Barbara David W, Edwards William D, Connolly Heidi M, Dearani Joseph A
Mayo Medical School, Mayo Clinic, Rochester, MN 55905, USA.
Cardiovasc Pathol. 2008 May-Jun;17(3):166-71. doi: 10.1016/j.carpath.2007.07.005. Epub 2007 Oct 24.
Ebstein's anomaly has been described extensively in autopsy material. However, there have been no large surgical pathology series of this malformation.
To review clinical and surgical pathologic features of a large number of cases of Ebstein's anomaly from a single institution.
Review of medical histories, surgical reports, and surgical pathology reports at the Mayo Clinic (2000-2005).
Among 104 patients, the mean age was 31 years (2 months-79 years), and 57% were female. Common ECG abnormalities included right bundle branch block (58%), first-degree heart block (31%), preexcitation (18%), and nonspecific intraventricular conduction delay/block (15%). Moreover, 74% had inter-atrial communication, 13% mitral valve prolapse, and 5% bicuspid aortic valve. Clinically, all had tricuspid regurgitation (severe in 74%), and 17% of anterior leaflets were fenestrated. No tricuspid valve was calcified. Surgically, tricuspid tissue was removed during replacement in 99% and repair in 1%. The anterior tricuspid leaflet was resected in 98%, and its length was 0.81-9.3 cm/m2 body surface area (mean, 3.3). Characteristically, leaflets were large and had irregular shapes and numerous short cordal or direct myocardial insertions. One tricuspid valve had two papillary fibroelastomas. None had clinical or pathologic evidence of active or healed endocarditis.
Among patients with Ebstein's malformation, tricuspid valve tissue almost exclusively was removed during valve replacement and represented the anterior leaflet. Valve tissue was generally large, irregularly shaped, and associated with insertion of short cords or myocardial stumps. Interestingly, although appreciably deformed, Ebstein valves were not associated with infective endocarditis.
埃布斯坦畸形在尸检材料中有广泛描述。然而,尚无关于这种畸形的大型外科病理学系列研究。
回顾来自单一机构的大量埃布斯坦畸形病例的临床和外科病理特征。
回顾梅奥诊所(2000 - 2005年)的病史、手术报告和手术病理报告。
104例患者中,平均年龄为31岁(2个月至79岁),57%为女性。常见的心电图异常包括右束支传导阻滞(58%)、一度房室传导阻滞(31%)、预激(18%)和非特异性室内传导延迟/阻滞(15%)。此外,74%有房内交通,13%有二尖瓣脱垂,5%有二叶式主动脉瓣。临床上,所有患者均有三尖瓣反流(74%为重度),17%的前叶有穿孔。无三尖瓣钙化。手术方面,99%的患者在瓣膜置换时切除了三尖瓣组织,1%进行修复。98%切除了三尖瓣前叶,其长度为0.81 - 9.3 cm/m²体表面积(平均3.3)。其特征是瓣膜叶大、形状不规则且有许多短腱索或直接心肌附着。一个三尖瓣有两个乳头纤维弹性瘤。均无活动性或愈合性心内膜炎的临床或病理证据。
在埃布斯坦畸形患者中,瓣膜置换时几乎都切除了三尖瓣组织,且为前叶。瓣膜组织通常较大、形状不规则,并伴有短腱索或心肌残端附着。有趣的是,尽管埃布斯坦瓣膜明显变形,但与感染性心内膜炎无关。