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2
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引用本文的文献

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Antenatal Diagnosis of Double Aortic Arch.双主动脉弓的产前诊断
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本文引用的文献

1
Late diagnosis of double aortic arch: consequences on long-term follow-up.双主动脉弓的延迟诊断:长期随访结果
Pediatr Pulmonol. 2014 Mar;49(3):E75-7. doi: 10.1002/ppul.22852. Epub 2013 Jul 16.
2
Anomalies of the derivatives of the aortic arch system.主动脉弓系统衍生物的异常。
Med Clin North Am. 1948 Jul;32:925-49. doi: 10.1016/s0025-7125(16)35662-0.
3
Etiology of stridor in infants.婴儿喘鸣的病因
Ann Otol Rhinol Laryngol. 2007 May;116(5):329-34. doi: 10.1177/000348940711600503.
4
Management and outcomes of double aortic arch in 81 patients.81例双主动脉弓患者的管理及预后
Pediatrics. 2006 Nov;118(5):e1336-41. doi: 10.1542/peds.2006-1097. Epub 2006 Sep 25.
5
Trends in vascular ring surgery.血管环手术的发展趋势
J Thorac Cardiovasc Surg. 2005 Jun;129(6):1339-47. doi: 10.1016/j.jtcvs.2004.10.044.
6
Imaging findings in pediatric patients with persistent airway symptoms after surgery for double aortic arch.双主动脉弓手术后出现持续性气道症状的儿科患者的影像学表现
AJR Am J Roentgenol. 2002 May;178(5):1275-9. doi: 10.2214/ajr.178.5.1781275.
7
Sonographic diagnosis of fetal vascular rings in early pregnancy.孕早期胎儿血管环的超声诊断
Am J Cardiol. 1998 Jan 1;81(1):101-3. doi: 10.1016/s0002-9149(97)00864-3.
8
Surgical treatment of vascular rings: the Mayo Clinic experience.血管环的外科治疗:梅奥诊所的经验
Mayo Clin Proc. 1993 Nov;68(11):1056-63. doi: 10.1016/s0025-6196(12)60898-2.
9
Airway obstruction in aortic arch anomalies.主动脉弓畸形中的气道梗阻
Otolaryngol Head Neck Surg. 1983 Dec;91(6):605-9. doi: 10.1177/019459988309100603.

胎儿双主动脉弓的产前诊断:一例报告。

Prenatal diagnosis of fetal double aortic arch: report of a case.

作者信息

Gou Zhongshan, He Yihua, Zhang Ye, Gu Xiaoyan

机构信息

Department of Echocardiography, Beijing Anzhen Hospital, Capital Medical University Beijing, China.

出版信息

Int J Clin Exp Pathol. 2015 Oct 1;8(10):13565-7. eCollection 2015.

PMID:26722575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4680520/
Abstract

Double aortic arch (DAA) is the most common congenital anomaly of the aortic arch system, in which the trachea and esophagus are completely encircled by connected segments of the aortic arch and its branches, often resulting in variable airway compression. We present a case of fetal DAA prenatally diagnosed by fetal echocardiography and clearly confirmed at autopsy. The autopsy visualization allowed for better understanding of this rare cardiac anomaly and facilitated improving the prenatal diagnostic rate.

摘要

双主动脉弓(DAA)是主动脉弓系统最常见的先天性异常,其中气管和食管被主动脉弓及其分支的相连节段完全环绕,常导致不同程度的气道受压。我们报告一例通过胎儿超声心动图产前诊断并经尸检明确证实的胎儿双主动脉弓病例。尸检所见有助于更好地理解这种罕见的心脏异常,并有助于提高产前诊断率。