Fukuoka Kentoku, Aizawa Kei, Sugaya Akira, Kawada Masaaki, Kawahito Koji
Department of Cardiothoracic Surgery, Jichi Medical University, Shimotsuke, Japan.
Kyobu Geka. 2018 Dec;71(13):1088-1091.
Pulmonary artery aneurysm (PAA) is usually associated with congenital heart disease, pulmonary artery hypertension, and connective tissue abnormalities, but idiopathic PAA is a rare clinical entity. We experienced a surgical case of idiopathic PAA measuring 60 mm in diameter. A 72-year-old man had been admitted to a nearby hospital 5 years before because of an abnormal shadow on chest X-ray, and was diagnosed with an idiopathic PAA measuring 37 mm in diameter. The PAA gradually expanded during follow-up and surgery was scheduled. Aneurysmal resection and reconstruction with a 24 mm expanded polytetrafluoroethylene graft were performed. The postoperative course was uneventful and the patient was discharged on the 11th postoperative day.
肺动脉瘤(PAA)通常与先天性心脏病、肺动脉高压和结缔组织异常有关,但特发性PAA是一种罕见的临床病症。我们遇到了一例直径为60毫米的特发性PAA的手术病例。一名72岁男性在5年前因胸部X光片上的异常阴影入住附近医院,被诊断为直径37毫米的特发性PAA。在随访期间,PAA逐渐扩大,遂安排手术。采用24毫米的膨体聚四氟乙烯移植物进行了动脉瘤切除和重建。术后过程顺利,患者在术后第11天出院。