Results 41 to 50 of about 5,320 (136)
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed +4 more
wiley +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
Superior mesenteric artery pseudoaneurysm in Takayasu arteritis: A case report
Turkish Journal of Vascular Surgery, 2020 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
New-Onset Ulcerative Colitis in a Young Caucasian Woman with Unclassified Arteritis
Case Reports in Vascular Medicine, 2022 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
Granulomatous Vasculitis: An Unusual Manifestation of Metastatic Crohn’s Disease
Australasian Journal of Dermatology, EarlyView.
Ethan Wei Min Lee +3 more
wiley +1 more source
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.Objective This systematic review documents the current status of extracorporeal membrane oxygenation (ECMO) use in patients with complications of rheumatologic diseases. Methods Following Preferred Reporting Items for Systematic Reviews and Meta Analyses 2020 guidelines, we conducted a systematic review of studies published from January 2019 to ...
Kari L. Falaas +3 more
wiley +1 more source
Arterite de Takayasu: a propósito de um caso clínico
Revista Portuguesa de Cardiologia, 2015 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
JACC: Case Reports, 2020 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
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.Objective Gain‐of‐function variants in IDH1 and IDH2 are enriched among individuals with coexisting myeloid neoplasms and autoimmune diseases. However, the association between IDH1/IDH2 variants and rheumatic diseases independent of hematologic neoplasms remains unclear. We investigated the association between rare gain‐of‐function and loss‐of‐function
Mahmut S. Kaymakci +3 more
wiley +1 more source
First case of childhood Takayasu arteritis with renal artery aneurysms
Pediatric Rheumatology Online Journal, 2010 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