Results 71 to 80 of about 41,602 (220)

Atypical Tolosa Hunt syndrome with bilateral sclerokeratitis and optic atrophy in Takayasu's arteritis

open access: yesAmerican Journal of Ophthalmology Case Reports, 2017
Purpose: We report an interesting case of atypical Tolosa Hunt syndrome with bilateral Sclerokeratitis and optic atrophy in a patient with Takayasu's arteritis.
Kalpana Babu, Deepika C. Parameswarappa
doaj   +1 more source

Takayasu's arteritis - a comprehensive review

open access: yes, 2017
Takayasu’s arteritis (TA) is a chronic inflammatory disease of unknown aetiology. The mechanism of this disease is not exactly defined. The inflammatory process is generally (but not exclusively) initiated in the second or third decade of life through ...
Natraj Setty
semanticscholar   +1 more source

Effectiveness of Four‐Limb Blood Pressure in Distinguishing Between Aortic Stenosis and Bilateral Lower‐Extremity Arterial Stenosis

open access: yesThe 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

Beyond the Pulselessness: A Multifaceted Case of Takayasu Arteritis With Aneurysmal Complications and Extensive Upper Limb Vascular Occlusion in a 40‐Year‐Old Female

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
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

Cerebral Embolic Activity in a Patient during Acute Crisis of Takayasu’s Arteritis

open access: yesCase 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

Coronary Fistula Between the Left Anterior Descending Coronary Artery and the Pulmonary Artery: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Timely diagnosis and management of coronary artery fistulas are vital to prevent complications. Advanced imaging and multidisciplinary care aid accurate treatment. Clinicians should consider coronary artery fistula in unexplained cardiac symptoms. When resources are limited, innovation like intraoperative fluoroscopy can ensure success. Always
Mohammad Qaiser Aziz Khan   +4 more
wiley   +1 more source

Janus Kinase inhibitors in the treatment of large vessel vasculitis: a systematic review and meta-analysis

open access: yesOpen Medicine
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

Takayasu arteritis [PDF]

open access: yesEuropean Journal of Cardio-Thoracic Surgery, 2011
Matthew, Kurien   +2 more
openaire   +2 more sources

Acute ischemic cholecystitis in Takayasu’s syndrome – a rare finding [PDF]

open access: yesArchives 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  

Spontaneous Coronary Artery Dissection in a Male Patient with Takayasu’s Arteritis and Antiphospholipid Antibody Syndrome

open access: yesCase 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

Home - About - Disclaimer - Privacy