Results 1 to 10 of about 37,560 (244)

Drug-induced anti-neutrophil cytoplasmic antibody-associated vasculitis

open access: yesChinese Medical Journal, 2019
. Objective:. In recent years, an increasing number of drugs have been proved to be associated with the induction of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).
Cheng-Hua Weng   +2 more
doaj   +3 more sources

Eosinophils in anti-neutrophil cytoplasmic antibody associated vasculitis

open access: yesBMC Rheumatology, 2019
Background Anti-neutrophil cytoplasmic antibodies associated vasculitides (AAV) are characterized by autoimmune small vessel inflammation. Eosinophils are multifunctional cells with both pro-inflammatory and immunoregulatory properties.
Thomas Hellmark   +4 more
doaj   +3 more sources

Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis [PDF]

open access: yesNature Communications
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a prototypic autoimmune disease, with a subset of AAV patients manifesting anti-myeloperoxidase (MPO) IgG.
CM Wortel   +15 more
doaj   +2 more sources

Splenic Infarcts and Pulmonary Renal Syndrome in a Young Patient with Double-Positive Anti-GBM and ANCA-Associated Vasculitis

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2021
Double-positive disease, defined by double-seropositivity for serum anti-glomerular basement membrane (GBM) antibodies and anti-neutrophil cytoplasmic antibodies (ANCA) is a rare cause of pulmonary-renal syndrome.
Fares T Rajah   +4 more
doaj   +1 more source

Anti-neutrophil cytoplasmic antibodies in leprosy [PDF]

open access: yesClinical Rheumatology, 2006
Anti-Neutrophil Cytoplasmic Antibodies (ANCA) are auto-antibodies directed to intracellular components of neutrophils and used to be considered as present almost exclusively in granulomatous vasculitis. Recently, these auto-antibodies have been found in other autoimmune disorders as well as infectious diseases.We studied patients with leprosy confirmed
Fernando Luiz Barros, Edington   +6 more
openaire   +2 more sources

Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis in Kidney Transplantation

open access: yesMedicina, 2021
Due to complex comorbidity, high infectious complication rates, an elevated risk of relapsing for primary renal disease, as well as inferior recipient and allograft survivals, individuals with anti-neutrophil cytoplasmic antibody (ANCA)-associated ...
Valentina Binda   +3 more
doaj   +1 more source

Differentiation of Cocaine-Induced Midline Destructive Lesions from ANCA-Associated Vasculitis [PDF]

open access: yesIranian Journal of Otorhinolaryngology, 2018
Introduction: Cocaine-induced midline destructive lesions (CIMDL) are complications of regular nasal cocaine inhalation. CIMDL can mimic systemic diseases with positive anti-neutrophil cytoplasmic antibodies (ANCA), such as granulomatosis with ...
Alireza Mirzaei   +2 more
doaj   +1 more source

Hydralazine-induced anti-neutrophil cytoplasmic antibody-positive renal vasculitis presenting with a vasculitic syndrome, acute nephritis and a puzzling skin rash: a case report

open access: yesJournal of Medical Case Reports, 2013
Introduction Anti-neutrophil cytoplasmic antibody-associated vasculitis has been associated with many drugs and it is a relatively rare side effect of the antihypertensive drug hydralazine.
Keasberry Justin   +5 more
doaj   +1 more source

When Anti-Neutrophil Cytoplasmic Antibody Fails: A Case of Anti-Neutrophil Cytoplasmic Antibody Negative Granulomatosis With Polyangiitis [PDF]

open access: yesCureus, 2020
Granulomatosis with polyangiitis (GPA) is a vasculitis of small and medium-sized vessels and presents with varying signs and symptoms. It includes upper and lower airway manifestations and glomerulonephritis with a positive antineutrophil cytoplasmic antibody (ANCA) in serology in 90% of cases.
Gangireddy, Mounika   +4 more
openaire   +2 more sources

An atypical presentation of cardiac tamponade and periorbital swelling in a patient with eosinophilic granulomatosis with polyangiitis: a case report

open access: yesJournal of Medical Case Reports, 2017
Background Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. Case presentation We report a case of eosinophilic
Alexandra C. Keefe   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy