Pasic M, von Segesser L, Carrel T, Arbenz U, Tönz M, Niederhäuser U, Vogt P, Turina M
Clinic for Cardiovascular Surgery, University Hospital Zurich, Switzerland.
Cardiovasc Surg. 1993 Oct;1(5):608-12.
Between 1977 and 1992, four infants with an anomalous left pulmonary artery and subsequent compression of the tracheobronchial tree were operated on at the University Hospital Zurich. The operation consisted of mobilization of the abnormal left pulmonary artery with reimplantation into the main pulmonary trunk in three patients; the left pulmonary artery was transected and restored in front of the trachea by end-to-end anastomosis in one. Mean follow-up was 7 years (range 2 months to 14.3 years). There were no early and no late deaths. All patients have shown significant symptomatic improvement without respiratory infection or disturbance of normal life activities. Surgical therapy in this rare condition can be safely undertaken with good long-term results. In symptomatic patients the operation should be performed early before occurrence of severe respiratory symptoms and bronchial collapse.
1977年至1992年间,苏黎世大学医院为4例左肺动脉异常并随后出现气管支气管树受压的婴儿实施了手术。手术包括3例将异常左肺动脉游离并重新植入主肺动脉干;1例将左肺动脉在气管前方切断并通过端端吻合进行修复。平均随访7年(范围2个月至14.3年)。无早期和晚期死亡病例。所有患者症状均有显著改善,无呼吸道感染,正常生活活动未受干扰。这种罕见疾病的手术治疗可安全进行,且长期效果良好。对于有症状的患者,应在出现严重呼吸道症状和支气管塌陷之前尽早进行手术。