Results 51 to 60 of about 1,863 (134)
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
ABSTRACT Takayasu arteritis (TA) is a rare chronic granulomatous large‐vessel vasculitis predominantly affecting the aorta and its major branches, leading to stenosis, occlusion, or aneurysm formation. It typically presents in young women, though atypical cases can occur in older adults.
Chao Liu +6 more
wiley +1 more source
Granulomatous Vasculitis: An Unusual Manifestation of Metastatic Crohn’s Disease
Australasian Journal of Dermatology, Volume 67, Issue 5, Page e333-e334, August 2026.
Ethan Wei Min Lee +3 more
wiley +1 more source
Cerebral Embolic Activity in a Patient during Acute Crisis of Takayasu’s Arteritis
Takayasu’s arteritis is a disease that affects large vessels and may cause neurological symptoms either by stenoses/occlusions or embolisms from vessels with an inflammatory process.
Ricardo de Carvalho Nogueira +3 more
doaj +1 more source
This meta-analysis evaluates Janus Kinase (JAK) inhibitors’ efficacy and safety in large vessel vasculitis (LVV), encompassing Giant Cell Arteritis (GCA) and Takayasu’s Arteritis (TAK).
Bai Yang, Wang Zhe, Zhang Chunling
doaj +1 more source
Acute ischemic cholecystitis in Takayasu’s syndrome – a rare finding [PDF]
Introduction. Takayasu’s arteritis or pulseless disease is a systemic inflammatory disease of an unknown etiology, affecting medium and large arteries and their branches, leading to stenosis, occlusions, or aneurysmal degeneration. It is more frequent in
Bogdan SOCEA +7 more
doaj
We present a case of a 34-year-old male who presented to the emergency ward with fever and abdominal pain. The diagnosis of Takayasu’s arteritis and also antiphospholipid syndrome was made during an imaging workup of deep-vein thrombosis.
Demet Menekşe Gerede +7 more
doaj +1 more source
Successful Pregnancy in a Patient with Takayasu’s Arteritis: a Case Report
<p><strong>Background and objectives</strong></p><p>Takayasu’s arteritis, so-called pulseless disease, is a syndrome mostly seen in young women. It is a chronic inflammatory arteritis affecting large vessels.
Z Ebrahimi
doaj
Introduction The simultaneous presence of Takayasu's arteritis and beta thalassemia trait is a rare combination. To the best of our knowledge, this is the first case report on Takayasu's arteritis and beta thalassemia presenting together.
Shabbir Fahad A, Ishaq Mohammad G
doaj +1 more source
Re-do aortic operation in a young patient for aggressive Takayasu’s arteritis
Takayasu’s arteritis is an inflammatory arteriopathy which involves the aorta and its major branches, causing mainly stenosis of their lumen, though aneurysmal lesions can also occur.
Bougioukas Ioannis +3 more
doaj +1 more source

