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Ann Thorac Surg 2001;71:2043-2044
© 2001 The Society of Thoracic Surgeons

Case report

Anomalous origin of innominate artery from right pulmonary artery in DiGeorge syndrome

Kagami Miyaji, MDa, Robert L. Hannan, MDa, Redmond P. Burke, MDa

a Department of Cardiovascular Surgery and Cardiology, Miami Children’s Hospital, Miami, Florida, USA

Accepted for publication May 1, 2000.

Address reprint requests to Dr Burke, Department of Cardiovascular Surgery and Cardiology, Miami Children’s Hospital, 3200 SW 60 Court, Suite 102, Miami, FL 33155
e-mail: redmond111{at}aol.com

We experienced a case of anomalous origin of innominate artery from right pulmonary artery (isolated innominate artery). This patient was a 2-month-old baby girl weighing 3.2 kg with DiGeorge syndrome, who was diagnosed with perimembranous ventricular septal defect, atrial septal defect, and patent ductus arteriosus. This type of anomaly is exceedingly rare.






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