Looyenga D S, Lacina S J, Gebuhr C J, Stockinger F S
J Am Coll Cardiol. 1986 Sep;8(3):621-6. doi: 10.1016/s0735-1097(86)80192-9.
A 14 year old white girl who presented with a brain abscess was discovered to have a left pulmonary vascular malformation on a chest roentgenogram. Angiograms revealed a left superior vena cava that drained into a venous malformation within the left lung, then communicated with the left atrium by way of the left superior pulmonary vein. The right superior vena cava was functionally absent and was anatomically an atretic cord. There was mild systemic arterial hemoglobin desaturation, but no evidence of cyanosis. The embryology, physiology and surgical repair of this rare lesion and the complication of a postoperative superior vena cava syndrome are discussed.
一名14岁白人女孩因脑脓肿就诊,胸部X线片发现左肺血管畸形。血管造影显示左上腔静脉引流至左肺内的静脉畸形,然后通过左上肺静脉与左心房相通。右上腔静脉功能缺失,解剖上为闭锁索条。有轻度全身动脉血红蛋白饱和度降低,但无发绀证据。本文讨论了这种罕见病变的胚胎学、生理学、手术修复及术后上腔静脉综合征并发症。