Takayasu Arteriitis

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Takayasu arteritis: a review.

Takayasu arteritis is a well known yet rare form of large vessel vasculitis. This review details the history, clinical features, differential diagnoses, classification, and immunology of the disorder. Suppression of inflammation and preservation of vascular competence are the aims of treatment. As with any rare disease, randomised controlled treatment trials are either lacking or based on small...

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Takayasu arteritis--beyond pulselessness.

Takayasu Arteritis is a chronic vasculitis, mainly involving the aorta and its main branches, as well as the coronary and pulmonary Arteritis to cause stenosis, and/or obstruction due to thrombusformation or aneurysmalformation and/or rupture of the involved arteries (1, 2) (Fig. 1). The first description of this morbid condition was reported in 1830 by Yamamoto in Japan (3). However, the first...

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Takayasu arteritis in pregnancy.

Takayasu arteritis is a chronic, granulomatous arteritis affecting large and medium-sized arteries. During pregnancy, maternal and foetal complications are largely as a consequence of maternal arterial hypertension. We present a case of a 35-year-old para one gravida two patient with Takayasu arteritis (group III disease) complicated by chronic hypertension and a severely dilated ascending aort...

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Takayasu arteritis in children

Takayasu arteritis (TA) is a large vessel vasculitis that usually affects young female patients during the second and third decades of life, but has been reported in children as young as 24 months of age. Aim of this report was to describe four children (two girls) with TA, as well as summarizing main published studies. The mean age at presentation of our cases was 11 years (range 8-15). Three ...

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ژورنال

عنوان ژورنال: European Journal of Vascular and Endovascular Surgery

سال: 2015

ISSN: 1078-5884

DOI: 10.1016/j.ejvs.2014.09.003