Results 51 to 60 of about 5,162 (172)
Antiphospholipid antibody-positive Takayasu arteritis: a case report and literature review
ObjectiveTo 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
A Rare Case of Giant Cell Arteritis Affecting Two Giants: Pulmonary and Root of Aorta Aneurysm
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
New-Onset Ulcerative Colitis in a Young Caucasian Woman with Unclassified Arteritis
Takayasu arteritis is a rare disease mostly found in Asian populations. Cases have been reported in patients with inflammatory bowel disease, suggesting possible genetic linkage.
Bryan Roberts
doaj +1 more source
Superior mesenteric artery pseudoaneurysm in Takayasu arteritis: A case report
Takayasu arteritis is a large vessel arteritis described in young females. It presents with stenotic lesions of the aorta and its branches, although aneurysmal presentation is rare. A 62-year-old woman with Takayasu arteritis was admitted with complaints
Amitabh Satsangi, Sai Divya Yadavalli
doaj
Arterite de Takayasu: a propósito de um caso clínico
Resumo: A arterite de Takayasu é uma vasculite de grandes vasos que cursa com apresentações clínicas diversas consoante os territórios afetados. Apresenta‐se o caso clínico de uma mulher de 47 anos a quem foi feito o diagnóstico de arterite de Takayasu ...
Bernardo Duque Neves +5 more
doaj +1 more source
Late Takayasu Arteritis Diagnosis in a Female Patient With Prior Coronary Artery Bypass Grafting
Takayasu arteritis is a rare cause of cardiovascular morbidity in the Western world. As consequence, vasculitis may be misdiagnosed and treated as atherosclerotic cardiovascular disease. We present a case of late Takayasu arteritis diagnosis, in a female
Ioannis Lianos, MD +5 more
doaj +1 more source
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
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
First case of childhood Takayasu arteritis with renal artery aneurysms
Takayasu arteritis is a large vessel systemic granulomatous vasculitis characterized by stenosis or obliteration of large and medium sized arteries. It commonly involves elastic arteries such as the aorta and its main branches.
Rajhi Hatem +5 more
doaj +1 more source
Central illustration summarizing the comprehensive case management of Takayasu arteritis in a 40‐year‐old female. The figure integrates key aspects: vascular pathology (left subclavian occlusion, right subclavian narrowing, 4.0 cm infrarenal aneurysm), clinical presentation (right arm pain, neck stiffness), inflammatory markers (CRP 18.4 mg/L, ESR 45 ...
Sakib Abrar +5 more
wiley +1 more source

