scholarly journals Short-Segment Type B Interrupted Aortic Arch Presenting With Subarachnoid Hemorrhage With Subsequent Primary Percutaneous Repair

2021 ◽  
Vol 3 (14) ◽  
pp. 1607-1609
Author(s):  
Abhinay Ramachandran ◽  
Michael Argilla ◽  
Sunil Saharan ◽  
Dan Halpern ◽  
Adam Small
2014 ◽  
Vol 17 (2) ◽  
pp. 80
Author(s):  
Ahmet Ozkara ◽  
Mehmet Ezelsoy ◽  
Levent Onat ◽  
Ilhan Sanisoglu

<p><b>Introduction:</b> Interrupted aortic arch is a rare congenital malformation characterized by a complete loss of luminal continuity between the ascending and descending aorta. It is often diagnosed during the neonatal period.</p><p><b>Case presentation:</b> We presented a 51-year-old male patient with interrupted aortic arch type B who was treated successfully with posterolateral thoracotomy without using cardiopulmonary bypass.</p><p><b>Conclusion:</b> The prognosis for interrupted aortic arch depends on the associated congenital anomalies, but the outcome is usually very poor unless there is surgical treatment. Survival into adulthood depends on the development of collateral circulation.</p>


2014 ◽  
Vol 38 (1) ◽  
pp. 60-62 ◽  
Author(s):  
Suat Eren ◽  
Mecit Kantarci ◽  
Berhan Pirimoglu ◽  
Murteza Cakir ◽  
Hayri Ogul

1994 ◽  
Vol 24 (3) ◽  
pp. 523
Author(s):  
Seung Ho Park ◽  
Hyuck Moon Kwon ◽  
June Kwan ◽  
Joon Han Shin ◽  
Myeong Ki Hong ◽  
...  

1994 ◽  
Vol 9 (1) ◽  
pp. 44-52 ◽  
Author(s):  
Kazuo Momma ◽  
Masahiko Ando

2020 ◽  
Vol 30 (11) ◽  
pp. 1732-1734
Author(s):  
Muhammed Riyas K. Rahmath ◽  
Younes Boudjemline ◽  
Reema Y. Kamal

AbstractA combination of aortic valve atresia and an interrupted aortic arch is a unique disease in which perfusion to the brain and myocardium depends on coexisting lesions or type of interruption. We report a case of aortic valve atresia with type B interrupted arch, bilateral arterial ductus in a neonate who was successfully palliated using a hybrid approach by placing stents in both arterial ductus and banding of branch pulmonary arteries.


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