How long one lives with Buerger’s syndrome depends on the individual’s condition and can live up to 20 years or more if the disease is well controlled. The main symptoms include fever, right upper abdominal pain, rapid onset of massive pleural effusion, jaundice, tenderness in the liver, and oliguria. The main clinical method to confirm the diagnosis is angiography. Interventional surgery is preferred for Buga’s syndrome because it is less invasive and more effective, in addition to medical treatment. The main medical treatment of Buga’s syndrome mainly includes low-salt diet and nutritional support. Internal treatment can improve the patient’s general condition, reduce the mortality rate of surgery, and facilitate the patient’s recovery after surgery. Usually pay attention to their own maintenance, which can slow down the progress of the disease and improve the quality of life.