Surgical Treatment of Superior Vena Cava Syndrome in a Preterm Neonate.

central venous catheter superior vena cava thrombosis

Journal

Vascular and endovascular surgery
ISSN: 1938-9116
Titre abrégé: Vasc Endovascular Surg
Pays: United States
ID NLM: 101136421

Informations de publication

Date de publication:
16 Sep 2024
Historique:
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 16 9 2024
Statut: aheadofprint

Résumé

Superior vena cava syndrome is rare and challenging clinical entity in neonates. Medical treatment options are usually effective. However, when failed, surgery is warranted. Herein, we present a preterm neonate with SVC syndrome and associated chylothorax. When 2 weeks old, he underwent successful open thrombectomy and SVC reconstruction under cardiopulmonary bypass. Immediately after the operation findings of SVC syndrome and chylotorax were completely resolved. To our knowledge, this patient is the smallest baby underwent open SVC reconstruction with cardiopulmonary bypass.

Identifiants

pubmed: 39283806
doi: 10.1177/15385744241284881
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15385744241284881

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Safak Alpat (S)

Division of Paediatric Cardiac Surgery, Department of Cardiovascular Surgery, Hacettepe University School of Medicine, Ankara, Turkiye.

Melih Alma (M)

Division of Paediatric Cardiac Surgery, Department of Cardiovascular Surgery, Hacettepe University School of Medicine, Ankara, Turkiye.

Classifications MeSH