RARE CASE OF DOUBLE AORTIC-ARCH WITH HYPOPLASTIC RIGHT DORSAL SEGMENTAND ASSOCIATED TETRALOGY OF FALLOT - MR FINDINGS

Citation
La. Kramer et al., RARE CASE OF DOUBLE AORTIC-ARCH WITH HYPOPLASTIC RIGHT DORSAL SEGMENTAND ASSOCIATED TETRALOGY OF FALLOT - MR FINDINGS, Magnetic resonance imaging, 11(8), 1993, pp. 1217-1221
Citations number
NO
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
Journal title
ISSN journal
0730725X
Volume
11
Issue
8
Year of publication
1993
Pages
1217 - 1221
Database
ISI
SICI code
0730-725X(1993)11:8<1217:RCODAW>2.0.ZU;2-K
Abstract
We report a rare case of double aortic arch with a hypoplastic right d orsal arch segment, which was also associated with tetralogy of Fallot . Accurate characterization of the hypoplastic right arch segment by M RI preoperatively determined the optimal surgical approach to releasin g the symptomatic vascular ring. MRI was also useful in assessing and monitoring associated tracheomalacia.