Surgical Management of Right Aortic Arch Obstruction Associated With Rare Form of Vascular Ring

2020 ◽  
Vol 11 (2) ◽  
pp. 222-225
Author(s):  
Evgeny V. Krivoshchekov ◽  
Frank Cetta ◽  
Oleg A. Egunov ◽  
Evgenii A. Sviazov ◽  
Valeriy O. Kiselev ◽  
...  

This clinical case demonstrated surgical management for a rare case of vascular ring associated with an elongated and kinked aortic arch and a right descending aorta in a ten-year-old male using an extra-anatomic bypass grafting method and dividing the vascular ring. Computer tomography performed at six-month follow-up showed a favorable surgical outcome.

2001 ◽  
Vol 71 (2) ◽  
pp. 729-731 ◽  
Author(s):  
Jae Jin Han ◽  
Sejung Sohn ◽  
Hae Soon Kim ◽  
Tae Hee Won ◽  
Jae Ho Ahn

2000 ◽  
Vol 10 (3) ◽  
pp. 212-219 ◽  
Author(s):  
Doff B. McElhinney ◽  
LeNardo D. Thompson ◽  
Paul M. Weinberg ◽  
Kenneth L. Jue ◽  
Frank L. Hanley

AbstractBackgroundAbnormalities of brachiocephalic arterial branching and arch laterality are common in patients with a cervical aortic arch. In addition, structural anomalies of the arch such as obstruction, aneurysms, and tortuosity are found in a significant number of cases.MethodsBetween 1990 and 1998, 6 patients underwent surgery for an obstructed right cervical arch. A significant obstruction was present at the transverse or distal arch in all patients, and was recurrent after previous repair in 2. In 1 patient, there was also a multi-lobed aneurysm of the aortic segment contiguous to the obstruction, and in 2 there was marked tortuosity of the arch. In all cases, the order of origin of the head and neck vessels was abnormal, and obstruction of 1 or more brachiocephalic vessels was found in 3. A vascular ring was present in all patients, with a right aortic arch and aberrant left subclavian artery in 4 patients and a double aortic arch with a dominant right cervical arch in 2. The descending aorta was circumflex (left-sided) in 3 patients. Three patients were repaired through a standard right posterolateral thoracotomy, and 3 through a median sternotomy. Patch augmentation aortoplasty was used in 2 patients, a tube graft from the ascending to descending aorta in 2, end to side anastomosis of the descending aorta to the proximal arch in 1, and direct anastomosis to reconstruct an atretic left-sided component of a double arch in 1.ResultsRepair was successful in all cases, with no perioperative complications. At follow-up ranging from 1 to 9 years, all patients were alive and well, with no recurrence of arch obstruction or other significant complications. Fluorescentin situhybridization revealed microdeletion of chromosome 22q 11 in 1 patient (not performed in the others).ConclusionsStructural anomalies of the arch are relatively common in patients with a cervical aortic arch. Such abnormalities may be the result of hemodynamic conditions and/or abnormal vascular tissue related either to the cervical position of the arch or its embryologic precursors. Given the highly variable anatomy of patients with a complicated cervical aortic arch, surgical considerations will vary in kind.


Circulation ◽  
1981 ◽  
Vol 63 (2) ◽  
pp. 458-460 ◽  
Author(s):  
W Berman ◽  
S M Yabek ◽  
T Dillon ◽  
J F Neal ◽  
B Akl ◽  
...  

Author(s):  
Alexis Palacios-Macedo ◽  
Héctor Díliz-Nava ◽  
Luis García-Benítez ◽  
Fabiola Pérez-Juárez ◽  
Orlando Tamariz-Cruz

We describe the surgical treatment of a patient with hypoplastic left heart syndrome and right aortic arch.


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