Bou Prieto Elías, Canino Rodríguez Alexis, Martínez Toro José
Section of Cardiology, Department of Medicine, University of Puerto Rico School of Medicine, San Juan.
Bol Asoc Med P R. 2009 Oct-Dec;101(4):44-7.
Congenital structural abnormalities not associated with cyanosis may go undetected until late adulthood if clinical symptoms are not evident. We report the case of 17 year-old male, referred to cardiology clinics for evaluation of a murmur, which was found to have asymptomatic severe right heart chambers dilatation. Right heart catheterization and angiography revealed the diagnoses of partial anomalous pulmonary venous connection, an atrial septal defect and persistent left superior vena cava.
如果临床症状不明显,与非青紫相关的先天性结构异常可能直到成年后期才被发现。我们报告一例17岁男性病例,因杂音被转诊至心脏病诊所评估,结果发现其存在无症状的严重右心腔扩张。右心导管检查和血管造影显示诊断为部分性肺静脉异位连接、房间隔缺损和永存左上腔静脉。