Prenatal diagnosis of aortic arch anomalies: Echocardiography, 3D ‐ultrasonography, and computed tomography angiogram findings. A case‐report

Author(s):  
Nathalie Jeanne Bravo‐Valenzuela ◽  
Marcelo Souto Nacif ◽  
Edward Araujo Júnior
2013 ◽  
Vol 45 (2) ◽  
pp. 182-185 ◽  
Author(s):  
Kerry L. Ahrens ◽  
Scott B. Reeder ◽  
Jon G. Keevil ◽  
Janis P. Tupesis

Author(s):  
Nura Fitnat Topbas Selcuki ◽  
Gokalp Senol ◽  
Didem Esin ◽  
Zeynep Gedik Ozkose ◽  
Sema Suzen Caypinar ◽  
...  

2021 ◽  
Vol 24 (2) ◽  
pp. E407-E408
Author(s):  
Xin Wang ◽  
Bofu Liu ◽  
Haifang Yu

Aortic dissection (AD) is a life-threatening disease, and endovascular repair by stent graft is an effective treatment. Surgery often fails for a variety of reasons, such as aortic arch variation. We present the case of a 27-year-old female with aortic dissection with a rare anatomical aortic arch variation caused by chest trauma. This patient recovered well after endovascular repair. This case report demonstrates endovascular repair can be applied to aortic dissection patients with rare anatomical aortic arch variation.


2018 ◽  
Vol 8 (1) ◽  
pp. 64-70
Author(s):  
Julia Murlewska ◽  
Agnieszka Żalińska ◽  
Danuta Roik ◽  
Bożena Werner ◽  
Maria Respondek-Liberska

Abstract This case report presents a prenatal diagnosis with postnatal confirmation (by angio CT and computer reconstruction) of an isolated double aortic arch, with no blood disturbances and with no clinical symptoms after birth. Literature review was focusing on the possible symptoms in the future. Prenatal findings should be forwarded to neonatologist and pediatrician despite clinical silence.


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