV.CAN]Life Sciences [q-bio]/CancerArticleMESH: Prenatal Exposure Delayed EffectsYoung Adult03 medical and health sciences[SDV.CAN] Life Sciences [q-bio]/CancerMESH: DietInternal medicinemedicineHumansMESH: AdolescentPregnancyMESH: Humansbusiness.industryMESH: Child PreschoolInfant NewbornCase-control studyInfantOdds ratiomedicine.diseaseMESH: VegetablesMESH: MaleDietSurgery[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologieCase-Control StudiesAttributable risk[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologiebusinessMESH: Female
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BLBP-expression in astrocytes during experimental demyelination and in human multiple sclerosis lesions

2011

Several lines of evidence indicate that remyelination represents one of the most effective mechanisms to achieve axonal protection. For reasons that are not yet understood, this process is often incomplete or fails in multiple sclerosis (MS). Activated astrocytes appear to be able to boost or inhibit endogenous repair processes. A better understanding of remyelination in MS and possible reasons for its failure is needed. Using the well-established toxic demyelination cuprizone model, we created lesions with either robust or impaired endogenous remyelination capacity. Lesions were analyzed for mRNA expression levels by Affymetrix GeneChip® arrays. One finding was the predominance of immune a…

MalePathologyPlatelet-derived growth factormedicine.medical_treatmentCell CountBehavioral Neurosciencechemistry.chemical_compoundMice0302 clinical medicineFluorescent Antibody Technique IndirectOligonucleotide Array Sequence AnalysisPlatelet-Derived Growth Factor0303 health sciencesGlial fibrillary acidic proteinbiologyExperimental autoimmune encephalomyelitisAstrocytomaMiddle AgedImmunohistochemistrymedicine.anatomical_structureFemaleFibroblast Growth Factor 2Fatty Acid-Binding Protein 7Adultmedicine.medical_specialtyEncephalomyelitis Autoimmune ExperimentalMultiple SclerosisImmunologyBlotting WesternNerve Tissue ProteinsFatty Acid-Binding ProteinsReal-Time Polymerase Chain ReactionTransfection03 medical and health sciencesCuprizoneCell Line TumorGlial Fibrillary Acidic ProteinmedicineAnimalsHumansRNA MessengerRemyelination030304 developmental biologyAgedEndocrine and Autonomic SystemsMultiple sclerosisGrowth factorTumor Suppressor Proteinsmedicine.diseaseOligodendrocyteMice Inbred C57BLchemistryAstrocytesbiology.proteinOsteopontinCarrier Proteins030217 neurology & neurosurgeryDemyelinating Diseases
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Pediatric High-Grade Astrocytomas Show Chromosomal Imbalances Distinct from Adult Cases

2001

We studied 23 pediatric high-grade astrocytomas by comparative genomic hybridization. Chromosomal imbalances were found in 10 of 10 anaplastic astrocytomas and 11 of 13 glioblastomas and consisted of +1q (43%), +3q (26%), +1p, +2q, +5q (22%), −22q (34%), −6q, −10q (30%), −9q, −11q, −13q, −16q, and −17p (22%). Anaplastic astrocytomas frequently showed +5q (40%), +1q (30%), −22q (50%), −6q, −9q (40%), and −12q (30%); glioblastomas +1q (54%), +3q (38%), +2q, +17q (23%), −6q, −8q, −10q, −13q, and −17p (31%). Minimal common regions mapped to +1q21-41, +3q27-qter, +2q31-32, +5q14-22, −22q12-qter, −10q23-25, −6q25-qter, −9q34.2, −11q14−22, −16q22-qter, and −17p. High-level gains were located on 1q…

MalePathologymedicine.medical_specialtyAdolescentGene DosageAstrocytomaBiologyGastroenterologyPathology and Forensic MedicineInternal medicinemedicineHumansChildChromosome AberrationsBrain NeoplasmsInfantNucleic Acid HybridizationAstrocytomamedicine.diseaseSurvival AnalysisKi-67 AntigenChild PreschoolFemaleGlioblastomaCell DivisionRegular ArticlesGlioblastomaAnaplastic astrocytomaThe American Journal of Pathology
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Gliofibromas (including malignant forms), and gliosarcomas: a comparative study and review of the literature

1993

The presence of connective tissue elements in gliomas necessitates in every case a thorough analysis of the character and derivation of such elements to allow the formulation of an appropriate diagnosis. Four cases are presented in this paper. In cases 1 and 2 (anaplastic astrocytomas in two children, 9 and 4 years old, respectively) all the neoplastic elements were astrocytes and their ability to produce or indirectly promote the production of reticulin and collagen fibers accounted for the presence of such elements in close association with the tumor cells. The term "gliofibroma" has been coined for such tumors, but "desmoplastic astrocytoma", (low grade or anaplastic) or in highly malign…

MalePathologymedicine.medical_specialtyGliosarcomaBrain tumorAstrocytomaHistogenesisPathology and Forensic MedicineCellular and Molecular NeuroscienceGliomamedicineHumansChildAgedBrain Neoplasmsbusiness.industryAstrocytomaSarcomaGliomaMiddle Agedmedicine.diseaseGliofibromaChild PreschoolFemaleNeurology (clinical)SarcomaTomography X-Ray ComputedbusinessAnaplastic astrocytomaActa Neuropathologica
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