ARTERITE DE TAKAYASU PDF

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.

Author: Gukree Gardagar
Country: Gabon
Language: English (Spanish)
Genre: Environment
Published (Last): 28 November 2008
Pages: 214
PDF File Size: 20.19 Mb
ePub File Size: 3.21 Mb
ISBN: 377-7-84856-158-7
Downloads: 96199
Price: Free* [*Free Regsitration Required]
Uploader: Molabar

Some people develop an initial “inflammatory phase” taakyasu by systemic illness with signs and symptoms of malaisefevernight sweatsweight lossjoint painfatigueand fainting. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. The age at onset helps to differentiate Artwrite arteritis from other types of large vessel vasculitis. This page was last edited tqkayasu 18 Decemberat In the Western worldatherosclerosis is a more frequent cause of obstruction of the aortic arch vessels than Takayasu’s arteritis.

Rev Port Cardiol ; Females are about 8—9 times more likely to be affected than males. Only comments written in English can be processed. 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.

In other projects Wikimedia Commons. Journal of General Internal Medicine.

Goodpasture’s syndrome Sneddon’s syndrome. If treatment is not kept to a high standard, long-term damage or death can occur. In one of these visits, she complained of recent oliguria, slowness, drowsiness and hair loss. Archived from the original on Health care resources for this disease Expert centres Diagnostic tests 3 Patient organisations 23 Orphan drug s 0.

  CALATORIA LUI VLAD IN CELALALT TARAM PDF

Takayasu’s arteritis-recent advances in imaging offer promise. The earliest detectable lesion is a local narrowing or irregularity of the lumen.

Clinical and statistical analyses of related prognostic factors” PDF. Clin Med Res ; Takayasu’s Arteritis in a Patient with Sydenham’s Chorea: We present in this report the case of an elderly patient with late diagnosis of Takayasu’s arteritis and various comorbidities or related complications.

Of note is the function of renal artery stenosis in the causation of high blood pressure: Ann Intern Med ; In this new hospital stay, the patient showed signs of dehydration and new exacerbation of her chronic kidney disease, with creatinine at 3.

arterite de Takayasu – Wiktionary

Because of the significant side effects of long-term high-dose prednisone use, the starting dose is tapered over several weeks to a dose which controls symptoms while limiting the side effects of steroids. Onishi and Kagoshima reported similar eye findings in individuals whose wrist pulses were absent.

The eye findings described by Takayasu are rarely seen in patients from North America and British Columbia. Takayasu’s arteritis is similar to other forms of vasculitis, including giant cell arteritis which typically affects older individuals.

arterite de Takayasu

Stenosis of the renal arteries causes hypoperfusion decreased blood flow of the juxtaglomerular apparatus arterie, resulting in exaggerated secretion of renin, and high blood levels of aldosteroneeventually leading to water and salt retention and high blood pressure.

Coronal MRA showed an occlusion of the left subclavian artery, of the right common iliac artery and also of the superior mesenteric artery with moderate stenosis in the middle third of the right renal artery.

  74F244 DATASHEET PDF

This work is licensed under a Creative Commons Attribution 4. The clinical presentation is nonspecific, with signs and symptoms that vary according to the affected arterial segment. D ICD – Rev Bras Reumatol ;epub ahead of print. Her physical examination revealed blood pressure BP not measurable in the left arm, murmurs in her left-side subclavian and carotid arteries and femoral pulse difference between the legs.

Takayasu arteritis TA is a rare chronic granulomatous inflammatory arterial disease of unknown etiology that may affect the aorta and its main branches. It is now known that the blood vessel malformations that occur in the retina are an angiogenic response to the arterial narrowings in the neck and that the absence of pulses noted in some people occurs because of narrowings of the blood vessels to the arms.

Fainting may result from subclavian steal syndrome or carotid sinus hypersensitivity. Takayasu’s arteritis Giant-cell arteritis.

Relevant Facts

Contrast angiography has been the gold standard. Since then, the bearer of heart failure, atrial fibrillation, and dyslipidemia, without a diagnosis of hypertension SAH. As with all aneurysms, the possibility of rupture and vascular bleeding is existent and requires monitoring. Takayasu arteritis is a rare disease of unknown etiology that affects the aorta and its main branches. Other search option s Alphabetical list.