Itaoka Y, Katou A, Kurihara H, Hara K, Takeuchi H, Degawa T, Kuwako K, Yamaguchi T, Akiyama Y, Miyamoto H
Center for Cardiovascular Diseases, Mitsui Memorial Hospital.
Kokyu To Junkan. 1990 Aug;38(8):811-4.
We report a case of a 59-year-old male who suddenly developed massive right hemothorax and shock due to pulmonary arteriovenous malformation (AVM). He was admitted as an emergency case because of severe back pain, cyanosis and cold sweat. Although shock with massive right hemothorax was found, echocardiographic and X-ray computed tomographic examination showed no dilatation of the aorta, no intimal flap in the aorta and no pericardial effusion which suggested aneurysm. Pulmonary arteriography, performed subsequently, disclosed intrapleural rupture of the right pulmonary AVM. The patient recovered successfully from the state of shock. The pulmonary AVM was removed by segmentectomy of the right lung (S4). He was discharged following an uneventful postoperative course. Intrapleural rupture with shock is a very rare complication of pulmonary AVM. Pulmonary AVM should be considered as one possible cause in patients with massive hemothorax and shock.
我们报告一例59岁男性,因肺动静脉畸形(AVM)突然出现大量右侧血胸并休克。他因严重背痛、发绀和冷汗作为急诊入院。尽管发现有大量右侧血胸伴休克,但超声心动图和X线计算机断层扫描检查显示主动脉无扩张,主动脉内无内膜瓣,也无提示动脉瘤的心包积液。随后进行的肺动脉造影显示右侧肺AVM胸膜内破裂。患者成功从休克状态中恢复。通过右肺(S4)段切除术切除了肺AVM。术后过程平稳,患者出院。伴有休克的胸膜内破裂是肺AVM非常罕见的并发症。对于出现大量血胸和休克的患者,应将肺AVM视为一种可能的病因。