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Takayasu's Arteritis: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association, 2022
Takayasu's arteritis is a chronic vasculitis of medium and large vessels. The most involved vessel is the aorta and its major branches. The disease is primarily seen in young women.
Arzoo Khadka   +2 more
doaj   +2 more sources

Adolescent Takayasu's arteritis with hypertensive intracerebral hemorrhage: a case report and literature review [PDF]

open access: yesFrontiers in Pediatrics
Takayasu's arteritis is a primary systemic vasculitis that affects predominantly large vessels, affecting the aorta and its major branches. We report a case of adolescent female patient who initially experienced numbness and weakness in her limbs ...
Fang Zhang   +8 more
doaj   +2 more sources

Takayasu's arteritis causing coronary stenosis with myocardial ischemia, severe aortic regurgitation, and pericarditis [PDF]

open access: yesRadiology Case Reports
Takayasu's Arteritis (TA) is a rare, chronic large-vessel vasculitis that can lead to severe cardiac complications and life-threatening outcomes. Early diagnosis is essential for improving patient prognosis, but its nonspecific clinical presentation and ...
Ana Álvarez Vázquez, MD   +8 more
doaj   +2 more sources

Takayasu's arteritis presenting with temporary loss of vision in a 23-year-old woman with beta thalassemia trait: a case report [PDF]

open access: yesJournal 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   +3 more sources

Takayasu’s Arteritis: A Special Case Report and Review of the Literature [PDF]

open access: yesMedicina
Background: Takayasu’s arteritis is a rare type of vasculitis with severe complications like stroke, ischemic heart disease, pulmonary hypertension, secondary hypertension, and aneurysms.
Paloma Moisii   +4 more
doaj   +2 more sources

Multiple sclerosis in a patient with Takayasu’s Arteritis: A case report [PDF]

open access: yesCaspian Journal of Internal Medicine
Background: Multiple sclerosis (MS) and Takayasu's arteritis (TAK) are two autoimmune diseases that affect the Central nervous system (CNS), but the relationship between them has not been established. Case Presentation: Here we report the emergence of MS
Mohammad Mehdi Emam   +4 more
doaj   +2 more sources

The efficacy of interleukin-6 inhibitor tocilizumab for takayasu’s arteritis, after insufficient response to previous treatment with glucocorticoids, methotrexate, cyclophosphamide, fludarabine. (A case report)

open access: yesНаучно-практическая ревматология, 2021
Thanks to progress in understanding of Takayasu’s arteritis pathogenesis, the role of biological therapies is expanding, especially in refractory diseases.
V. N. Antipova   +2 more
doaj   +1 more source

Takayasu's disease presenting with tubercular empyema: A rare presentation of a rare disease

open access: yesJournal of the Scientific Society, 2023
Takayasu's disease (TD) also known as pulseless disease is an arteriopathy characterized by vasculitis affecting the aorta and its branches. It is also known as aortic arch syndrome, nonspecific aorto-arteritis, and young female arteritis.
Neha Gajanan Phate   +4 more
doaj   +1 more source

Difficulties in the Diagnosis and Management of Patients with Takayasu’s Arteritis: A Description of a 5-Year Clinical Follow-Up

open access: yesАрхивъ внутренней медицины, 2023
Takayasu’s disease (nonspecific aortoarteritis) is a granulomatous inflammation of the aorta and its main branches with a progressive course and development of severe ischemic disorders. The difficulty of diagnosis and the possibility of applying various
A. V. Petrov   +6 more
doaj   +1 more source

Takayasu's arteritis: A rare cause of cardiac death in a Caucasian teenage female patient [PDF]

open access: yes, 1997
A Caucasian teenage Dutch schoolgirl with known chronic low visual acuity and albinism, presented with frank acute pulmonary oedema, died after 1 h of cardio-pulmonary resuscitation for bradyarrhythmia and cardiac arrest. Two weeks prior to presentation,
Hollander, J.C. (Jan) den   +2 more
core   +5 more sources

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