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Ross手术后的二叶式主动脉瓣疾病与肺动脉自体移植根部扩张:一项临床病理研究。

Bicuspid aortic valve disease and pulmonary autograft root dilatation after the Ross procedure: a clinicopathologic study.

作者信息

Luciani G B, Barozzi L, Tomezzoli A, Casali G, Mazzucco A

机构信息

Division of Cardiac Surgery, University of Verona, Verona, Italy.

出版信息

J Thorac Cardiovasc Surg. 2001 Jul;122(1):74-9. doi: 10.1067/mtc.2001.114638.

Abstract

OBJECTIVE

Bicuspid aortic valve disease has been associated with histologic abnormalities of the aortic root. Recent reports have suggested similar alterations may exist in the pulmonary artery of patients with bicuspid aortic valve. The present study was undertaken to define the histologic condition of the aortic and pulmonary artery root in bicuspid aortic valve disease and the relationship with pulmonary autograft root dilatation after the Ross procedure.

METHODS

In 17 patients undergoing aortic root replacement with the pulmonary autograft, biopsy specimens of the aortic root and pulmonary artery trunk were collected. Clinical and histologic findings of patients with bicuspid aortic valves were compared with those with tricuspid aortic valves.

RESULTS

There were 9 patients (8 male, 1 female) with bicuspid aortic valve (group 1) and 8 (all male) with tricuspid aortic valve (group 2). Mean age was comparable (24.4 +/- 9.8 vs 23.6 +/- 10.8 years, P =.9). Aortic insufficiency as an indication for operation was more common in group 1 (9/9 vs 5/8, P =.007), whereas preoperative aortic root dilatation was equally prevalent (4/9 vs 1/8, P =.1). Prior aortic valve repair had been performed in 2 patients (1/9 vs 1/8, P =.9). Prevalence of cystic medionecrosis of the aortic wall was similar in the 2 groups (4/9 vs 3/8, P =.6). Cystic medionecrosis of the pulmonary artery trunk was found only in 1 patient with tricuspid aortic valve (0/9 vs 1/8, P =.3). During a mean follow-up of 26.5 +/- 12.2 months (32.1 +/- 12.7 vs 20.1 +/- 7.4 months, P =.04), prevalence of pulmonary autograft root dilatation (greater than 4.0 cm) was equally represented in patients with native bicuspid or tricuspid aortic valve (3/9 vs 2/8, P =.6).

CONCLUSIONS

Histologic abnormalities of the pulmonary artery root are rare and equally prevalent in young patients with bicuspid and tricuspid aortic valves. On the contrary, root dilatation is relatively common late after autograft root replacement but appears unrelated to bicuspid aortic valve disease or to pre-existing degenerative changes of the pulmonary artery root.

摘要

目的

二叶式主动脉瓣疾病与主动脉根部的组织学异常有关。最近的报告表明,二叶式主动脉瓣患者的肺动脉可能存在类似改变。本研究旨在明确二叶式主动脉瓣疾病患者主动脉和肺动脉根部的组织学状况,以及与Ross手术后肺动脉自体移植根部扩张的关系。

方法

对17例行肺动脉自体移植主动脉根部置换术的患者,采集主动脉根部和肺动脉主干的活检标本。将二叶式主动脉瓣患者的临床和组织学结果与三叶式主动脉瓣患者进行比较。

结果

二叶式主动脉瓣患者9例(男8例,女1例)(第1组),三叶式主动脉瓣患者8例(均为男性)(第2组)。平均年龄相当(24.4±9.8岁 vs 23.6±10.8岁,P = 0.9)。作为手术指征的主动脉瓣关闭不全在第1组更常见(9/9 vs 5/8,P = 0.007),而术前主动脉根部扩张同样普遍(4/9 vs 1/8,P = 0.1)。2例患者曾行主动脉瓣修复术(1/9 vs 1/8,P = 0.9)。两组主动脉壁囊性中层坏死的发生率相似(4/9 vs 3/8,P = 0.6)。仅1例三叶式主动脉瓣患者发现肺动脉主干囊性中层坏死(0/9 vs 1/8,P = 0.3)。平均随访26.5±12.2个月(32.1±12.7个月 vs 20.1±7.4个月,P = 0.04),先天性二叶式或三叶式主动脉瓣患者肺动脉自体移植根部扩张(大于4.0 cm)的发生率相当(3/9 vs 2/8,P = 0.6)。

结论

肺动脉根部的组织学异常罕见,在年轻的二叶式和三叶式主动脉瓣患者中同样普遍。相反,自体移植根部置换术后晚期根部扩张相对常见,但似乎与二叶式主动脉瓣疾病或肺动脉根部先前存在的退行性改变无关。

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