Haitjema T, ten Berg J M, Overtoom T T, Ernst J M, Westermann C J
Department of Pulmonology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Chest. 1996 May;109(5):1401-4. doi: 10.1378/chest.109.5.1401.
A pulmonary arteriovenous malformation was embolized in a patient with hereditary hemorrhagic telangiectasia. Several unusual complications, including early deflation of a detachable balloon, migration of a coil, and development of severe pulmonary hypertension, occurred. Pulmonary hypertension was attributed to a coexistent left-to-right shunt caused by a large hepatic arteriovenous malformation.
一名患有遗传性出血性毛细血管扩张症的患者的肺动静脉畸形接受了栓塞治疗。出现了几种不寻常的并发症，包括可脱卸球囊早期瘪陷、弹簧圈移位以及严重肺动脉高压的发生。肺动脉高压归因于同时存在的由巨大肝动静脉畸形导致的左向右分流。
