Division of Cardiovascular Surgery, Department of Surgery, Shiga University of Medical Science, Otsu, Japan.
Eur J Cardiothorac Surg. 2019 Sep 1;56(3):622-624. doi: 10.1093/ejcts/ezy487.
Löffler endocarditis with hypereosinophilic syndrome is rare but can cause critical ventricular obliteration by endomyocardial fibrosis. A 52-year-old woman experienced severe right heart failure with extreme shrinkage of her right ventricle, severe tricuspid regurgitation and marked right atrial enlargement. Preoperative tests showed identical pressures in the right atrium and pulmonary artery. Endocardial stripping was done, and to enlarge the right ventricle, we relocated the anterior and posterior tricuspid leaflets cephalad, up the right atrium wall, to 'ventricularize' a portion of the right atrium, with autologous pericardial augmentation of the tricuspid leaflets. An annuloplasty ring was added to reinforce the relocated tricuspid attachment. Right heart pressures normalized postoperatively. The patient recovered uneventfully. She has received corticosteroid therapy continuously and has shown no recurrence of heart failure in the 5 years since surgery.
罗弗勒心内膜炎伴嗜酸性粒细胞增多综合征较为罕见,但可引起心内膜心肌纤维化导致严重的心室闭塞。一位 52 岁女性因严重的右心衰竭就诊,其右心室极度缩小,三尖瓣重度反流,右心房显著扩大。术前检查显示右心房和肺动脉压力相同。我们进行了心内膜剥离术,为了扩大右心室,我们将前后三尖瓣瓣叶向头侧、沿右心房壁向上移位,将部分右心房“心室化”,并用自体心包片增强三尖瓣瓣叶。加一个瓣环成形环以加强重新定位的三尖瓣附着点。术后右心压力恢复正常。患者恢复顺利。她持续接受皮质类固醇治疗,手术后 5 年心力衰竭未再复发。