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Current Treatment Options in Cardiovascular Medicine, 2008
Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Curry L, Koening, Carol A, Langford
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Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Curry L, Koening, Carol A, Langford
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Current Treatment Options in Cardiovascular Medicine, 1999
Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
, Mohan, , Kerr
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Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
, Mohan, , Kerr
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Management of Takayasu arteritis
Best Practice & Research Clinical Rheumatology, 2023This review overviews the challenges in the assessment of disease activity, damage, and therapy of Takayasu arteritis (TAK). Recently developed disease activity scores for TAK are more useful for follow-up visits and require validation of cut-offs for active disease. A validated damage score for TAK is lacking.
Durga Prasanna Misra +6 more
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Current Rheumatology Reports, 2002
The frequency of Takayasu's arteritis (TA) has been estimated to be 2.9 cases per 1 million people, with a female preponderance, although female-to-male ratio varies from different geographic areas. A high frequency of haplotype A24-B52-DR2 has been found in Japanese patients, without this association in other populations.
Antonio, Fraga, Francisco, Medina
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The frequency of Takayasu's arteritis (TA) has been estimated to be 2.9 cases per 1 million people, with a female preponderance, although female-to-male ratio varies from different geographic areas. A high frequency of haplotype A24-B52-DR2 has been found in Japanese patients, without this association in other populations.
Antonio, Fraga, Francisco, Medina
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Annals of Internal Medicine, 1994
To evaluate prospectively the clinical features, angiographic findings, and response to treatment of patients with Takayasu arteritis.60 patients with Takayasu arteritis were studied at the National Institute of Allergy and Infectious Diseases between 1970 and 1990 and were followed for 6 months to 20 years (median follow-up, 5.3 years).Data on ...
G S, Kerr +6 more
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To evaluate prospectively the clinical features, angiographic findings, and response to treatment of patients with Takayasu arteritis.60 patients with Takayasu arteritis were studied at the National Institute of Allergy and Infectious Diseases between 1970 and 1990 and were followed for 6 months to 20 years (median follow-up, 5.3 years).Data on ...
G S, Kerr +6 more
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Rheumatic Disease Clinics of North America, 1990
The cause of Takayasu's arteritis is still obscure. However, certain aspects of the disease have been greatly clarified over the past decade. The disease is worldwide in distribution, with no ethnic group being totally free from risk of the condition. The inflammatory and stenotic phases of the disease frequently coexist, and it is important that the ...
S, Hall, R, Buchbinder
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The cause of Takayasu's arteritis is still obscure. However, certain aspects of the disease have been greatly clarified over the past decade. The disease is worldwide in distribution, with no ethnic group being totally free from risk of the condition. The inflammatory and stenotic phases of the disease frequently coexist, and it is important that the ...
S, Hall, R, Buchbinder
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Takayasu's Arteritis and Temporal Arteritis
Annals of Vascular Surgery, 1992The giant cell arteritides, temporal arteritis and Takayasu’s arteritis, are granulomatous vasculitides affecting medium and large-sized arteries. Temporal arteritis is a systemic panarteritis affecting the elderly, with greater than 95% of patients being over 50 years of age, although a few case reports in young adults and adolescents exist.
C D, Procter, L H, Hollier
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Takayasu arteritis — five doctors in the history of Takayasu arteritis
International Journal of Cardiology, 1996Takayasu arteritis is a chronic vasculitis mainly involving the aorta, its main branches, pulmonary and coronary arteries. Recent international survey has made clear different sex ratio, different involvement and different clinical manifestations among countries.
F, Numano, T, Kakuta
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Takayasu arteritis in Colombia
International Journal of Cardiology, 1998Takayasu arteritis has been recognized in Colombia just recently, and so far we do not have any report concerning its presentation here. In this first report, some issues related to the presentation of the disease are indicated and compared with those found in the medical literature. No differences were found in age and sex.
C A, Cañas +11 more
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Takayasu arteritis in paediatrics
Cardiology in the Young, 2017AbstractTakayasu arteritis is an idiopathic chronic granulomatous panarteritis predominantly affecting the aorta and its main branches. Although idiopathic, genetic contribution to disease susceptibility is being increasingly recognised. Rare in children, Takayasu arteritis is a worldwide disease with significant morbidity and mortality.
Marisa, Di Santo +2 more
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