Mortezaeian Hojjat, Jafari Farshad, Meraji Mahmoud, Tabib Avisa, Pouraliakbar Hamid Reza, Naderi Fatemeh
Rajaie Cardiovascular Medical & Research Center, Iran University of Medical Sciences, Tehran, Iran.
Heart Valve Disease Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Int J Emerg Med. 2024 Nov 25;17(1):179. doi: 10.1186/s12245-024-00770-7.
Cyanotic congenital heart diseases are among the most serious anomalies among newborns. A rare type of this condition is direct communication between the right pulmonary artery and left atrium, which presents mostly in adolescence and adulthood. Large shunts, however, should be corrected as soon as possible, considering their potential to cause congestive heart failure.
Two 2- and 13-year-old patients with this pathologic communication complained of exertional dyspnea and central cyanosis. Their physical exams were prominent, with a low oxygen saturation level. The diagnostic modalities used, electrocardiogram, chest X-ray, echocardiogram, CT scan, and selective angiography of the pulmonary arteries, showed right-to-left abnormal blood flow through the right pulmonary artery and left atrium shunt. Finally, both patients were treated successfully by a transcatheter occluder without any complications or follow-up complaints.
The right pulmonary artery and left atrium abnormal congenital connections are rare causes of central cyanosis, mostly present with exertional dyspnea and cyanosis during adolescence or early adulthood. Transthoracic echocardiography, contrast-enhanced CT scans, and angiography of the pulmonary arteries make the diagnosis. The treatment has emerged during the last two decades, shifting from surgical treatment for severe cases to interventional percutaneous strategies, leaving the surgery for cases with no appropriate location for the application of interventional therapy.
Considering the potentially life-threatening complications of the untreated right pulmonary artery and left atrium fistulas, such as thromboembolic events, early diagnosis is crucial. However, treating these patients is not always straightforward, and strategies should be selected based on the connecting fistula's anatomical features, location, size, and tortuosity. Although endovascular treatment is the preferred option, some patients need to be treated with surgical procedures due to their structural characteristics.
青紫型先天性心脏病是新生儿中最严重的畸形之一。这种疾病的一种罕见类型是右肺动脉与左心房直接相通,多见于青少年和成年期。然而,考虑到大型分流有可能导致充血性心力衰竭,应尽快予以纠正。
两名患有这种病理性相通的2岁和13岁患者主诉劳力性呼吸困难和中央性发绀。他们的体格检查结果明显,血氧饱和度水平较低。所采用的诊断方法,即心电图、胸部X线、超声心动图、CT扫描以及肺动脉选择性血管造影,显示有异常的右向左血流经右肺动脉和左心房分流。最后,两名患者均通过经导管封堵器成功治疗,无任何并发症,随访期间也无不适主诉。
右肺动脉与左心房先天性异常连接是中央性发绀的罕见原因,大多在青少年期或成年早期出现劳力性呼吸困难和发绀。经胸超声心动图、对比增强CT扫描以及肺动脉血管造影可做出诊断。在过去二十年中,治疗方法已有所发展,从严重病例的手术治疗转变为介入性经皮策略,而对于介入治疗无法实施的病例则仍采用手术治疗。
鉴于未经治疗的右肺动脉与左心房瘘可能危及生命的并发症,如血栓栓塞事件,早期诊断至关重要。然而,治疗这些患者并非总是简单直接,应根据连接瘘的解剖特征、位置、大小和迂曲程度选择治疗策略。尽管血管内治疗是首选方案,但由于某些患者的结构特征,仍需进行手术治疗。