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A systematic review of prenatally diagnosed vein of Galen malformations: prenatal predictive markers and management from fetal life to childhood.
Di Meglio, Lavinia; Sica, Giordana; Toscano, Paolo; Orlandi, Giuliana; Manzo, Luigi; Mazzarelli, Laura Letizia; Sica, Carmine; Di Meglio, Aniello.
Afiliación
  • Di Meglio L; Residency School of Pediatrics, University of Rome Tor Vergata, Rome, Italy.
  • Sica G; University of Medicine and Surgery Luigi Vanvitelli, Naples, Italy.
  • Toscano P; Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine and Surgery Federico II of Naples, Naples, Italy.
  • Orlandi G; Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine and Surgery Federico II of Naples, Naples, Italy.
  • Manzo L; Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine and Surgery Federico II of Naples, Naples, Italy.
  • Mazzarelli LL; Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine and Surgery Federico II of Naples, Naples, Italy.
  • Sica C; Diagnositica Ecografia e Prenatale di A. Di Meglio, Naples, Italy.
  • Di Meglio A; Diagnositica Ecografia e Prenatale di A. Di Meglio, Naples, Italy.
Front Pediatr ; 12: 1401468, 2024.
Article en En | MEDLINE | ID: mdl-39022219
ABSTRACT

Introduction:

Vein of Galen malformations (VGMs) account for less than 1% of all intracranial vascular malformations. However, in fetal and pediatric populations, they represent the most common vascular malformation of the brain. For the effective management of this condition, an optimal knowledge of its prenatal and postnatal clinical features is mandatory.

Methods:

Articles published between 1 January 2003 and 31 January 2024, reported in PubMed and EMBASE, were evaluated for a systematic review analyzing the prenatal and postnatal features and management of fetal VGMs.

Results:

Thirty-one papers reporting information on 51 prenatally diagnosed VGMs were included. The most common prenatal features were fetal hydrocephalus (39%) and cardiomegaly (56%). Postnatal data for 43 VGM cases are described. The overall mortality was 58.14%. In total, 77.78% of the survivors had normal development.

Conclusions:

Close follow-up and a multidisciplinary approach are mandatory to manage this condition. Our study aimed to provide a guide for gynecologists, neonatologists, cardiologists, and neuroradiologists.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza