Takayasu's動脈炎症,在臨床病例並不多見,好發於年青女性,常侵犯主動脈及其分枝之血管,為一種原因不明之非特異性血管炎症變化。其合併纖雜化病變時,可增厚管壁,造成血管阻塞,狹窄或產生動脈瘤等變化。臨床症狀為由血管阻塞所造成續發症狀之表現,其診斷主要靠放射線動脈血管攝影術來鑑別。本文提出本症有關之數據及病例說明之。
Takayasu's arteritis is a rare disease and predominated in young females. This disease usually involve aorta and it's main branches, such as subclavian, carotid and renal arteries. The etiology of T.A. is unknown with pathological picture of non-specific arteritis. The clinic manifestation is characterized by the Secondary symptoms of vascular occlusion and stenosis. The diagnosis is based on angiographic examination. The angiographic finding in Takayasu's arteritis include occlusive disease, aneurysmal changes or combination of two. Here we reported two cases and illustration.