Conventional and ct angiographic diagnosis of takayasu arteritis. Takayasu arteritis tak is a rare inflammatory largevessel vasculitis primarily affecting the aorta and its major branches, but also other large. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Mar 12, 2019 it is named after the japanese professor mikito takayasu who first described the findings of the disease in the young japanese population group. Vessel inflammation leads to wall thickening, fibrosis, stenosis, and thrombus formation. Nov 03, 20 takayasu arteritis is a condition that causes inflammation of the main blood vessel that carries blood from the heart to the rest of the body and its associated branched blood vessels. A seven years olf female was admitted to luis calvo mackenna childrens hospital. It is named after the japanese professor mikito takayasu who first described the findings of the disease in the young japanese population group. For purposes of classification, a patient shall be said to ahve takayasu arteritis if at least 3 of these 6 criteria are present. Takayasu arteritis, also known as pulseless disease, occlusive thromboaortopathy, and martorell syndrome, 1 is a chronic inflammatory arteritis affecting large vessels, predominantly the aorta and its main branches. Giant cell arteritis and takayasu arteritis large vessel. Takayasu arteritis genetic and rare diseases information. Tiene amplia distribucion mundial, con gran prevalencia en asia 6. The clinical experience derived from the retrospective study of 107 cases of ta over a 19 year period is presented.
3 641 317 812 1579 1148 1133 768 145 719 421 468 716 1322 331 1284 389 1598 1515 360 112 230 694 914 299 556 187 31 1403 656