Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-23T06:28:28.591Z Has data issue: false hasContentIssue false
  • English
  • Français

Acute aortic dissection in a patient with Williams syndrome infected by COVID-19

Published online by Cambridge University Press:  12 October 2020

Setareh Mamishi ,
Ameneh Navaeian  and
Reza Shabanian Open the ORCID record for Reza Shabanian [Opens in a new window]
Setareh Mamishi
Affiliation:
Department of Pediatric Infectious Diseases, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran Department of Infectious Diseases, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
Ameneh Navaeian
Affiliation:
Department of Pediatric Infectious Diseases, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
Reza Shabanian*
Affiliation:
Department of Pediatric Cardiology, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
*
Author for correspondence: Reza Shabanian, Children’s Medical Center, 63 Gharib Street, 1419733151, Tehran, Iran. Tel: +98 9122987428; Fax: +98 21 66930024. E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Cardiovascular involvement in COVID-19 has different features. Here we report the ominous fate of a neglected adolescent with Williams syndrome that was infected by SARS-CoV-2 and ended by acute aortic dissection.

Keywords

Williams syndromeaortic dissectionCOVID-19aortitis
Type
Brief Report
Information
Cardiology in the Young , Volume 31 , Issue 1 , January 2021 , pp. 132 - 134
Check for updates
Copyright
© The Author(s), 2020. 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

Collins, RT. Cardiovascular disease in Williams syndrome. Circulation 2013; 127: 2125–2134.CrossRefGoogle ScholarPubMed
Riphagen, S, Gomez, X, Gonzalez-Martinez, C, Wilkinson, N, Theocharis, P. Hyperinflammatory shock in children during COVID-19 pandemic. Lancet 2020; 395: 1607–1608.CrossRefGoogle ScholarPubMed
Simpson, TF, Kovacs, RJ, Stecker, EC. Ventricular arrhythmia risk due to hydroxychloroquine-azithromycin treatment for COVID-19. Cardiol Mag 2020; 29: 29.Google Scholar
Collins, RT. Clinical significance of prolonged QTc interval in Williams syndrome. Am J Cardiol 2011; 108: 471–473.CrossRefGoogle ScholarPubMed
Fukunaga, N, Fujiwara, H, Nasu, M, Okada, Y. Aortic dissection caused by aortitis associated with hepatitis C virus-related cryoglobulinemia. J Thorac Cardiovasc Surg 2010; 140: e81–e82.10.1016/j.jtcvs.2010.07.021CrossRefGoogle ScholarPubMed
Vanacker, P, Thijs, V. Spontaneous cervical artery dissection in adult Williams syndrome. Cerebrovasc Dis 2009; 27: 309–310.CrossRefGoogle ScholarPubMed
Wei, HY, Chung, HT, Wu, CT, Huang, JL. Aortic dissection complicated with hemothorax in an adolescent patient with systemic lupus erythematosus: case report and review of literature. Semin Arthritis Rheum 2011; 41: 12–18.10.1016/j.semarthrit.2010.08.002CrossRefGoogle Scholar
Spigset, O. Drug-induced aortic aneurysms, ruptures and dissections. In: Grundmann, R (ed). Etiology, Pathogenesis and Pathophysiology of Aortic Aneurysms and Aneurysm Rupture. InTech, Croatia, 2011; 159–174.Google Scholar