Macrocephaly Secondary to Superior Vena Cava Syndrome.


Journal

Pediatric neurosurgery
ISSN: 1423-0305
Titre abrégé: Pediatr Neurosurg
Pays: Switzerland
ID NLM: 9114967

Informations de publication

Date de publication:
2020
Historique:
received: 09 05 2019
accepted: 03 09 2019
pubmed: 19 2 2020
medline: 11 11 2020
entrez: 19 2 2020
Statut: ppublish

Résumé

Cardiac defects in neonates are often associated with neurological or neuroanatomical anomalies. We present a patient who developed macrocephaly secondary to superior vena cava syndrome, resultant from repair of her congenital tetralogy of Fallot. She was managed conservatively with serial imaging and close observation from the neurosurgical aspect, and her head growth stabilized without requiring ventriculoperitoneal shunting after stent placement in her superior vena cava. In patients with macrocephaly secondary to cardiac issues, cerebrospinal fluid diversion is often performed quickly. For our patient - who had no obvious signs of worsening intracranial hypertension or symptoms beyond macrocephaly - treatment of her overall cardiovascular issues was successful in achieving stability of her head circumference growth.

Identifiants

pubmed: 32069465
pii: 000503111
doi: 10.1159/000503111
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

42-45

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Pouya Entezami (P)

Department of Neurosurgery, Albany Medical Center, Albany, New York, USA.

Amanda Custozzo (A)

Department of Neurosurgery, Albany Medical Center, Albany, New York, USA.

Matthew Adamo (M)

Department of Neurosurgery, Albany Medical Center, Albany, New York, USA, adamom@amc.edu.

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Classifications MeSH