RELATO DE CASO: ARTERITE DE TAKAYASU.

Takayasu arteritis is a rare systemic vasculitis, characterized by the involvement of large vessels, mainly the aorta and its branches. The diagnosis is based on the suggestive clinical condition, complementary tests and the criteria of the American College of Rheumatology. Treatment is based on high doses of glucocorticoids and disease-modifying agents such as methotrexate, azathioprine, and cyclophosphamide. The aim of this study is to report a case of Takayasu's arteritis in a female patient, with extensive vascular involvement and classic manifestations of the disease. The patient was treated with high doses of corticosteroids and cyclophosphamide, followed by maintenance treatment with methotrexate. Knowing the disease is crucial to avoid late diagnosis and reduce morbidity and mortality. Treatment must always be individualized, based on side effects and availability of each medication, as well as the experience of the prescribing professional. [ABSTRACT FROM AUTHOR]