Ungaro R, Saab S, Almond C H, Kumar S
J Thorac Cardiovasc Surg. 1976 Apr;71(4):566-71.
The case of a solitary peripheral pulmonary artery aneurysm in a patient with congenital heart disease and secondary pulmonary hypertension is presented. The aneurysm appeared following an episode of bacterial endocarditis and was probably mycotic in origin. Resection was prompted by a recent increase in size. A successful aneurysmectomy was performed. Lobectomy was the procedure employed in seven other reported cases treated surgically. A brief review of the literature emphasizes the necessity for resection whenever the diagnosis is made to prevent a fatal outcome due to rupture. A classification of pulmonary artery aneurysms based on their etiology is proposed, together with a possible explanation for the pathogenesis of peripheral aneurysms of nonspecific etiology.
本文报告了一例先天性心脏病合并继发性肺动脉高压患者的孤立性外周肺动脉瘤病例。该动脉瘤在细菌性心内膜炎发作后出现,可能起源于真菌。近期瘤体增大促使进行手术切除。成功实施了动脉瘤切除术。在其他七例报告的手术治疗病例中采用的是肺叶切除术。文献简要回顾强调,一旦做出诊断,为防止因破裂导致致命后果,进行切除手术很有必要。本文提出了基于病因的肺动脉瘤分类方法,以及对非特异性病因外周动脉瘤发病机制的一种可能解释。