An adult with central cyanosis and differential pulmonary vascularity

Rajiv Ananthakrishna, Nagaraja Moorthy, Dattatreya P.V. Rao, Manjunath C. Nanjappa

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

A 22-year-old male patient presented with progressive effort intolerance of 2-years duration. Clinical findings and investigations were suggestive of Tetralogy of Fallot (TOF). In addition, there was a conspicuous difference in the pulmonary vascularity with oligemia on the left side and relative hypervascularity on the right side. The right pulmonary artery was arising from the proximal ascending aorta and the main pulmonary artery was continuing as the left pulmonary artery. The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is a rare cardiac anomaly. We report this condition in association with TOF, highlighting the differential pulmonary vascularity.

LanguageEnglish
Pages253-254
Number of pages2
JournalAnnals of Pediatric Cardiology
Volume8
Issue number3
DOIs
Publication statusPublished - 12 Nov 2015

Keywords

  • Anomalous origin
  • congenital heart disease
  • pulmonary artery
  • pulmonary vascularity

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Cardiology and Cardiovascular Medicine

Cite this

Ananthakrishna, R., Moorthy, N., Rao, D. P. V., & Nanjappa, M. C. (2015). An adult with central cyanosis and differential pulmonary vascularity. Annals of Pediatric Cardiology, 8(3), 253-254. https://doi.org/10.4103/0974-2069.150701