Sharma Awadhesh Kr, Nath Ranjit Kumar, Pandit Neeraj
DM 3rd yr, Senior Resident, Department of Cardiology, PGIMER & Dr Ram Manoher Lohia Hospital, New Delhi 110001, India.
DM, Professor, Department of Cardiology, PGIMER & Dr Ram Manoher Lohia Hospital, New Delhi 110001, India.
Hellenic J Cardiol. 2016 Mar-Apr;57(2):124-8. doi: 10.1016/j.hjc.2016.03.005. Epub 2016 Apr 5.
We present a case of sinus venosus atrial septal defect in a patient who was previously diagnosed as having primary pulmonary hypertension in a tertiary care center. Our findings are based on 2-dimensional trans-thoracic echocardiography, chest X-ray and surface electrocardiogram. A 26-year-old man, previously diagnosed as a case of primary pulmonary hypertension, presented to the emergency department (ED) with chest pain and breathlessness on exertion. Cardiac biomarkers were within their normal ranges. Surface electrocardiogram showed right atrial and ventricular overload with right axis deviation. Chest imaging noted enlarged central pulmonary vascularity with bilateral plethoric lung fields. Trans-thoracic echocardiography showed a dilated right atria and ventricle with severe tricuspid regurgitation and severe pulmonary artery hypertension with an intact atrial septum. Surprisingly, the transoesophageal echocardiogram revealed the presence of a sinus venous superior vena cava-type atrial septal defect with the right pulmonary vein draining into the right atria. In this full-text version, we present a more detailed discussion of sinus-venous atrial septal defect associated with partial anomalous pulmonary venous return that was wrongly diagnosed as a case of primary pulmonary hypertension in a tertiary care center.
我们报告一例窦静脉型房间隔缺损患者,该患者先前在一家三级医疗中心被诊断为原发性肺动脉高压。我们的诊断基于二维经胸超声心动图、胸部X线和体表心电图检查结果。一名26岁男性,先前被诊断为原发性肺动脉高压,因胸痛和劳力性呼吸困难就诊于急诊科(ED)。心脏生物标志物在正常范围内。体表心电图显示右心房和心室负荷过重伴电轴右偏。胸部影像学检查发现中央肺血管增粗,双侧肺野充血。经胸超声心动图显示右心房和右心室扩大,伴有严重的三尖瓣反流和严重的肺动脉高压,房间隔完整。令人惊讶的是,经食管超声心动图显示存在窦静脉上腔静脉型房间隔缺损,右肺静脉引流至右心房。在本全文版本中,我们对与部分性肺静脉异位引流相关的窦静脉型房间隔缺损进行了更详细的讨论,该患者在一家三级医疗中心被误诊为原发性肺动脉高压。