Zhang Jing, Huang Zhi-Xiong, Sun Han-Song, Luo Xin-Jin, Xu Jian-Ping
Department of Cardiovascular Surgery, Fu Wai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China.
Zhonghua Wai Ke Za Zhi. 2009 Jun 1;47(11):845-8.
To analyze symptoms, associated anomalies, diagnostic approach, and surgical procedures in patients with unroofed coronary sinus syndrome and atrioventricular canal defect.
The clinical data of 20 patients with unroofed coronary sinus syndrome from September 1999 to October 2007 were reviewed retrospectively. There were 10 male and 10 female patients. The age ranged from 6 months to 38 years old, with a mean of (11.4 +/- 11.0) years old. The body weight ranged from 6.7 to 73.0 kg, with a mean of (28.4 +/- 21.3) kg. There were 18 cases of partial atrioventricular canal defect, 2 cases of complete atrioventricular canal defect, and 12 cases of common atrium. The initial diagnosis of unroofed coronary sinus syndrome was made by the surgeon at repair of a partial or complete atrioventricular canal defect in 20 patients. Complex unroofed coronary sinus with left superior vena cava (LSVC) directly draining into the left atrium was found in 11 cases, 1 case of LSVC was ligated, 10 cases were reconstructed the intraatrial baffle or the intracardiac tunnel to drain LSVC to right atrium. The other 9 patients with simple unroofed coronary sinus were repaired with other procedures. The associated cardiac lesions were corrected concomitantly.
Death occurred in 1 patient with complex congenital cardiac disease due to pulmonary infection. In the 14 early survivors, who had been followed up from 4 months to 3 years, there was no death and severe complications.
When associated with a partial or complete atrioventricular canal defect, LSVC and a common atrium, unroofed coronary sinus syndrome should be considered as a possible additional finding. Repair according to the type of unroofed coronary sinus syndrome is effective.
分析无顶冠状静脉窦综合征合并房室管缺损患者的症状、相关异常、诊断方法及手术操作。
回顾性分析1999年9月至2007年10月期间20例无顶冠状静脉窦综合征患者的临床资料。其中男性10例,女性10例。年龄6个月至38岁,平均(11.4±11.0)岁。体重6.7至73.0千克,平均(28.4±21.3)千克。部分房室管缺损18例,完全房室管缺损2例,共同心房12例。20例患者在修补部分或完全房室管缺损时由外科医生初步诊断为无顶冠状静脉窦综合征。发现11例复杂型无顶冠状静脉窦合并左上腔静脉(LSVC)直接引流至左心房,1例结扎LSVC,10例重建心房内挡板或心内隧道将LSVC引流至右心房。另外9例单纯无顶冠状静脉窦患者采用其他手术方法修补。同时矫正相关心脏病变。
1例复杂先天性心脏病患者因肺部感染死亡。14例早期存活患者随访4个月至3年,无死亡及严重并发症。
当合并部分或完全房室管缺损、LSVC及共同心房时,应考虑有无顶冠状静脉窦综合征这一可能的额外发现。根据无顶冠状静脉窦综合征类型进行修补有效。