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 patient continued treatment with corticosteroids for three months only, after which he stopped and did not return to the angiologist. The documents contained in xrterite web site are presented for information purposes only. AdultAdolescent ICD Takayasu’s arteritis Giant-cell arteritis. One rare, important feature of the Takayasu’s arteritis is ocular involvement in form of visual field defects, vision loss, or retinal hemorrhage.

Artérite de Takayasu

Andrews’ Diseases of the Skin: The earliest detectable lesion is a local narrowing or irregularity of the lumen. Takayasu’s arteritis also known as Takayasu’s disease”aortic arch syndrome,” “nonspecific aortoarteritis,” and “pulseless disease” [1]: Nephrol Dial Transplant ; J Vasc Surg ; Andrews J, Mason JC.

In the Western worldatherosclerosis is a more frequent cause of obstruction of the aortic arch vessels than Takyaasu arteritis. Check this box if you wish to receive a copy of your message. Goodpasture’s syndrome Sneddon’s syndrome. Coronal MRA shows an atypical aortic arch, with occlusion of the proximal segment of the left subclavian artery from its origin all the way to the emergence of the vertebral artery, with a filling of the distal subclavian bed.


Artérite de Takayasu — Wikipédia

Takayasu’s Arteritis in a Patient with Sydenham’s Chorea: The usual starting takayassu is approximately 1 milligram per kilogram of body weight per day for most people, this is approximately 60 milligrams a day.

Rev Bras Reumatol ;epub ahead of print. Angiography provides information on vessel anatomy and patency but does not provide information on the degree of inflammation in the wall. Summary and related texts. 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.

Ann Intern Med ; It is a condition, geographically more common in Southeast Asia, which mainly affects women of reproductive age. The patient improved in renal function with only intravenous hydration and was discharged with a creatinine of 2. Promising results are achieved with mycophenolate and tocilizumab [13]. During hospitalization, the patient was treated for hypothyroidism and was submitted to an abdominal ultrasound scan, which showed topical kidney, with normal morphology and echogenicity, with a slight reduction in the right kidney size, measuring 8.

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Clinical and statistical analyses of related prognostic factors” PDF. Takayasu’s arteritis is similar to other forms of vasculitis, including giant cell arteritis which typically affects older individuals.

Her laboratory tests did not stand out, with creatinine of 1.

arterite de Takayasu – Wiktionary

American Journal of Human Genetics. D ICD – This demonstrates the difficulty in diagnosis, and corroborates the fact that several recent studies have shown a high prevalence in the elderly.

Retrieved from ” https: The most commonly affected vessel is the subclavian artery, while renal artery stenosis is relatively uncommon.

Normally perfused kidneys produce a proportionate amount of a substance called renin. The clinical presentation is nonspecific, with signs and symptoms that vary according to the affected arterial segment. Fainting may result from subclavian steal syndrome or carotid sinus hypersensitivity.

The age at onset helps to differentiate Takayasu’s arteritis from other types of large vessel vasculitis.

Takayasu arteritis is a rare disease of unknown etiology that affects the aorta and its main branches. Renal revascularization in Takayasu arteritis-induced renal artery stenosis.