Fontan Operation in a Patient with Severe Hypoplastic Right Pulmonary Artery, Single Ventricle, and Heterotaxy Syndrome

被引:2
|
作者
Pan, Jun-Yen [1 ]
Lin, Chu-Chuan [2 ]
Chang, Jen-Ping [3 ]
机构
[1] Chang Gung Univ, Dept Cardiovasc Surg, Coll Med, Kaohsiung, Taiwan
[2] Chang Gung Univ, Dept Pediat, Coll Med, Kaohsiung Vet Gen Hosp, Kaohsiung, Taiwan
[3] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Coll Med, Dept Thorac & Cardiovasc Surg, Kaohsiung, Taiwan
关键词
Anomaly; Cardiovascular surgery; Congenital heart disease; HEMODYNAMICS; SIZE;
D O I
10.6515/ACS20160105A
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Assessment of the pulmonary circulation status including pressure, resistance, size, and absence of anatomical distortion, is crucial to the successful Fontan operation. Most patients are found to have acceptable pulmonary arteries after previous palliation, although some degree of distortion is not uncommon. However, in rare instances, some patients have only one functioning lung with another pulmonary artery seriously hypoplastic or atretic. For theses patients, completion of a Fontan operation will be challenging. We reported a 17-year-old girl with a single ventricle and heterotaxy syndrome and only her left lung functioning, who underwent one-lung Fontan operation with a satisfactory result.
引用
收藏
页码:612 / 615
页数:4
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