Not all ventriculomegaly is created equal: diagnostic overview of fetal, neonatal and pediatric ventriculomegaly
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Pediatric Hydrocephalus 22 items
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Read the article on pubmed.ncbi.nlm.nih.gov ↗Article · Nov 2019 · 1 min read
In brief
In brief
This comprehensive review examines fetal, neonatal, and pediatric ventriculomegaly, covering diagnostic approaches from prenatal ultrasound through fetal MRI, associated CNS abnormalities, and treatment strategies. The authors discuss how etiology and severity impact clinical outcomes and present institutional data tracking prenatally diagnosed cases through the perinatal period.
Written by the GCMD Library team from the article.
Fetal ventriculomegaly refers to a condition in which there is enlargement of the ventricular spaces, typically on prenatal ultrasound. It can be associated with other CNS or extra-CNS abnormalities, and this relationship is crucial to understand as it affects overall neonatal outcome. Isolated ventriculomegaly has been described in the literature with variable clinical outcome. Typically, outcome is based on the etiology and degree of ventriculomegaly. When associated with a pathologic condition, ventriculomegaly can be a result of hydrocephalus. While initial diagnosis is usually made on prenatal ultrasound, fetal magnetic resonance imaging is preferred to further elucidate any associated CNS malformations. In this paper, the authors aim to provide a comprehensive review of the diagnosis, associated etiologies, prognosis, and treatment options related to fetal, neonatal, and pediatric ventriculomegaly and hydrocephalus. In addition, preliminary data is provided from our institutional cohort of patients with a prenatal diagnosis of ventriculomegaly followed through the perinatal period.
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