Results 61 to 70 of about 1,687 (159)
Clinical Case Reports, Volume 14, Issue 6, June 2026.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
The story of Takayasu arteritis [PDF]
Rheumatology, 2002 Takayasu arteritis is a chronic vasculitis mainly involving the aorta and its main branches, such as the brachiocephalic, carotid, subclavian, vertebral and renal arteries, as well as the coronary and pulmonary arteries. It induces clinically varied ischaemic symptoms due to stenotic lesions or thrombus formation, including blindness, cataract anduor ...
openaire +2 more sources
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
Case Reports in Neurology, 2012 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
Journal of Medical Case Reports, 2011 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
Open MedicineThis 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
Case Reports in Rheumatology, 2013 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
Acute ischemic cholecystitis in Takayasu’s syndrome – a rare finding [PDF]
Archives of the Balkan Medical Union, 2018 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
Successful Pregnancy in a Patient with Takayasu’s Arteritis: a Case Report
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2012 <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