(Circulation. 1999;99:3086-3087.)
© 1999 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Departments of Pediatrics (P.T.P.) and Diagnostic Radiology (R.Y.S., G.D.R.), Stanford University School of Medicine; the Department of Pediatrics, California-Pacific Medical Center (C.L.A.); the Department of Pediatrics, University of California, San Francisco (P.M.); and The Lucile Salter Packard Children's Hospital.
Correspondence to Paul T. Pitlick, MD, Department of Pediatrics, Stanford University School of Medicine, 750 Welch Rd, Suite 305, Palo Alto, CA 94304.
The patient was a 12-year-old boy who was born with a coarctation of the thoracic aorta. He underwent a Gore-Tex patch angioplasty of the coarctation at 13 days of age. Subsequent restenosis led to subclavian flap angioplasty at age 7 months. He presented now with upper extremity hypertension and decreased femoral pulses.
Attempted visualization of the aortic isthmus by cross-sectional
echocardiography was inadequate. The family was
initially reluctant to consent to a cardiac
catheterization. After 3-dimensional (3D)
reconstruction of electron-beam tomography (EBT) and MRI (Figures 1
and 2
),
the pathological condition was more fully appreciated. The
patient then underwent cardiac catheterization,
angiography (Figure 3
), and balloon
angioplasty of the recurrent coarctation.
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