Liberthson R R, Miller S W, Drew F, Palacios I, Singh J
Cardiovasc Intervent Radiol. 1981;4(2):131-5. doi: 10.1007/BF02552393.
Congenital extracardiac shunts in tetralogy of Fallot may significantly alter the history and clinical findings and also have significant management implications. An unusual variant of severe tetralogy of Fallot in a 54-year-old man enabled long survival with minimal symptoms. The patient had pulmonary valvular and infundibular stenosis, a large ventricular septal defect, an overriding aorta, and large volume systemic-to-pulmonary artery shunting from his right internal mammary and accessory internal mammary arteries to his right pulmonary artery.
法洛四联症中的先天性心外分流可能会显著改变病史和临床检查结果,并且在治疗方面也有重要意义。一名54岁男性患有严重法洛四联症的罕见变异型,症状轻微,生存期长。该患者存在肺动脉瓣和漏斗部狭窄、大型室间隔缺损、主动脉骑跨,以及从右胸廓内动脉和胸廓内副动脉到右肺动脉的大量体肺分流。