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AJP Rep 2015; 05(01): e80-e81
DOI: 10.1055/s-0035-1547331
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta

Shi Zeng
1   Department of Ultrasonography, The Second Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China
,
Qichang Zhou
1   Department of Ultrasonography, The Second Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China
,
Jiawei Zhou
1   Department of Ultrasonography, The Second Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China
,
Qinghai Peng
1   Department of Ultrasonography, The Second Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China
› Author Affiliations
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Publication History

30 December 2014

23 January 2015

Publication Date:
04 March 2015 (online)

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Abstract

The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isolated distal anomalous origin of the right PA from the aorta that was diagnosed by fetal echocardiography at 25 weeks' of gestation. Tracing the course of PA branches is important to make diagnosis.

Keywords

anomalous origin of pulmonary artery from aorta - fetal echocardiography - prenatal diagnosis
 

  • References

  • 1 Garg P, Talwar S, Kothari SS , et al. The anomalous origin of the branch pulmonary artery from the ascending aorta. Interact Cardiovasc Thorac Surg 2012; 15 (1) 86-92
    CrossrefPubMedSearch in Google Scholar
  • 2 Kutsche LM, Van Mierop LH. Anomalous origin of a pulmonary artery from the ascending aorta: associated anomalies and pathogenesis. Am J Cardiol 1988; 61 (10) 850-856
    CrossrefPubMedSearch in Google Scholar
  • 3 Diab K, Richardson R, Pophal S, Alboliras E. Left hemitruncus associated with tetralogy of fallot: fetal diagnosis and postnatal echocardiographic and cardiac computed tomographic confirmation. Pediatr Cardiol 2010; 31 (4) 534-537
    CrossrefPubMedSearch in Google Scholar
  • 4 Oztunç F, Güzeltaş A. Prenatal diagnosis of anomalous origin of the right pulmonary artery from the ascending aorta with hypoplastic right ventricle and pulmonary stenosis. Ultrasound Obstet Gynecol 2008; 32 (4) 592-593
    CrossrefPubMedSearch in Google Scholar
  • 5 Fontana GP, Spach MS, Effmann EL, Sabiston Jr DC. Origin of the right pulmonary artery from the ascending aorta. Ann Surg 1987; 206 (1) 102-113
    CrossrefPubMedSearch in Google Scholar
  • 6 Nathan M, Rimmer D, Piercey G , et al. Early repair of hemitruncus: excellent early and late outcomes. J Thorac Cardiovasc Surg 2007; 133 (5) 1329-1335
    CrossrefPubMedSearch in Google Scholar
  • 7 Jung MJ, Yoo SJ. Prenatal diagnosis of anomalous origin of the right pulmonary artery from the ascending aorta. Cardiol Young 2002; 12 (2) 186-188
    CrossrefPubMedSearch in Google Scholar