摘要Takayasu arteritis (TA) is a chronic progressive nonspecific vasculitis that involves the aorta and its main branches,resulting in luminal stenosis in the large vessels.Steroid therapy is the foundation for TA treatment and the guarantee of surgery.When a patient presents with uncontrolled symptoms,surgical treatment is the only measure that may be adopted to prevent greater risk to life.However,surgical repair for extensive arteriopathy requires an ingenious design to avoid morbidity in response to the complexity of the pathophysiology of TA.A 41-year-old woman presented with pulselessness,recurrent dizziness,and visual disturbance for the past 23 years.The patient had been diagnosed with TA 13 years ago and had received steroid therapy.However,the symptoms of dizziness and visual disturbance had increased in intensity and duration over the last 2 years.