Frankel Agustina, Ferris Rebekah, Hodgkinson Peter, Ellender Claire M
Department of Respiratory & Sleep Medicine Princess Alexandra Hospital Woolloongabba QLD Australia.
Respirol Case Rep. 2020 Mar 8;8(3):e00543. doi: 10.1002/rcr2.543. eCollection 2020 Apr.
Pulmonary arteriovenous malformations are common in patients with hereditary haemorrhagic telangiectasia and can be associated with significant hypoxia and intra-pulmonary shunt. We present a case of a young man with a known 57% calculated shunt requiring abdominal surgery and the multidisciplinary decisions required in the preoperative period to minimize post-operative complications.
肺动静脉畸形在遗传性出血性毛细血管扩张症患者中很常见,并且可能与严重缺氧和肺内分流有关。我们报告一例已知分流率为57%的年轻男性患者,该患者需要接受腹部手术,以及术前为尽量减少术后并发症而做出的多学科决策。