Open Access
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

Authors

  • 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
Further Information

Publication History

30 December 2014

23 January 2015

Publication Date:
04 March 2015 (online)

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.