Results 101 to 110 of about 30,114 (242)

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).
E, Csernok, A, Müller, W L, Gross
openaire   +3 more sources

Orbital pseudotumour masquerading as Wegener’s granulomatosis [PDF]

open access: yes, 2015
A twenty-two year old female patient presented with new onset bilateral hard orbital masses and progressively worse tear lake problems. Computed tomography of the orbits revealed poorly differentiated bilateral orbital masses.
Fenech, Matthew, Fenech, Thomas
core  

Is serum HMGB1 a biomarker in ANCA-associated vasculitis? [PDF]

open access: yes, 2013
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are systemic inflammatory disorders that include granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), Churg-Strauss syndrome and renal limited ...
Bijl, Marc   +6 more
core   +3 more sources

A case of propylthiouracil induced antineutrophil cytoplasmic antibody associated vasculopathy

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Nikhil Dwivedi   +2 more
wiley   +1 more source

Severe Adult HLH/MAS With SPTCL‐Like Panniculitis: A Phenotype‐Guided, Resource‐Adapted Therapeutic Strategy Without Cytotoxic Therapy

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
Graphical abstract illustrating the phenotype‐guided therapeutic approach in severe adult HLH/MAS with SPTCL‐like panniculitis, demonstrating clinical and biochemical response following sequential treatment with therapeutic plasma exchange, intravenous immunoglobulin, and cyclosporine.
Hatem Mousa Taha   +2 more
wiley   +1 more source

Anticuerpos anticitoplasma del neutrófilo en la clasificación de las vasculitis sistémicas

open access: yesRevista Cubana de Medicina, 2003
La detección de los anticuerpos anticitoplasma del neutrófilo (ANCA) constituye el diagnóstico inmunológico de las vasculitis sistémicas. Este trabajo estuvo dirigido a probar la utilidad clínica del método de inmunofluorescencia indirecta (IFI) sobre ...
Elena Kokuina   +3 more
doaj  

Subacute parkinsonism associated with proteinuria, hematuria, and PR3-ANCA positivity: a diagnostic challenge

open access: yesBMC Neurology
Background Secondary causes of parkinsonism, such as tumors and autoimmune conditions, are rare. Cases of parkinsonism owing to antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis of the central nervous system (CNS) or lymphoma are scarce ...
Akisato Nishigaki   +12 more
doaj   +1 more source

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

Coexisting Hepatic and Renal Dysfunction During Pulmonary Tuberculosis Treatment: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Anti‐tuberculosis therapy may rarely cause concurrent liver and kidney injury, with ANCA positivity suggesting immune involvement. This case highlights the importance of early recognition, treatment modification, and multidisciplinary care to prevent complications and ensure effective tuberculosis management.
Irfan Malik   +7 more
wiley   +1 more source

Linked help from bacterial proteins drives autoantibody production in small vessel vasculitis. [PDF]

open access: yes, 2018
The small vessel vasculitides granulomatosis with polyangiitis (GPA) and microscopic polyangiitis are associated with autoantibodies to neutrophil cytoplasm antigens (ANCA), principally proteinase-3 (PR3) and myeloperoxidase (MPO).
Oliveira, DBG
core   +1 more source

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