Volume 3, Issue 4 pp. 291-294

Giant Cell Aortitis and Noonan Syndrome

Shaji Menon MD

Corresponding Author

Shaji Menon MD

Mayo Congenital Heart Center Mayo Clinic—Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, and

Shaji Menon, MD, Mayo Clinic Pediatric Cardiology, 200 First Street SW, Rochester, MN 55905, USA. Tel: (+1) 507-284-3297; Fax: (+1) 507-284-3968; E-mail: [email protected]Search for more papers by this author
Mary E. Pierpont MD, PhD

Mary E. Pierpont MD, PhD

Childrens Hospital of Minnesota and University of Minnesota—Pediatric Cardiology, Rochester, Minnesota

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David Driscoll MD

David Driscoll MD

Mayo Congenital Heart Center Mayo Clinic—Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, and

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First published: 22 July 2008
Citations: 5

ABSTRACT

An 18-year-old girl with Noonan syndrome was diagnosed with progressive aneurysmal dilatation of the ascending aorta. Histopathological examination revealed giant cell aortitis. Connective tissue abnormalities leading to aortic root dilatation and the sinuses of Valsalva aneurysm have been reported in Noonan syndrome. This report is the first description of giant cell aortitis in Noonan syndrome and may provide a link between aortic aneurysm, and giant cell granuloma of bone in Noonan syndrome.

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