Hemopericardium with cardiac tamponade as a rare presentation of a massive aortic aneurysm in a young child with autosomal recessive cutis laxa.


Journal

Echocardiography (Mount Kisco, N.Y.)
ISSN: 1540-8175
Titre abrégé: Echocardiography
Pays: United States
ID NLM: 8511187

Informations de publication

Date de publication:
12 2021
Historique:
revised: 01 11 2021
received: 02 09 2021
accepted: 08 11 2021
pubmed: 1 12 2021
medline: 27 1 2022
entrez: 30 11 2021
Statut: ppublish

Résumé

Aortic aneurysms are rare in the pediatric age group and are commonly caused by genetic disorders associated with vasculopathy, weakness and fragility of arterial walls with progressive dilatation or even rupture. We reported a giant aortic aneurysm involving the ascending aorta and aortic arch in a 20-month-old girl with autosomal recessive cutis laxa type 1B (ARCL1B) who presented with hemorrhagic pericardial effusion and tamponade (impending rupture). Successful surgical repair has been done through excision of the aneurysmal part and replacement by Hemashield graft with preservation of the aortic valve.

Identifiants

pubmed: 34845761
doi: 10.1111/echo.15263
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

2095-2099

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

Loeys B, De Paepe A, Urban Z, EFEMP2-related Cutis Laxa. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, et al., editors. Seattle (WA); 1993.
Letard P, Schepers D, Albuisson J, et al. Severe phenotype of Cutis Laxa Type 1B with antenatal signs due to a novel homozygous nonsense mutation in EFEMP2. Mol Syndromol. 2018;9:190-196.
Beyens A, Boel A, Symoens S, Callewaert B. Cutis laxa: a comprehensive overview of clinical characteristics and pathophysiology. Clin Genet. 2021;99:53-66.
Hibino M, Sakai Y, Kato W, et al. Ascending aortic aneurysm in a child with fibulin-4 deficiency. Ann Thorac Surg [Internet]. 2018;105:e59-e61.
Deshpande S, Alazraki A, Khoshnam N, et al. Four new cases of pediatric thoracic aortic aneurysm (TAA) with review of the molecular genetic basis, utilizing the newly published consensus nomenclature. Cardiovasc Pathol [Internet]. 2017;31:34-40.
Yetman AT, Hammel J, Sanmann JN, Starr LJ. Valve-sparing root and total arch replacement for Cutis Laxa aortopathy. World J Pediatr Congenit Hear Surg. 2019;10:376-379.
Szabo Z, Crepeau MW, Mitchell AL, et al. Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene. J Med Genet. 2006;43:255-258.

Auteurs

Khadijah Maghrabi (K)

Paediatric Cardiology Division, Department of Pediatrics, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.

Osman Al-Radi (O)

Cardiac Surgery Division, Department of Surgery, King Abdulaziz University, Jeddah, Saudi Arabia.

Gaser Abdelmohsen (G)

Paediatric Cardiology Division, Department of Pediatrics, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.
Paediatric Cardiology Division, Department of Pediatrics, Kasr Al Ainy School of Medicine, Cairo University, Cairo, Egypt.

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Classifications MeSH