scholarly journals Rare case of vascular ring with Kommerell diverticulum mimicking uncontrolled asthma

2020 ◽  
Vol 8 (3) ◽  
Author(s):  
Ahmed Ben Saad ◽  
Nesrine Fahem ◽  
Houda Ben Saad ◽  
Asma Migaou ◽  
Chokri Kortas ◽  
...  
2020 ◽  
Vol 11 (3) ◽  
pp. 377-379
Author(s):  
Truong Ly Thinh Nguyen ◽  
Vinh Quang Tran

Vascular ring malformations usually occur as an isolated lesion. d-Transposition of the great arteries (d-TGA) associated with vascular ring malformations has seldom been reported in the literature. In this report, we describe two unusual cases of d-TGA associated with non-Kommerell diverticulum resulting in vascular ring. Our approach for the diagnosis and surgical management of this unusual combination of congenital heart lesions is described.


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.


2014 ◽  
Vol 24 (4) ◽  
pp. 727-728
Author(s):  
Deepa Prasad ◽  
Manish Bansal ◽  
Ravi C. Ashwath

AbstractWe describe a rare case of double vascular ring diagnosed with cardiac magnetic resonance imaging in a patient with ventricular septal defect, pulmonary stenosis, and right aortic arch.


2017 ◽  
Vol 44 (2) ◽  
pp. 138-140
Author(s):  
Jonathan B. Wagner ◽  
Joshua Q. Knowlton ◽  
Peter Pastuszko ◽  
Sanket S. Shah

A male neonate presented with CHARGE syndrome, a multiorgan genetic disorder involving the Coloboma of the eyes, congenital Heart defects, nasal choanal Atresia, growth and development Retardation, Genitourinary disorders, and Ear anomalies and deafness. Moreover, he had a rare case of vascular ring—consisting of a right aortic arch with retroesophageal brachiocephalic artery—combined with coarctation of the mid-aortic arch. He underwent both vascular ring and aortic arch repair at our institution. To our knowledge, this is the 4th documented case of this exceedingly rare type of aortic arch anomaly combined with aortic arch obstruction. Moreover, it is the first confirmed case of these combined disorders occurring in CHARGE syndrome. This report describes a truly rare case and reveals the limitations of echocardiography in detecting complex aortic arch anomalies while illustrating the benefits of advanced imaging prior to surgical intervention.


Author(s):  
Nabil Dib ◽  
Thibaut Lapotre ◽  
Jacques Tomasi ◽  
Nabila El Gueddari ◽  
Amedeo Anselmi ◽  
...  

2015 ◽  
Vol 100 (6) ◽  
pp. 2293-2297 ◽  
Author(s):  
Deborah Luciano ◽  
Julia Mitchell ◽  
Alain Fraisse ◽  
Hubert Lepidi ◽  
Bernard Kreitmann ◽  
...  

2020 ◽  
Vol 104 (1-2) ◽  
pp. 39-42
Author(s):  
Raymond A. Dieter ◽  
George B. Kuzycz ◽  
Robert W. Kemp ◽  
Juliet H. Fallah ◽  
Deborah M. Budris ◽  
...  

A 24 year-old Hispanic man presented with progressive retrosternal chest pain, shortness of breath, and dysphagia. Chest X-ray, computed tomography angiography, and magnetic resonance (MRA) studies were compatible with a right aortic arch and a 3.5-cm descending right aortic Kommerell diverticulum. Barium esophagogram and esophagoscopy demonstrated a constricting band crossing the esophagus at the level of the diverticulum. After discussion with other cardiothoracic surgeons, with a combined 300 years of experience, they reported only 1 other possible such case. Kommerell's diverticula are usually repaired in children and rarely are seen in the adult. Kommerell diverticular treatment options include endovascular stenting, cardiopulmonary bypass with resection and grafting, right thoracotomy, and a cervical approach. Because of the patient's findings of a right arch, a Kommerell diverticulum, and a constricting band causing esophageal compression and respiratory distress, it was felt stenting alone would not relieve his symptoms. Therefore, we used a left third posterior intercostal thoracotomy approach to resect the constricting esophageal band connecting the Kommerell diverticulum to the left subclavian artery and to perform the Kommerell diverticulectomy. Releasing the esophageal and tracheal compressing band and resection of the diverticulum provided complete symptom relief with elimination of the dysphagia, dyspnea, wheezing, and chest pain, using a single surgical procedure.


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