Idiopathic midaortic syndrome

David Saul; Rahul Nikam; Vinay Kandula; Achala Donuru

doi:10.4103/apc.apc_261_20

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Idiopathic midaortic syndrome

David Saul¹, Rahul Nikam¹, Vinay Kandula¹, Achala Donuru²
¹ Department of Medical Imaging, Nemours Alfred I. DuPont Hospital for Children, Wilmington, DE 19803, USA
² Department of Radiology, Thomas Jefferson University Hospitals, Philadelphia, PA 19107, USA

Correspondence Address:
Dr. Achala Donuru
Department of Radiology, Thomas Jefferson University Hospitals, 132 S 10^th Street, 1079 Main Building, Philadelphia, PA 19107
USA

Source of Support: None, Conflict of Interest: None

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DOI: 10.4103/apc.apc_261_20

Year : 2021 | Volume : 14 | Issue : 4 | Page : 561-563

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Midaortic syndrome (MAS) is characterized by narrowing of the descending aorta between the distal aortic arch and the aortic bifurcation. We present the case of a 4-year-old male presenting with a murmur and diagnosed with MAS. He was treated with a thoracoabdominal bypass graft.

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Correspondence Address:
Dr. Achala Donuru
Department of Radiology, Thomas Jefferson University Hospitals, 132 S 10^th Street, 1079 Main Building, Philadelphia, PA 19107
USA

Source of Support: None, Conflict of Interest: None

Check

DOI: 10.4103/apc.apc_261_20