Results 61 to 70 of about 10,953 (220)
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Takayasu arteritis is a large vessel vasculitis involving the aorta and its branches. It has a wide spectrum of clinical manifestations and lacks specific diagnostic markers. Here we present a case of a 30‐year‐old female with isolated aortic regurgitation who presented with constitutional symptoms.
Tshering Penjor +5 more
wiley +1 more source
A Rare Cause of Abdominal Pain and Fever of Unknown Origin: Takayasu Arteritis
Journal of Behçet Uz Children's Hospital, 2019 Fever of unknown origin has three most common etiologic categories in children; infectious diseases, connective tissue diseases, and neoplasms. Takayasu arteritis is a chronic vasculitis involving the large vessels, which generally presents with clinical
Özlem Üzüm +5 more
doaj +1 more source
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Takayasu arteritis (TAK) is a rare large‐vessel vasculitis affecting the aorta and its major branches. Although autoimmune mechanisms are central, prior mycobacterial infections have been hypothesized to contribute to the disease onset. A 55‐year‐old South Asian woman with a history of vitiligo and treated multibacillary leprosy presented with
Ujjawal Bhattarai +7 more
wiley +1 more source
The value of [18F]FDG-PET in the diagnosis of large-vessel vasculitis and the assessment of activity and extent of disease [PDF]
, 2018 Purpose: This study was performed to investigate the value of 18F-fluorodeoxyglucose positron emission tomography ([18F]FDG-PET) in the diagnosis of large-vessel vasculitis and the assessment of activity and extent of disease.
Melzer, Ralph +5 more
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Internal Medicine Journal, Volume 55, Issue 12, Page 1985-1996, December 2025.ABSTRACT Background Systemic autoimmune rheumatic diseases (SARDs), including vasculitis, systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM), spondyloarthritis (SpA), Sjogrens disease (SjD) and mixed connective tissue disease (MCTD), are rare but associated with substantial ...
L. Roper +6 more
wiley +1 more source
Imaging infection and inflammation [PDF]
, 2015 No abstract ...
A. W., Glaudemans +3 more
core +1 more source
Antiphospholipid antibody-positive Takayasu arteritis： a case report and literature review
Linchuang shenzangbing zazhiObjectiveTo investigate the clinical features of antiphospholipid antibody-positive Takayasu arteritis and to enhance the awareness of its diagnosis and treatment.MethodsThe clinical features and imaging data of one patient with antiphospholipid antibody-
Wang Ding-ding +7 more
doaj +3 more sources
The Journal of Clinical Hypertension, Volume 27, Issue 12, December 2025.ABSTRACT In this study, we investigated the applicability of the ankle–brachial index (ABI) and brachial–ankle index (BAI) in distinguishing aortic stenosis (AS) from lower‐extremity arterial stenosis. The difference between the ABI on both sides (∆ABI) was defined as the absolute value of the left ABI minus the right ABI. Lower BAI (L‐BAI) was defined
Qian Wang +4 more
wiley +1 more source
True aneurysm of the peripheral pulmonary artery due to necrotizing giant cell arteritis [PDF]
, 2017 Pulmonary artery aneurysm in adults is a rare diagnosis. Most cases described in the literature are either associated with congenital heart disease or pulmonal arterial hypertension, respectively, or are not true aneurysms but rather pseudoaneurysms ...
Gebhart, Florin T.F. +3 more
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Complicação urológica após enxerto aorto-ilíaco: relato de caso e revisão de literatura [PDF]
, 2010 CONTEXT: Ureteral stenosis and ureterohydronephrosis may be serious complications of aortoiliac or aortofemoral reconstructive surgery. CASE REPORT: A 62-year-old female patient presented with a six-month history of left lumbar pain.
BORGES, Leonardo Lima +4 more
core +1 more source