Search results for "Vasculitide"

showing 3 items of 3 documents

Respiratory manifestations of eosinophilic granulomatosis with polyangiitis (Churg-Strauss)

2016

The respiratory manifestations of eosinophilic granulomatosis with polyangiitis (EGPA) have not been studied in detail.In this retrospective multicentre study, EGPA was defined by asthma, eosinophilia and at least one new onset extra-bronchopulmonary organ manifestation of disease.The study population included 157 patients (mean±sd age 49.4±14.1 years), with a mean±sd blood eosinophil count of 7.4±6.4×109 L−1 at diagnosis. There was a mean±sd of 11.8±18.2 years from the onset of asthma to the diagnosis of EGPA, of 1.4±8.4 years from the first onset of peripheral eosinophilia to the diagnosis of EGPA, and of 7.4±6.4 years from EGPA diagnosis to the final visit. Despite inhaled and oral corti…

MalePediatricsAdministration OralDiseaseChurg-Strauss SyndromeBronchoalveolar LavageSeverity of Illness Index0302 clinical medicineAdrenal Cortex HormonesEosinophilicEosinophiliaAged 80 and overNomenclatureSystemic VasculitisCohortMiddle AgedTerm-follow-upPrognosis3. Good healthRespiratory Function TestsManagementTreatment OutcomeCohortAntineutrophil cytoplasmic antibodiesPopulation studyFemaleFrancemedicine.symptomGranulomatosis with polyangiitisConsensus conferencePulmonary and Respiratory MedicineAdultmedicine.medical_specialtyAdolescentVasculitides[ SDV.EE.SANT ] Life Sciences [q-bio]/Ecology environment/HealthGranulomatosis03 medical and health sciencesYoung AdultEosinophiliamedicineHumansAnti-neutrophil cytoplasmic antibodyAsthmaAgedRetrospective Studies030203 arthritis & rheumatology[SDV.EE.SANT]Life Sciences [q-bio]/Ecology environment/Healthbusiness.industryGranulomatosis with Polyangiitisasthmamedicine.diseaseEosinophils030228 respiratory systemImmunologybusinessTomography X-Ray Computed
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Cell Immunity in Inflammatory Vasculitis

2015

The vasculitides are a highly heterogeneous group of disorders characterized by the presence of inflammatory leukocytes in the vessel walls and reactive inflammation. Giant cell arteritis (GCA) and Takayasu’s arteritis (TA) are the two primary large-vessel vasculitides. Two distinct cellular pathways have been identified in GCA: Th17 polarization and IL-17 secretion and generation of Th1 cells which secrete IFN-γ. These two pathways may play different roles in the pathogenesis of vasculitides. The antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are small vessel vasculitis associated with antibodies directly to myeloperoxidase (MPO-ANCA) such as eosinophilic granulo…

TakayasuVasculitisSettore MED/16 - ReumatologiaANCAHortonImmunologyVasculitideImmunology and AllergyBehçet syndromeGiant cell vasculiti
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Patogeneza zapaleń naczyń związanych z przeciwciałami przeciwko cytoplazmie neutrofilów

2018

Zapalenia naczyń związane z przeciwciałami przeciwko cytoplazmie neutrofilów (antineutrophil cytoplasmic antibodies-associated vasculitis – AAV) to grupa chorób zajmujących małe naczynia i charakteryzujących się ich martwiczym zapaleniem oraz obecnością przeciwciał przeciwko cytoplazmie neutrofilów (antineutrophil cytoplasmic antibodies – ANCA) przy braku lub obecności jedynie skąpej ilości immunoglobulin w ścianie naczyń. Przeciwciała przeciwko cytoplazmie neutrofilów to przeciwciała klasy G skierowane przeciwko składnikom ziarnistości granulocytów obojętnochłonnych. Dowody na udział ANCA w patogenezie AAV pochodzą zarówno z obserwacji klinicznych, badań in vitro, jak i badań na zwierzętac…

antineutrophil cytoplasmic antibodieszapalenia naczyńvasculitidesprzeciwciała przeciwko cytoplazmie neutrofilówPomeranian Journal of Life Sciences
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