A rare association of interrupted aortic arch type C and microdeletion 22q11.2

2007 ◽  
Vol 167 (10) ◽  
pp. 1195-1198 ◽  
Author(s):  
Goran Cuturilo ◽  
Danijela Drakulic ◽  
Milena Stevanovic ◽  
Ida Jovanovic ◽  
Milan Djukic ◽  
...  
Keyword(s):  
Aortic Arch ◽  
Interrupted Aortic Arch ◽  
Rare Association ◽  
Type C ◽  
Microdeletion 22Q11.2

Isolated Type C Interrupted Aortic Arch in Adult: Extra-anatomic Repair Using Circulatory Arrest

2013 ◽  
Vol 28 (4) ◽  
pp. 239-241
Author(s):  
Xing-rong Liu ◽  
Qi Miao ◽  
Guo-tao Ma ◽  
Chao-ji Zhang ◽  
Li-hua Cao
Keyword(s):  
Aortic Arch ◽  
Circulatory Arrest ◽  
Interrupted Aortic Arch ◽  
Anatomic Repair ◽  
Type C

Biventricular Repair in Interrupted Aortic Arch Type C With Aortic Atresia

2017 ◽  
Vol 10 (2) ◽  
pp. 228-230 ◽  
Author(s):  
Dhananjay P. Malankar ◽  
Andrew C. Glatz ◽  
Paul M. Weinberg ◽  
James W. Gaynor
Keyword(s):  
Ventricular Septal Defect ◽  
Aortic Arch ◽  
Septal Defect ◽  
Interrupted Aortic Arch ◽  
Single Stage ◽  
Initial Operation ◽  
Biventricular Repair ◽  
Aortic Atresia ◽  
Type C ◽  
Arch Reconstruction

We report a case of interrupted aortic arch type C with aortic atresia and a ventricular septal defect with two well-developed ventricles, who underwent a successful single-stage biventricular repair with the modified Yasui procedure and arch reconstruction. Angiography done during conduit revision showed bilateral brachiocephalic trunks with high branching. The child is doing well six years after the initial operation.

scholarly journals Aortic atresia, interrupted aortic arch type C perfused by bilateral arterial duct

2005 ◽  
Vol 26 (21) ◽  
pp. 2333-2333 ◽  
Author(s):  
Wim Decaluwe ◽  
Tammo Delhaas ◽  
Marc Gewillig
Keyword(s):  
Aortic Arch ◽  
Interrupted Aortic Arch ◽  
Arterial Duct ◽  
Aortic Atresia ◽  
Type C

Type B Interrupted Aorta in an Adult Patient

2014 ◽  
Vol 17 (2) ◽  
pp. 80
Author(s):  
Ahmet Ozkara ◽  
Mehmet Ezelsoy ◽  
Levent Onat ◽  
Ilhan Sanisoglu
Keyword(s):  
Cardiopulmonary Bypass ◽  
Aortic Arch ◽  
Collateral Circulation ◽  
Neonatal Period ◽  
Interrupted Aortic Arch ◽  
Complete Loss ◽  
Posterolateral Thoracotomy ◽  
Type B ◽  
Case Presentation ◽  
Descending Aorta

<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>

Conotruncal heart defects and aortic arch anomalies in fetuses with 22q11.2 deletion syndrome

2020 ◽  
Author(s):  
I.V. Novikova, O.M. Khurs, T.V. Demidovich et all
Keyword(s):  
Aortic Arch ◽  
Heart Defects ◽  
22Q11.2 Deletion Syndrome ◽  
Ventricular Outflow Tract ◽  
Double Outlet Right Ventricle ◽  
Interrupted Aortic Arch ◽  
Left Ventricular ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion ◽  
Aortic Arch Anomalies

16 second trimester fetuses with 22q11.2 deletion syndrome have been examined at anatomic-pathological investigation. Main cardiovascular diseases were ascending aorta hypoplasia with aortic valve stenosis (n = 6; 37.5%), truncus arteriosus (n = 5; 31.25%), tetralogy of Fallot (n = 3; 18.75%) and double-outlet right ventricle (n = 1; 6.25%). Ventricular septal defect was present in 16 cases. Associated aortic arch anomalies included interrupted aortic arch (n = 9; 56.25%), right aortic arch (n = 6; 37.5%), retroesophageal ring (n = 1; 6.25%) and aberrant right subclavian arteria (n = 5; 31.25%). 5 fetuses had left ventricular outflow tract obstructive lesions with interrupted aortic arch of type B combined with aberrant right subclavian arteria.

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