This report describes the unique case of a completely patent Double Aortic Arch (DAA) combined with Kommerell Diverticulum (KD), absence of celiac trunk and congenital asplenia. The anatomical variants described were identified and assessed in a 51-year old female from a computed-tomography angiography (CTA) images with 3D-volume rendered reconstructions during her follow-up after hysterectomy. The reconstructed CTA images showed a DAA with the left common carotid artery stemming from the hypoplastic left aortic arch while the left subclavian artery originated from a KD in the descending thoracic aorta. A symmetric arrangement of the aortic arch branches was demonstrated, comprising a full vascular ring. Since the patient had been complete...
Background: Kommerell's diverticulum is a rare vascular anomaly characterized as an outpouch at the ...
Congenital abnormalities of the aortic arch stem from a defect in the unilateral disappearance of ar...
IntroductionWe report a case of Kommerell's diverticulum of an aberrant right subclavian artery in a...
A 52-year-old male with a history of aortic ectasia was referred to a computed tomography (CT) scan ...
A 52-year-old male with a history of aortic ectasia was referred to a computed tomography (CT) scan ...
Kommerell's diverticulum is a rare congenital disorder characterized by typical right sided aortic a...
Thoracic aortic anomalies are rare and may be associated with pathologic vascular conditions necessi...
We present a rare case of isolated right subclavian artery arising from a right-sided patent arteria...
A right-sided aortic arch is a rare congenital defect of the aorta. It is seen in approximately 0.1...
Introduction: A right-sided aortic arch is a rare congenital cardiovascular anomaly that arises from...
A 31-year-old woman presented with blood pressuresomewhat lower on the left compared with the right ...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
We recently read the interesting article by Albayram et al (1), which concisely explained the anomal...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
Background: Kommerell's diverticulum is a rare vascular anomaly characterized as an outpouch at the ...
Congenital abnormalities of the aortic arch stem from a defect in the unilateral disappearance of ar...
IntroductionWe report a case of Kommerell's diverticulum of an aberrant right subclavian artery in a...
A 52-year-old male with a history of aortic ectasia was referred to a computed tomography (CT) scan ...
A 52-year-old male with a history of aortic ectasia was referred to a computed tomography (CT) scan ...
Kommerell's diverticulum is a rare congenital disorder characterized by typical right sided aortic a...
Thoracic aortic anomalies are rare and may be associated with pathologic vascular conditions necessi...
We present a rare case of isolated right subclavian artery arising from a right-sided patent arteria...
A right-sided aortic arch is a rare congenital defect of the aorta. It is seen in approximately 0.1...
Introduction: A right-sided aortic arch is a rare congenital cardiovascular anomaly that arises from...
A 31-year-old woman presented with blood pressuresomewhat lower on the left compared with the right ...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
We recently read the interesting article by Albayram et al (1), which concisely explained the anomal...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
In early embryogenesis, aortic anomalies occur as a consequence of disorders in the development of t...
Background: Kommerell's diverticulum is a rare vascular anomaly characterized as an outpouch at the ...
Congenital abnormalities of the aortic arch stem from a defect in the unilateral disappearance of ar...
IntroductionWe report a case of Kommerell's diverticulum of an aberrant right subclavian artery in a...