Results 61 to 70 of about 17,989 (193)

Sweet syndrome: a rare feature of ANCA-associated vasculitis or unusual consequence of azathioprine-induced treatment

open access: yesAllergy, Asthma & Clinical Immunology, 2018
Background Sweet syndrome is a rare skin condition characterised by fever, neutrophilia, and tender erythematous skin lesions and has been reported to occur in association with anti-neutrophil cytoplasmic antibodies (ANCA) as well as complicate treatment
A. U. Arun Kumar   +8 more
doaj   +1 more source

Exercise‐Induced Vasculitis in a 12‐Year‐Old Child: A Case Report

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Exercise‐induced vasculitis (EIV), colloquially known as “Disney rash,” is a benign, self‐limited leukocytoclastic vasculitis of the lower extremities triggered by prolonged exertion in warm weather, well‐recognized in adults but underappreciated in children.
Beverly X. Yu   +3 more
wiley   +1 more source

The effect of plasma exchange in the treatment of anti-neutrophil cytoplasmic antibody-associated small-vessel vasculitis

open access: yesLinchuang shenzangbing zazhi, 2022
Anti-neutrophil cytoplasmic antibody (ANCA) associated small-vessel vasculitis has a high mortality rate. Particularly, patients with renal injury diagnosed by ANCA associated small-vessel vasculitis(AAV) are at high risk of progresses to end-stage renal
Wang Yue-lan   +5 more
doaj  

Granulomatous Vasculitis: An Unusual Manifestation of Metastatic Crohn’s Disease

open access: yes
Australasian Journal of Dermatology, EarlyView.
Ethan Wei Min Lee   +3 more
wiley   +1 more source

Antibiotic‐mediated immune modulation in periodontitis

open access: yesPeriodontology 2000, EarlyView.
Abstract Periodontitis is a chronic inflammatory disease affecting the supporting structures of the teeth. Although initiated by dysbiotic microbial communities, its progression is largely driven by the host's uncontrolled inflammatory response. While antibiotics have conventionally been employed in periodontitis therapy for their antimicrobial ...
Lina J. Suárez   +6 more
wiley   +1 more source

A case of propylthiouracil-induced antineutrophilic cytoplasmic antibody-positive vasculitis successfully treated with radioactive iodine

open access: yesReumatismo, 2013
Antineutrophilic cytoplasmic antibody (ANCA) associated vasculitis is one of the rare complications of propylthiouracil treatment. Having a variable clinical spectrum, it may be presented with both skin limited vasculitis and life-threatening systemic ...
C. Bes   +4 more
doaj   +1 more source

Biosimilar Rituximab in ANCA‐Associated Vasculitis Compared to the Originator: A Multicenter Cohort Study

open access: yesACR Open Rheumatology, Volume 8, Issue 8, August 2026.
Objective To evaluate the six‐month effectiveness and safety of rituximab biosimilars compared to the originator in granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA), and outcomes following originator to biosimilar switching. Methods We recruited adults with GPA or MPA treated with the rituximab originator or a biosimilar for ...
Arielle Mendel   +14 more
wiley   +1 more source

Immnunopathology of ANCA-Associated Vasculitis.

open access: yesInternal Medicine, 1999
During the past few years remarkable progress has been achieved in the understanding of the pathogenic mechanisms leading to vascular inflammation and injury in ANCA-associated vasulitides (AAV): Wegener's granulomatosis (WG), microscopic polyangiitis (MPA) and Churg Strauss syndrome (CSS).
ELENA, Csernok   +2 more
openaire   +3 more sources

Case report: de novo ANCA-associated vasculitis after kidney transplantation treated with rituximab and plasma exchange

open access: yesBMC Nephrology, 2018
Background Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis causes end-stage renal failure in up to a third of cases even with treatment.
Michael S. Sagmeister   +6 more
doaj   +1 more source

Prediction of Relapse and Glucocorticoid Dependence in Eosinophilic Granulomatosis With Polyangiitis: Findings From a Large European Cohort

open access: yesArthritis &Rheumatology, Volume 78, Issue 8, Page 1710-1717, August 2026.
Objective Eosinophilic granulomatosis with polyangiitis (EGPA) is a small vessel vasculitis characterized by eosinophilia, asthma, and ear, nose, and throat (ENT) involvement. Although glucocorticoids (GCs) are effective in controlling symptoms, relapses and GC dependence are common. The aim of this study was to develop predictive models for vasculitis
Matthias Papo   +35 more
wiley   +1 more source

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