Macrocephaly Secondary to Superior Vena Cava Syndrome.
Macrocephaly
Superior vena cava syndrome
Tetralogy of Fallot
Journal
Pediatric neurosurgery
ISSN: 1423-0305
Titre abrégé: Pediatr Neurosurg
Pays: Switzerland
ID NLM: 9114967
Informations de publication
Date de publication:
2020
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
42-45Informations de copyright
© 2020 S. Karger AG, Basel.