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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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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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Update on Takayasu's arteritis
La Presse Médicale, 2015Takayasu arteritis (TAK) is a rare, chronic large-vessel vasculitis (LVV) that predominantly affects aorta, its major branches and the pulmonary arteries. Recent advances in the genetics, clinical course, prognosis, disease assessment with biomakers/imaging/new scoring systems and new treatment options in TAK are discussed in this review.
Fatma, Alibaz-Oner, Haner, Direskeneli
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International Journal of Cardiology, 1996
Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years.
Turkoglu, C +7 more
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Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years.
Turkoglu, C +7 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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Pregnancy and Takayasu's arteritis
The American Journal of Medicine, 1983Thirteen patients with Takayasu's arteritis had 30 pregnancies between 1970 and 1982. The 11 pregnancies occurring before the disease became clinically evident were uneventful. Eleven patients had 19 pregnancies after manifestation of the disease. Four ended in abortion, four in cesarean section, and 11 in uneventful vaginal delivery at term. There was
V C, Wong, R Y, Wang, T F, Tse
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Treatment of Takayasu's Arteritis
Annals of Internal Medicine, 1986Excerpt To the editor: The prospective analysis by Shelhamer and colleagues (1) of 20 patients seen at the National Institute of Health is a valuable contribution to the study of Takayasu's arterit...
S, Hall, G G, Hunder
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Rheumatic Disease Clinics of North America, 1994
Takayasu's arteritis has become increasingly recognized as a worldwide entity with a variable spectrum of disease expression. Although evidence for immune mechanisms of disease exist, the precise etiopathogenesis remains elusive. Improvements in the evaluation of disease activity beyond the current parameters of clinical symptoms, erythrocyte ...
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Takayasu's arteritis has become increasingly recognized as a worldwide entity with a variable spectrum of disease expression. Although evidence for immune mechanisms of disease exist, the precise etiopathogenesis remains elusive. Improvements in the evaluation of disease activity beyond the current parameters of clinical symptoms, erythrocyte ...
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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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