Hostname: page-component-745bb68f8f-grxwn Total loading time: 0 Render date: 2025-01-22T11:05:26.727Z Has data issue: false hasContentIssue false
  • English
  • Français

Severe coronary artery ectesia in a paediatric patient with Noonan syndrome presenting for transcatheter pulmonary valve placement

Published online by Cambridge University Press:  13 January 2025

Christopher Herron Open the ORCID record for Christopher Herron [Opens in a new window] ,
Karen Iacono  and
David Nykanen
Christopher Herron*
Affiliation:
Department of Pediatric Cardiology, Arnold Palmer Hospital for Children, Orlando, FL, USA
Karen Iacono
Affiliation:
Department of Pediatric Cardiology, Arnold Palmer Hospital for Children, Orlando, FL, USA
David Nykanen
Affiliation:
Department of Pediatric Cardiology, Arnold Palmer Hospital for Children, Orlando, FL, USA
*
Corresponding author: Christopher Herron; Email: christopher.herron@orlandohealth.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Coronary ectasia is a very rare phenomenon seen in Noonan syndrome with only a few documented case reports. We describe a 14-year-old with Noonan syndrome and tetralogy of Fallot with described coronary artery ectasia since infancy who presented for possible transcatheter pulmonary valve placement and was found to have severe ectasia of bilateral coronary arteries.

Keywords

Noonan syndromecoronary dilationpulmonary stenosis
Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , First View , pp. 1 - 3
Check for updates
Copyright
© The Author(s), 2025. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aniol, CV, Prokop, JW, Rajasekaran, S et al. Dilated coronary arteries in a 2-month-old with RIT1-associated noonan syndrome: a case report. BMC Pediatr 2023; 23: 1.CrossRefGoogle Scholar
Gulati, GS, Gupta, A, Juneja, R, Saxena, A. Ectatic coronary arteries in Noonan syndrome. Tex Heart Inst J 2011; 38: 318–319.Google ScholarPubMed
Uçar, T, Atalay, S, Tekin, M, Tutar, E. Bilateral coronary artery dilatation and supravalvular pulmonary stenosis in a child with noonan syndrome. Pediatr Cardiol 2005; 26: 848–850.CrossRefGoogle Scholar
Calcagni, G, Baban, A, De Luca, E, Leonardi, B, Pongiglione, G, Digilio, MC. Coronary artery ectasia in noonan syndrome: report of an individual with SOS1 mutation and literature review. Am J Med Genet A 2016; 170: 665–669.CrossRefGoogle ScholarPubMed
Loukas, M, Dabrowski, M, Kantoch, M, Ruzyłło, W, Waltenberger, J, Giannikopoulos, P. A case report of noonan’s syndrome with pulmonary valvar stenosis and coronary aneurysms. Med Sci Monit 2004; 10: CS80–CS83.Google ScholarPubMed