2015
DOI: 10.1016/j.radcr.2015.06.001
|View full text |Cite
|
Sign up to set email alerts
|

Interrupted aortic arch with post-interruption aneurysm and bicuspid aortic valve in an adult: a case report and literature review

Abstract: Interrupted aortic arch in adults is rare with a limited number of reported cases. We describe a case of a 53-year-old woman with interrupted aortic arch, bicuspid aortic valve, and post-interruption saccular aneurysm of the aorta. To our knowledge, this is only the second report of an adult patient with all 3 abnormalities. We also review the literature on this unusual condition and discuss its relationship with coarctation of the aorta.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
27
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 26 publications
(27 citation statements)
references
References 9 publications
0
27
0
Order By: Relevance
“…IAA may be associated with other congenital heart diseases like ventricular septal defect, PDA and bicuspid aortic valve. Type B is also associated with subaortic stenosis due to malalignment of outlet conal septum (71). IAA is generally seen in patients with 22q11 deletion syndrome, predominantly involving type B (69).…”
Section: Iaamentioning
confidence: 99%
“…IAA may be associated with other congenital heart diseases like ventricular septal defect, PDA and bicuspid aortic valve. Type B is also associated with subaortic stenosis due to malalignment of outlet conal septum (71). IAA is generally seen in patients with 22q11 deletion syndrome, predominantly involving type B (69).…”
Section: Iaamentioning
confidence: 99%
“…Interrupted aortic arch (IAA) is defined as a complete loss of luminal and anatomic continuity between ascending and descending parts of the aorta 1 . IAA is an uncommon congenital malformation of the aortic arch that occurs in 3 per million live births and accounts for only 1% of all congenital heart disease 1 . IAA is much more frequently encountered in the neonate, and immediate surgical intervention remains the only therapy.…”
Section: Introductionmentioning
confidence: 99%
“…As for IAA in adult patient, it is extremely uncommon with only 40 cases documented so far. Of the 40 reported adult patients with IAA, only 3 presented with congestive heart failure as IAA in the adult usually develops extensive collateral arteries 14 . IAA in adult patients can live for many years asymptomatically due to existence of extensive collateral arteries (CAs), and whether these patients should be treated medically or with surgical repair has not been determined.…”
Section: Introductionmentioning
confidence: 99%
“…[6] In neonates, 53% of the cases are type B, followed by types A (43%) and C (4%). [7] However, the presentation of IAA in adulthood was obviously different. In a review of 38 cases of IAA in adulthood, 79% of these patients were type A, followed by types B and C with 16% and 3%, respectively.…”
Section: Discussionmentioning
confidence: 99%