Rare arch and supra-aortic vessel anomaly
نویسندگان
چکیده
منابع مشابه
Rare arch and supra-aortic vessel anomaly.
Cortez G, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2017-220718 Description A 3-year-old child with history of a large secundum atrial septal defect came to our institution for surgical cardiovascular evaluation. The patient had reached all developmental milestones and was completely asymptomatic. During imaging workup, a three-dimensional magnetic resonance angiography (MRA) reconstruction sho...
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Interrupted aortic arch (IAA) is a rare congenital cardiac defect defined as complete loss of luminal and anatomical continuity between the ascending and descending segments of the aorta. Very few patients can reach adult age without surgical correction. These cases showed diagnosis of the nearly asymptomatic Type A IAA with aortography and multislice computed tomography (MSCT). A 27year-old ma...
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Here, we report a fetus with a rare aortic arch anomaly with left aortic arch and right ductus arteriosus, which has not been reported so far. In this condition, the aorta extends to the left of the trachea as in normal, while the ductus arteriosus extends to the right of the trachea and joins the descending aorta posterior to the trachea, with a cross-ribbon sign.
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Background Vascular ring is less than 1% of congenital heart disease. Double aortic arch (DAA) is the most common form of it. Its detecting is important because of the effects of pressure on the esophagus and trachea. Case Report In this study, three children suffering from double aortic arch with symptoms of dysphagia and recurrent aspiration, which in two cases had led to cardiac arrest, wer...
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Angiography in a 30-year-old man revealed the unique combination of aortic coarctation and an unusual arch anomaly. Proximal to the coarctation, a single arch vessel trifurcated into the brachiocephalic, left common carotid and left subclavian arteries. This anomalous arch vessel is a normal equine variant.
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2017
ISSN: 1757-790X
DOI: 10.1136/bcr-2017-220718