Kuwaki K, Morishita K, Sato H, Urita R, Abe T
Departments of Thoracic and Cardiovascular Surgery, Sapporo Medical University School of Medicine, South 1, West 16, Chuo-ku, 060-0061, Sapporo, Japan.
Eur J Cardiothorac Surg. 2000 Nov;18(5):535-9. doi: 10.1016/s1010-7940(00)00568-6.
Aneurysm formation of the pulmonary trunk is rare and there is controversy about optimal treatment for this disease. The aim of this article is to report four patients with pulmonary trunk aneurysm which were managed by surgical repair.
From 1986 to 1997, we performed surgical repair for pulmonary trunk aneurysm in four patients. There was one male and three female patients with a mean age of 63.3 years (range: 54-78 years). Concomitant diseases were cardiac valvular disease in four patients, thoracic aortic dissection in two, atherosclerotic abdominal aortic aneurysm in two, and coronary artery disease in one. All patients were in New York Heart Association functional class III preoperatively. Surgical procedures for the pulmonary trunk aneurysm included Dacron graft replacement in two patients and aneurysmorrhaphy in two. Associated procedures were cardiac valvular operation in three patients with four lesions and right ventricular outflow tract reconstruction (RVOTR) in one.
There were no operative mortalities and no late deaths with a mean follow-up period of 6.6 years (range: 2.4-10.0 years). One female patient developed recurrent pulmonary trunk aneurysm 9.5 years after aneurysmorrhaphy, and underwent a second operation where Dacron graft replacement of the aneurysm including pulmonary valve replacement was performed successfully. All patients are now leading normal lives.
Surgical management should be considered for large aneurysm of the pulmonary trunk regardless of its etiology and underlying disease to prevent possible rupture with fatal result if the patient has an acceptably low operative risk.
肺动脉干动脉瘤形成较为罕见,对于该疾病的最佳治疗方法存在争议。本文旨在报告4例接受手术修复治疗的肺动脉干动脉瘤患者。
1986年至1997年,我们对4例肺动脉干动脉瘤患者进行了手术修复。其中男性1例,女性3例,平均年龄63.3岁(范围:54 - 78岁)。合并疾病包括4例患者有心脏瓣膜病,2例有胸主动脉夹层,2例有动脉粥样硬化性腹主动脉瘤,1例有冠状动脉疾病。所有患者术前均为纽约心脏协会心功能Ⅲ级。肺动脉干动脉瘤的手术方式包括2例患者行涤纶补片置换术,2例患者行动脉瘤缝合术。相关手术包括3例合并4处病变的患者行心脏瓣膜手术,1例患者行右心室流出道重建术(RVOTR)。
平均随访6.6年(范围:2.4 - 10.0年),无手术死亡病例,也无晚期死亡病例。1例女性患者在动脉瘤缝合术后9.5年出现复发性肺动脉干动脉瘤,接受了第二次手术,成功进行了包括肺动脉瓣置换在内的动脉瘤涤纶补片置换术。所有患者目前均过着正常生活。
对于肺动脉干大动脉瘤,无论其病因和基础疾病如何,如果患者手术风险可接受,为防止可能的破裂导致致命后果,应考虑手术治疗。