2022
DOI: 10.1016/j.radcr.2022.07.084
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Complete interruption of aortic arch diagnosed in adulthood: a case report

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Cited by 3 publications
(3 citation statements)
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“…The prevalence of interrupted descending aorta (IDA) is approximately 1% of all congenital heart diseases, affecting three per million live births, making it an extremely rare anomaly, and its confluence with other structural anomalies like severe aortic stenosis (AS) and bicuspid aortic valve (BAV) makes it a rare clinical scenario, making it a complex cardiovascular conundrum, as presented in our case. While most cases are diagnosed in infancy or early childhood, very few adult-onset cases have been reported [ 1 ]. In this complex scenario, multiple congenital anomalies converge to create a challenging clinical condition.…”
Section: Introductionmentioning
confidence: 99%
“…The prevalence of interrupted descending aorta (IDA) is approximately 1% of all congenital heart diseases, affecting three per million live births, making it an extremely rare anomaly, and its confluence with other structural anomalies like severe aortic stenosis (AS) and bicuspid aortic valve (BAV) makes it a rare clinical scenario, making it a complex cardiovascular conundrum, as presented in our case. While most cases are diagnosed in infancy or early childhood, very few adult-onset cases have been reported [ 1 ]. In this complex scenario, multiple congenital anomalies converge to create a challenging clinical condition.…”
Section: Introductionmentioning
confidence: 99%
“…This disorder is more common and ca uses 5%-8% of congenital cardiac abnormalities [5].Conversely, IAA denotes a congenital aortic arch deformity wherein the ascendin g and descending aortas do not have a direct physical relationshi p. Unlike CoA, IAA is a real discontinuity phenomeon [6][7][8]. CoA a nd IAA are correlated despite their being two distinct conditions [6].Congenital conditions or total blockage following CoA can resul t in adult aortic arch interruption, particularly in patients with ext ensive lesion regions and protracted disease [9]. Patients with both illnesses need a large amount of collateral circulation to survive, and whether or not enough collateral circulation forms to sustai n distal blood flow determines whether or not a patient may live to adulthood [9].…”
mentioning
confidence: 99%
“…CoA a nd IAA are correlated despite their being two distinct conditions [6].Congenital conditions or total blockage following CoA can resul t in adult aortic arch interruption, particularly in patients with ext ensive lesion regions and protracted disease [9]. Patients with both illnesses need a large amount of collateral circulation to survive, and whether or not enough collateral circulation forms to sustai n distal blood flow determines whether or not a patient may live to adulthood [9]. Most IAA cases are discovered and treated in i nfancy or during the neonatal period, as this stage has a faster r ate of child development, a smaller load on the heart, and bette r surgical treatment outcomes.…”
mentioning
confidence: 99%