Middle Aortic Syndrome Repair in a 14-Month-Old Child: A 24-Year Case Study.

World J Pediatr Congenit Heart SurgApr 8, 2026 (epub)

Mauricio Gonzalez-Urquijo, Francisco Valdes, Jose Francisco Vargas et al.

✦ AI-curated · Sources linked

Case in brief

A 14-month-old boy with severe hypertension and recurrent heart failure was found to have juxta-diaphragmatic aortic coarctation from mid-aortic syndrome. An 8 mm polytetrafluoroethylene thoracoabdominal aorto-aortic bypass resolved his symptoms. At age 14, exercise-induced claudication developed as he outgrew the graft; recanalization of the native aorta with a covered stent restored distal perfusion, and subsequent stent compression was treated with a bare metal stent. At age 24, he was asymptomatic, normotensive, and physically active, with normal ankle-brachial indices and distal perfusion despite occlusion of the original bypass.

What made this case unusual

The long-term course illustrates how growth-related graft limitation and later stent compression were managed by restoring flow through the native aorta, which remained widely patent at age 24 despite occlusion of the original bypass.

Diagnostic / clinical pearl

In a young child with severe hypertension and recurrent heart failure, consider mid-aortic syndrome; after repair, long-term surveillance can identify growth-related graft limitation and endovascular complications.

Source

Published in World J Pediatr Congenit Heart Surg. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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