Kokubo J, Koishizawa T, Tsuda K, Hayashi N, Ono M, Nonaka K, Fujiki T, Tonari K, Sasagawa N, Honda K
Department of the Thoracic and Cardiovascular Surgery, Kyorin University, School of Medicine, Tokyo, Japan.
Kyobu Geka. 1994 Mar;47(3):235-7.
This is a case report of 8-years-old boy, who was diagnosed mitral regurgitation, secundum type of atrial septal defect and annulo-aortic ectasia in association with Marfan syndrome. His diagnosis was confirmed at the age of 6 years when cardiac catheterization was carried out. Atrial septal defect was closed using PTFE patch (0.2 mm in thickness). His diseased mitral valve was replaced with CarboMedics prosthesis 27 mm in diameter. Because of intact aortic valvular function, we left the ectatic aorta alone at present time for future procedure. His postoperative course was uneventful. He is active and doing well at present and has been followed-up at the outpatient clinic routinely. He might be having to require AVR and graft implantation for ectatic ascending aorta.
这是一例8岁男孩的病例报告,该男孩被诊断为二尖瓣反流、继发孔型房间隔缺损以及与马方综合征相关的主动脉瓣环扩张。他在6岁时进行心导管检查后确诊。房间隔缺损使用厚度为0.2毫米的聚四氟乙烯补片闭合。其病变的二尖瓣被直径27毫米的CarboMedics人工瓣膜置换。由于主动脉瓣功能完好,目前我们暂未处理扩张的主动脉,留待未来进一步手术。他术后恢复过程顺利。他目前活动自如,情况良好,一直在门诊定期随访。他可能因升主动脉扩张而需要进行主动脉瓣置换术和移植物植入术。