ARTIGO ORIGINAL. Arterite de Takayasu: aspectos clínicos e terapêuticos em 36 pacientes. Takayasu’s arteritis: clinical and therapeutic aspects in 36 patients. Disease definition. Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large . Request PDF on ResearchGate | On Jan 1, , A.Z. Castellanos and others published Arterite de Takayasu.

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The earliest detectable lesion is a local narrowing or irregularity of the lumen. Check this box if you wish to receive a copy of your message.

Artérite de Takayasu — Wikipédia

In the Western worldatherosclerosis is a more frequent cause of obstruction of the aortic arch vessels than Takayasu’s arteritis. J Vasc Surg ; Ann Intern Med takyasu The initial “inflammatory phase” is often followed by a secondary “pulseless phase”. She continued under medical care at a basic healthcare unit in her own district, where she used to present nonspecific symptoms such as fatigue, diffuse arthralgia, dizziness, intermittent claudication, diffuse myalgia, tachycardia, and depressive symptoms.

Although the cause of Takayasu arteritis adterite unknown, the condition is characterized by segmental and patchy granulomatous inflammation of the aorta and its major derivative branches.


Artérite de Takayasu

Renal revascularization in Takayasu arteritis-induced renal artery stenosis. As with all aneurysms, the possibility of rupture and vascular bleeding is existent and requires monitoring.

AdultAdolescent ICD Goodpasture’s syndrome Sneddon’s syndrome.

Andrews J, Mason JC. Renal-artery stenosis in a patient with Takayasu’s arteritis. Acta Societatis ophthalmologicae JaponicaeTokyo Journal of General Internal Medicine.

Acute hemorrhagic arterote of infancy Cryoglobulinemic vasculitis Bullous small vessel vasculitis Cutaneous small-vessel vasculitis. We present in this report the case of an elderly patient with late diagnosis of Takayasu’s arteritis and various comorbidities or related complications. Additional genetic variants and the classical HLA alleles were imputed and analyzed.

Left anterior oblique angiographic image of Takayasu’s arteritis showing areas of stenosis in multiple great vessels. Takayasu’s Arteritis in a Patient with Sydenham’s Chorea: This may develop into stenosis and occlusion. Promising results are achieved with mycophenolate and tocilizumab [13].

A rare complication of this condition are coronary artery aneurysms. Mitral-aortic intervalvular fibrosa involvement by takayasu’ arteritis.

Takayasu’s arteritis

The most commonly affected vessel is the subclavian artery, while renal artery stenosis is relatively uncommon. It mainly affects the aorta the main blood vessel leaving the heart and its branches, as well as taayasu pulmonary arteries. Other search option s Alphabetical list. Chronic total occlusion and successful drug-eluting stent placement in Takayasu arteritis-induced renal artery stenosis.


Those with the disease often notice symptoms between 15 and takyaasu years of age. Takayasu arteritis TAK is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

For patients who do not respond to steroids may require revascularization, either via vascular bypass or angioplasty and stenting. Two Japanese physicians at the same meeting Drs. Imaging findings in Takayasu’s arteritis. Chronic and slow-developing TA -the clinical setting that is the most frequent, causes vascular lesion characterized by thickening of the adventitia and cellular infiltration of the tunica media, with local destruction of smooth muscle cells and elastin of the vessels.

Int Cardiovasc Res J ;8: Specialised Social Services Eurordis directory. Takayasu’s arteritis Giant-cell arteritis.