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隔瓣畸形合并孤立性右旋心:心包部分缺如并肺静脉畸形引流 1 例报告

Malposition of septum primum in isolated dextrocardia: unique and rare form of anomalous pulmonary venous return in association with partial absence of pericardium-case report.

机构信息

Division of Pediatric Cardiac Surgery, Sheikh Khalifa Medical City, PO BOX 51900, Abu Dhabi, United Arab Emirates.

Pediatric Cardiology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.

出版信息

J Cardiothorac Surg. 2021 Jul 31;16(1):211. doi: 10.1186/s13019-021-01591-y.

Abstract

BACKGROUND

Total anomalous pulmonary venous return (TAPVR) refers to an anomaly in which all of the pulmonary veins drain directly or indirectly to the systemic venous circulation. However, unusual types constitute approximately 5% or less of TAPVRs and there may be obstruction or discontinuity of pulmonary vein at various levels.

CASE PRESENTATION

A 3-month-old infant was presented to us with history of poor feeding, respiratory distress and desaturations. The routine echocardiographic investigation initially confirmed the diagnosis of an atrial septal defect with dextrocardia. However, due to disproportionate severity of symptoms and congestive heart failure a cardiac computer tomography angiogram was done that revealed a rare finding of connection of pulmonary veins fused with the posterior atrium, but on the rightward side of the deviated atrial septum. Therefore, pulmonary veins entered a sinus that drains directly into the right atrial superior-posterior wall. During surgical repair, we found an area of absent pericardium in the diaphragmatic surface of the heart. The patient underwent total repair of the TAPVR and patch reconstruction of the pericardial defect. The patient is doing well at 6-month follow up.

CONCLUSIONS

The septum primum malposition defect resulting in TAPVR is a very rare congenital anomaly that can be rarely seen without any heterotaxy. The anomalous features including absent pericardium and dextrocardia were present in this patient have not been described previously with TAPVR. Therefore, we have hypothesized the embryological correlation of absent pericardium and cardiac malposition in such case. Transthoracic echocardiography with Doppler interrogation is a reliable method for diagnosing this condition. In case of suboptimal echocardiographic image due to cardiac position, unclear anatomy or unexplained symptoms, advanced imaging such as computer tomographic angiography or cardiac magnetic resonance imaging can be very helpful. Preoperative proper diagnosis of this anomaly facilitates successful surgical management with excellent outcome.

摘要

背景

完全性肺静脉异位引流(TAPVR)是指所有肺静脉直接或间接引流至体循环的异常。然而,不常见的类型约占 TAPVR 的 5%或更少,并且可能在各级存在肺静脉阻塞或不连续。

病例介绍

一名 3 个月大的婴儿因喂养不良、呼吸窘迫和呼吸暂停就诊。最初的常规超声心动图检查证实了房间隔缺损伴右位心的诊断。然而,由于症状和充血性心力衰竭的严重程度不成比例,进行了心脏计算机断层血管造影检查,发现了一个罕见的发现,即肺静脉与后心房融合,但在偏离的房间隔的右侧。因此,肺静脉进入直接流入右心房后上壁的窦。在手术修复过程中,我们发现心脏膈肌表面有一处心包缺失。患者接受了 TAPVR 的完全修复和心包缺损的补片重建。患者在 6 个月的随访中情况良好。

结论

导致 TAPVR 的隔瓣畸形缺陷是一种非常罕见的先天性异常,在没有任何异位的情况下很少见到。该患者存在异常特征,包括心包缺失和右位心,以前未描述过 TAPVR。因此,我们假设这种情况下心包缺失和心脏位置异常的胚胎学相关性。经胸超声心动图结合多普勒检查是诊断这种情况的可靠方法。如果由于心脏位置、解剖结构不清楚或不明原因的症状导致超声心动图图像不理想,可以使用高级成像,如计算机断层血管造影或心脏磁共振成像,这非常有帮助。术前对这种异常的正确诊断有助于成功的手术管理和良好的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7167/8325803/b5559d3bf908/13019_2021_1591_Fig1_HTML.jpg

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