scholarly journals Type B Interrupted Aortic Arch with a Patent Ductus Arteriosus in an Adult Presenting with Secondary Polycythaemia

Author(s):  
Jonan Chun Yin Lee ◽  
Jeanie Betsy Chiang ◽  
Boris Chun Kei Chow

Interrupted aortic arch (IAA) is an extremely rare congenital cyanotic heart disease characterized by complete disruption between the ascending and descending aorta. A patent ductus arteriosus (PDA) or other collateral pathways provide blood flow to the distal descending aorta. Mortality is extremely high at early infancy, particularly after the closure of ductus arteriosus. Survival and presentation in adulthood are extremely rare. Here we illustrate a rare case of type B interrupted aortic arch in an adult who presented with secondary polycythaemia. The blood supply to descending aorta and beyond is almost solely by a patent ductus arteriosus. The case demonstrates the value of multimodality imaging including CT and MRI for diagnosis and treatment planning in these patients.

2019 ◽  
Vol 52 ◽  
pp. 50-54
Author(s):  
Jeremy R. Burt ◽  
Vincent Grekoski ◽  
Fiona Tissavirasingham ◽  
Ryan Parente ◽  
Jorge Garcia

1977 ◽  
Vol 74 (6) ◽  
pp. 913-917 ◽  
Author(s):  
Kenji Ito ◽  
Naoaki Kohguchi ◽  
Yasunori Ohkawa ◽  
Tadayoshi Akasaka ◽  
Hiroshi Ohara ◽  
...  

Circulation ◽  
2015 ◽  
Vol 131 (15) ◽  
Author(s):  
Hoang H. Nguyen ◽  
Elizabeth Sheybani ◽  
Peter Manning ◽  
Tom Herman ◽  
Shafkat Anwar

2010 ◽  
Vol 58 (5) ◽  
pp. 477
Author(s):  
Hyun-Jeong Kwak ◽  
Hong Soon Kim ◽  
Jong Seok Lee ◽  
Jeongmin Kim ◽  
Joo-Young Chung ◽  
...  

PEDIATRICS ◽  
1950 ◽  
Vol 5 (3) ◽  
pp. 390-395
Author(s):  
FORREST H. ADAMS ◽  
JOHN LABREE ◽  
HERBERT M. STAUFFER

Two patients with atypical findings of a patent ductus arteriosus are presented in whom right heart catheterization proved its existence by the catheter passing through the ductus into the aorta. Right heart catheterization in one of these patients demonstrated a right descending aorta in the presence of a left aortic arch, the fourth patient with this anomaly to be reported.


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