Sadiq M, Sreeram N, de Giovanni J V, Wright J G, Brawn W J, Ladusans E J, Sethia B
Heart Unit, Birmingham Children's Hospital, United Kingdom.
Ann Thorac Surg. 1995 Mar;59(3):753-5. doi: 10.1016/0003-4975(94)00578-8.
An 8-year-old boy who suffered from Hirschsprung's disease had development of tricuspid valve endocarditis that progressed to aortic root abscess formation, development of a fistulous communication between aorta and right atrium, atrial and ventricular septal defects, and a left ventricle to right atrium defect. Several surgical procedures were required. Operation consisted initially of closure of the septal defects and aortic valve repair. This was followed by homograft replacement of the aortic valve for persistent infection, and further closure of a left ventricle to right atrium fistula.
一名患有先天性巨结肠症的8岁男孩患上了三尖瓣心内膜炎,病情进展为主动脉根部脓肿形成、主动脉与右心房之间出现瘘管交通、房间隔和室间隔缺损以及左心室至右心房缺损。需要进行多次外科手术。手术最初包括闭合间隔缺损和修复主动脉瓣。随后因持续感染进行了主动脉瓣同种异体移植置换,并进一步闭合了左心室至右心房瘘。