Annuloplasty for Aortic Regurgitation in Infantile Takayasu Arteritis: A Case Report.


Journal

World journal for pediatric & congenital heart surgery
ISSN: 2150-136X
Titre abrégé: World J Pediatr Congenit Heart Surg
Pays: United States
ID NLM: 101518415

Informations de publication

Date de publication:
Jul 2020
Historique:
pubmed: 5 7 2017
medline: 26 1 2021
entrez: 5 7 2017
Statut: ppublish

Résumé

Aortic regurgitation (AR) is a life-threatening complication of Takayasu arteritis (TA). Takayasu arteritis is a large-vessel vasculitis with a predominance in young adolescent and adult females. Inflammation involves the aorta and its major branches resulting in arterial dilatation, stenosis, aneurysm, occlusion, and thrombosis formation. Pediatric TA cases have been reported to also cause severe complications such as coronary aneurysms, retinopathy, and hypertension due to renovascular stenosis. In this report, we present a rare occurrence of infantile TA with severe AR requiring surgical intervention after failing medical therapy. Due to the patient's age and clinical status, a valve-sparing aortic annuloplasty with aortoplasty was performed.

Identifiants

pubmed: 28673107
doi: 10.1177/2150135117692979
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

NP31-NP33

Auteurs

Laura Linnemeier (L)

Deparment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.

Richa Sharma (R)

Deparment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.

Nayan Srivastava (N)

Deparment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Pediatric Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.

Mark Turrentine (M)

Deparment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Cardiovascular and Thoracic Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.

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Classifications MeSH