A case report of interrupted aortic arch without patent ductus arteriosus and with double‐outlet right ventricle

2019 ◽  
Vol 36 (4) ◽  
pp. 797-799
Author(s):  
Nan Wang ◽  
Feifei Sun ◽  
Weidong Ren ◽  
Wei Qiao ◽  
Xintong Zhang ◽  
...  
2010 ◽  
Vol 58 (5) ◽  
pp. 477
Author(s):  
Hyun-Jeong Kwak ◽  
Hong Soon Kim ◽  
Jong Seok Lee ◽  
Jeongmin Kim ◽  
Joo-Young Chung ◽  
...  

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

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

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.


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