scholarly journals Interrupted aortic arch: A misdiagnosed cause of hypertension

2014 ◽  
Vol 33 (6) ◽  
pp. 389.e1-389.e5
Author(s):  
Marta Ponte ◽  
Adelaide Dias ◽  
Nuno Dias Ferreira ◽  
Conceição Fonseca ◽  
João Carlos Mota ◽  
...  
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>


Author(s):  
I.V. Novikova, O.M. Khurs, T.V. Demidovich et all

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.


2021 ◽  
Vol 13 (4) ◽  
pp. 309-310
Author(s):  
Maha Tagorti ◽  
Kaouther Hakim ◽  
Hela Msaad ◽  
Khalil Ouaghlani ◽  
Rihab Ben Othmen ◽  
...  

2009 ◽  
Vol 138 (4) ◽  
pp. 924-932 ◽  
Author(s):  
Chloe A. Joynt ◽  
Charlene M.T. Robertson ◽  
Po-Yin Cheung ◽  
Alberto Nettel-Aguirre ◽  
Ari R. Joffe ◽  
...  

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

2003 ◽  
Vol 11 (3) ◽  
pp. 250-254 ◽  
Author(s):  
Kona Samba Murthy ◽  
Robert Coelho ◽  
Christopher Roy ◽  
Snehal Kulkarni ◽  
Benjamin Ninan ◽  
...  

Between 1999 and 2002, 23 patients underwent single-stage complete repair of cardiac anomalies and aortic arch obstruction, without circulatory arrest. Median age was 1.2 years. Intracardiac defects included ventricular septal defect in 9, double-outlet right ventricle in 6, d-transposition of the great arteries and ventricular septal defect in 2, subaortic obstruction in 3, and atrial septal defect in 3. Fourteen patients had coarctation of the aorta, 6 had coarctation with hypoplastic aortic arch, and 3 had interrupted aortic arch. Simple techniques were employed such as cannulation of the ascending aorta near the innominate artery and maintaining cerebral and myocardial perfusion. After correction of arch obstruction, intracardiac repair was undertaken. The mean cardiopulmonary bypass time was 169 min, aortic crossclamp time was 51 min, and arch repair took 16 min. There was no operative mortality or neurological deficit. In follow-up of 1–43 months, no patient had residual coarctation. This simplified technique avoids additional procedures, reduces ischemic time, and prevents problems related to circulatory arrest.


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