Kallfelz H C, Borst H G
Thoraxchir Vask Chir. 1975 Jun;23(3):238-42. doi: 10.1055/s-0028-1096954.
Pulmonary arteriovenous fistula is not a rare congenital malformation, but obviously most often it is a very late diagnosis. Moreover the disease is associated with a high risk of serious complications, namely cerebrovascular accidents. Two patients, an one month old infant and an 8 years old boy with typical symptoms and signs are presented. Both of them were operated upon successfully. It is concluded, that the diagnosis of solitary pulmonary arteriovenous fistula should lead to immediate operation, which is technically easy and of low risk only, even in infancy. Conservative surgery is recommended without sacrifice of healthy lung tissue, i.e. local excision or segmental resection in subpleural lesions and lobectomy for deep-seated fistulas.
肺动静脉瘘并非罕见的先天性畸形,但显然大多数情况下诊断都很晚。此外,该疾病伴有严重并发症的高风险,即脑血管意外。本文介绍了两名患者,一名1个月大的婴儿和一名8岁男孩,他们都有典型的症状和体征。两人均成功接受了手术。得出的结论是,孤立性肺动静脉瘘一旦诊断应立即手术,即使在婴儿期,手术在技术上也很简单且风险很低。建议采用保守手术,不牺牲健康肺组织,即对胸膜下病变进行局部切除或节段性切除,对深部瘘管进行肺叶切除。