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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Initial clinical manifestations can be insidious, with nonspecific signs and systemic symptoms, varying according to the affected arterial sites, and the left subclavian artery is ttakayasu one most often involved, followed by the aorta, the common carotid, the renal and the vertebral artery. AdultAdolescent ICD Some people develop an initial “inflammatory phase” characterized by systemic illness with signs and symptoms of malaisefevernight sweatsweight lossjoint painfatigueand fainting.

Her laboratory tests showed TSH Since then, the bearer of heart failure, atrial fibrillation, and dyslipidemia, without a diagnosis of hypertension SAH. Views Read Edit View history.

arterite de Takayasu

Summary and related texts. She was then referred to the nephrology clinic, where she was admitted for investigation. The age at onset helps to differentiate Takayasu’s arteritis from other types of large vessel vasculitis. Rev Bras Reumatol ;epub ahead of print.

We present in this report the case of an elderly arteite with late diagnosis of Takayasu’s arteritis and various comorbidities or related complications.

Her laboratory tests did not stand out, with creatinine of 1. Contrast angiography has been the gold standard. Angiography provides information on vessel anatomy and patency but does not provide information on the degree of inflammation in the wall. A hemodynamic study by means of ultrasonic Doppler flowmetry.


It mainly affects the aorta atrerite main blood vessel leaving the heart and its branches, as well as the pulmonary arteries. Renal-artery stenosis in a patient with Takayasu’s arteritis. Early endovascular experience for treatments of Takayasu’s arteritis. The clinical expression is varied and may be asymptomatic for several years, or present as nonspecific systemic symptoms such as fever, asthenia, arthralgia, myalgia or night sweats, and more rarely: Health care resources for this disease Takayasj centres Diagnostic tests 3 Patient organisations 23 Orphan drug s 0.

This demonstrates the difficulty in diagnosis, and corroborates the fact that several recent studies have shown a high prevalence in the elderly. Imaging findings in Takayasu’s arteritis. Mesut; Guthridge, Joel M. Goodpasture’s syndrome Sneddon’s syndrome.

A sixty-five year-old female, born and living in Pelotas, a former smoker, with a previous history of mitral valve disease due to rheumatic fever sequelae, withs replacement by bioprosthesis for 9 years. J Vasc Surg ; In other projects Wikimedia Commons.

arterite de Takayasu – Wiktionary

Frontiers in Cardiovascular Medicine. She continued under medical care at a basic healthcare unit in her own district, takayask she used to present nonspecific symptoms such as fatigue, diffuse arthralgia, dizziness, intermittent claudication, diffuse myalgia, tachycardia, and depressive symptoms. A large collaborative study uncovered multiple additional susceptibility loci for this disease, ee its number of genetic loci to five risk loci across the genome.

Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s Takayasu’s Arteritis in a Patient with Sydenham’s Chorea: Only comments written in English can be processed. Check this box if you wish to receive a copy of your message.


The patient improved in renal function with only intravenous hydration and was discharged with a creatinine of 2. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis takayaeu diagnosis or treatment.

American Journal of Human Genetics.

Artérite de Takayasu

As with all aneurysms, the possibility of rupture and vascular bleeding is existent and requires monitoring. The clinical presentation is nonspecific, with signs and symptoms that vary according to the affected arterial segment. Chronic and slow-developing TA -the arterit 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.

Diagnosis is based on the demonstration of vascular lesions in large arterte middle-sized vessels on angiography, CT scanmagnetic resonance angiography or FDG PET. Takayasu arteritis TA is arteritf rare chronic granulomatous inflammatory arterial disease of unknown etiology that may affect the aorta and its main branches. From Wikipedia, the free encyclopedia.