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交叉心脏伴复杂心脏畸形、完全性内脏反位和支气管发育异常。

Criss-cross heart with complex cardiac malformation, situs inversus totalis and bronchial dysplasia.

作者信息

Liang Hongqin, Kong Li, Liu Fei, Ji Xiaojuan, Zhang Nan, Wang Jian

机构信息

Department of Radiology, Third Military Medical University Southwest Hospital (Army Medical University), Chongqing, China.

Department of Ultrasound, Children's Hospital of Chongqing Medical University, Chongqing, China.

出版信息

BMC Cardiovasc Disord. 2025 Apr 2;25(1):248. doi: 10.1186/s12872-025-04659-y.

DOI:10.1186/s12872-025-04659-y
PMID:40175904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11963316/
Abstract

BACKGROUND

Criss-cross heart (CCH) is a rare congenital heart malformation characterized by twisted atrioventricular connections, often associated with various other cardiac anomalies, making accurate diagnosis challenging; In this article, we present a previously unreported case of CCH with complex cardiac malformation, situs inversus totalis, and bronchial dysplasia.

CASE PRESENTATION

A 10-year-old girl presented with recurrent cyanosis and fatigue, and echocardiography revealed a complex congenital heart condition involving CCH, dextrocardia, severe pulmonary hypertension, ventricular septal defect (VSD), atrial septal defect (ASD), and patent ductus arteriosus (PDA). Further CT angiography unveiled bronchial dysplasia and double-outlet right ventricle (DORV).

CONCLUSIONS

CCH is a rare congenital heart condition characterized by twisted atrioventricular connections, with complex associated anomalies. Diagnosis is challenging due to the variety of defects. CT angiography is crucial for comprehensive assessment and surgical planning. This case presented a unique combination of CCH with mirror dextrocardia, situs inversus totalis, and bronchial malformation, highlighting the importance of CT in guiding treatment decisions. However, postoperative follow-up is lacking, and optimal surgical strategies for such complex deformities remain to be explored.

摘要

背景

交叉心脏(CCH)是一种罕见的先天性心脏畸形,其特征为房室连接扭曲,常伴有各种其他心脏异常,这使得准确诊断具有挑战性;在本文中,我们报告了一例此前未报道的伴有复杂心脏畸形、完全性内脏反位和支气管发育不良的CCH病例。

病例介绍

一名10岁女孩出现反复发绀和疲劳,超声心动图显示患有包括CCH、右位心、严重肺动脉高压、室间隔缺损(VSD)、房间隔缺损(ASD)和动脉导管未闭(PDA)的复杂先天性心脏病。进一步的CT血管造影显示支气管发育不良和右心室双出口(DORV)。

结论

CCH是一种罕见的先天性心脏病,其特征为房室连接扭曲,并伴有复杂的相关异常。由于缺陷种类繁多,诊断具有挑战性。CT血管造影对于全面评估和手术规划至关重要。该病例呈现了CCH与镜像右位心、完全性内脏反位和支气管畸形的独特组合,突出了CT在指导治疗决策中的重要性。然而,缺乏术后随访,此类复杂畸形的最佳手术策略仍有待探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/32368dbde78a/12872_2025_4659_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/c20205788190/12872_2025_4659_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/1c4121872325/12872_2025_4659_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/32368dbde78a/12872_2025_4659_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/c20205788190/12872_2025_4659_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/1c4121872325/12872_2025_4659_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37f/11963316/32368dbde78a/12872_2025_4659_Fig3_HTML.jpg

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本文引用的文献

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An electrocardiographic score to predict pulmonary hypertension in children with atrial septal defect.一种用于预测房间隔缺损患儿肺动脉高压的心电图评分。
BMC Pediatr. 2023 Jun 10;23(1):288. doi: 10.1186/s12887-023-04102-1.
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Comparability between Computed Tomography Morphological Vascular Parameters and Echocardiography for the Assessment of Pulmonary Hypertension in Patients with Severe Aortic Valve Stenosis-Results of a Multi-Center Study.计算机断层扫描形态学血管参数与超声心动图在评估重度主动脉瓣狭窄患者肺动脉高压方面的可比性——一项多中心研究结果
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Computed tomography of the airways and lungs in congenital heart disease.
先天性心脏病气道与肺部的计算机断层扫描
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Primary PCI for acute myocardial infarction in a patient with situs inversus totalis and dextrocardia.为一名全内脏反位并右旋心患者的急性心肌梗死进行直接经皮冠状动脉介入治疗。
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Imaging characteristics and associations in twisted atrioventricular connections on multidetector computed tomography angiography.多层螺旋计算机断层血管造影术对扭曲房室连接的成像特征及相关性
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Prenatal Diagnosis and Postnatal Outcome of Eight Cases with Criss-Cross Heart - A Multicenter Case Series.八例十字交叉心的产前诊断及预后:多中心病例系列。
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