Feneley M P, Burns M W
Aust N Z J Med. 1983 Jun;13(3):280-2. doi: 10.1111/j.1445-5994.1983.tb04659.x.
Two cases in which cerebral abscess was the initial presenting feature of pulmonary arteriovenous malformations are reported. Cerebral abscess recurred in one patient. The pulmonary malformations were multiple and bilateral in both cases. One patient had associated features of hereditary hemorrhagic telangiectasia. Surgical resection of the largest malformations was performed in both cases. Cerebral abscess did not recur in either case post-operatively, though this may not have been due to surgical intervention.
报告了两例以脑脓肿为肺动静脉畸形初始表现特征的病例。其中一名患者脑脓肿复发。两例患者的肺部畸形均为多发且双侧性。一名患者伴有遗传性出血性毛细血管扩张症的相关特征。两例均对最大的畸形进行了手术切除。术后两例患者脑脓肿均未复发，不过这可能并非手术干预所致。
