The atrium of the lateral ventricle (measured at the level of the glomus of the choroid plexus, across the atria) is normally <10 mm. Ventriculomegaly is diagnosed when the atrial diameter is ≥10 mm.
Classification (based on atrial width)
- Mild (borderline): 10–12 mm
- Moderate: 13–15 mm
- Severe: >15 mm (sometimes called hydrocephalus when progressive and associated with increased head size/intracranial pressure)
Ultrasound report line (Findings):Each Lateral ventricles are markedly dilated measuring >15 mm at the atrial level, with ballooning of the ventricular atria, consistent with severe ventriculomegaly.
Right atria:15.0 mm
Left atria:17.5 mm
Conclusion: Severe Ventriculomegaly
Recommendation: Detailed fetal neurosonography and anomaly scan to assess associated CNS and extra-CNS anomalies.
Consider fetal MRI for further evaluation of brain parenchyma and associated anomalies.
Recommend counseling and evaluation for possible chromosomal, genetic, or TORCH infectious etiologies.
Etiology / Causes
Ventriculomegaly can be isolated or associated with other abnormalities:
- Obstructive causes
- Aqueductal stenosis
- Neural tube defects (spina bifida, encephalocele)
- Masses (tumors, hemorrhage, arachnoid cyst)
- Non-obstructive causes
- Chromosomal abnormalities (e.g., Trisomy 21, 18, 13)
- Congenital infections (CMV, toxoplasmosis, Zika virus)
- Cortical malformations (agenesis of corpus callosum, holoprosencephaly, lissencephaly)
- Brain atrophy from ischemic/hemorrhagic injury
- Lateral ventricle atrium >10 mm, measured in axial plane at level of thalami and cavum septi pellucidi.
- Dangling choroid plexus sign (choroid plexus appears to “hang” within enlarged ventricle).
- Assess for associated findings:
- Intracranial anomalies (corpus callosum agenesis, Dandy–Walker malformation)
- Extracranial anomalies
- Fetal growth restriction
- Signs of infection (calcifications, microcephaly)
Prognosis
- Isolated mild ventriculomegaly (10–12 mm): ~80–90% have normal neurodevelopmental outcome.
- Moderate (13–15 mm): Outcome depends on progression and associated anomalies; ~60–70% normal if isolated.
- Severe (>15 mm): High risk of neurodevelopmental impairment, motor/cognitive deficits, or death.
Evaluation / Work-up
- Detailed fetal neurosonography (evaluate for structural CNS malformations).
- Fetal MRI (to assess cortical and midline structures).
- Genetic testing (amniocentesis with karyotype and microarray).
- TORCH screening for intrauterine infections.
- Serial ultrasounds to monitor progression.
Evaluation / Work-up
- Detailed fetal neurosonography (evaluate for structural CNS malformations).
- Fetal MRI (to assess cortical and midline structures).
- Genetic testing (amniocentesis with karyotype and microarray).
- TORCH screening for intrauterine infections.
- Serial ultrasounds to monitor progression.
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