Results 51 to 60 of about 10,953 (220)
ACR Open Rheumatology, Volume 8, Issue 1, January 2026.Objectives To evaluate persistence, outcomes, safety, and remission maintenance after switching from intravenous infliximab (IV‐IFX) to subcutaneous infliximab (SC‐IFX, CT‐P13) in patients with Takayasu arteritis (TA). Methods We conducted a prospective, single‐center, proof‐of‐concept observational study of consecutive adults with TA in sustained ...
Luca Iorio +6 more
wiley +1 more source
Eosinophilic granulomatosis with polyangiitis (EGPA) and PRES: a case-based review of literature in ANCA-associated vasculitides [PDF]
, 2015 Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-sized vessel systemic necrotizing vasculitis and belongs to the family of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.
Barilaro, Giuseppe +3 more
core +1 more source
Vessel Wall Inflammation of Takayasu Arteritis Detected by Contrast-Enhanced Magnetic Resonance Imaging: Association with Disease Distribution and Activity. [PDF]
PLoS ONE, 2015 AIMS:The assessment of the distribution and activity of vessel wall inflammation is clinically important in patients with Takayasu arteritis. Magnetic resonance imaging (MRI) is a useful tool, but the clinical utility of late gadolinium enhancement (LGE)
Yoko Kato +6 more
doaj +1 more source
Revista Portuguesa de Cardiologia (English Edition), 2015 Takayasu arteritis is a large vessel vasculitis with various clinical presentations depending on the territories affected. We report the case of a 47-year-old woman who was diagnosed with Takayasu arteritis following rapid progression of coronary disease.
Bernardo, Duque Neves +5 more
openaire +2 more sources
Asian Journal of Endoscopic Surgery, Volume 19, Issue 1, January/December 2026.ABSTRACT Background With the increasing use of minimally invasive surgery, understanding of the precise anatomy involved in median arcuate ligament syndrome (MALS) has advanced. However, surgical strategies and treatment principles for MALS remain unclear.
Hidenori Haruta +14 more
wiley +1 more source
Arterite de takayasu: uma série de casos [PDF]
, 2008 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Nunes, Guilherme Henrique Lopes
core
Noninfectious Necrotizing Aortitis With Predominantly Neutrophilic Infiltrate
Case Reports in Pathology, Volume 2026, Issue 1, 2026.Aortitis can be either infectious or noninfectious, and cases of noninfectious aortitis are not well understood. Our study presents a case of noninfectious ascending aortitis in a relatively young, previously healthy man, characterized by a predominantly neutrophilic infiltrate on histopathological examination without an inciting microorganism.
Nathan A. Williams +4 more
wiley +1 more source
A Rare Case of Giant Cell Arteritis Affecting Two Giants: Pulmonary and Root of Aorta Aneurysm
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Aneurysms of pulmonary arteries and aorta are rare, typically caused by infections, congenital heart defects, vascular abnormalities, or medical interventions. This report presents an unusual case of a 72‐year‐old man with a history of smoking, hypertension, and emphysema, who was found to have a large pulmonary artery aneurysm (63.5 mm) and ...
Gajendra Acharya +5 more
wiley +1 more source
Therapeutic advances in the treatment of vasculitis [PDF]
, 2016 Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core +2 more sources
ESC Heart Failure, 2020 Atypical aortic coarctation is a rare condition associated with Takayasu arteritis, and is characterized by symptoms caused either by hypotension in the lower half of the body or secondary hypertension in the upper half of the body, and heart failure. We
Daigo Hiraya +4 more
doaj +1 more source