Topic 11 - cranial ultrasound Flashcards
Why is abnormal development of the brain common?
- Because of the complexity of its embryologic history, abnormal development of the brain is common (approximately 3 of 1000 births).
- Most major birth defects result from defective closure of the rostral neuropore
What is an encephalocele?
- herniation of intracranial contents resulting from a defect in the cranium
- most common in the occipital region
- The hernia may contain meninges (meningocele)
- meninges and part of the brain (meningoencephalocele)
- or meninges, part of the brain, and part of the ventricular system (meningohydroencephalocele) .
What is meroencephaly?
- severe defect of the calvaria and brain that results from failure of the rostral neuropore to close during the fourth week.
- The forebrain, midbrain, and most of the hindbrain and calvaria are absent
- Most of the embryo’s brain is exposed or extruding from the cranium (exencephaly) .
- The remains of the brain appear as a spongy, vascular mass consisting mostly of hindbrain structures.
- a common lethal defect , occurring in at least 1 of 1000 births.
- it is always associated with acrania (complete or partial absence of neurocranium).
- It may be associated with rachischisis ( failure of fusion of neural arches) when defective neural tube closure is extensive
What is microcephaly?
- neurodevelopmental disorder .
- The calvaria and brain are small, but the face is normal sized
- These infants are grossly mentally deficient because the brain is underdeveloped.
What causes microcephaly?
- Microcephaly is the result of a reduction in brain growth .
- Inadequate pressure from the growing brain leads to the small size of the neurocranium (bones of cranium)
What is agenesis of the corpus callosum?
- there is a complete or partial absence of the corpus callosum
- which is the main neocortical commissure of the cerebral hemispheres
- The condition may be asymptomatic, but seizures and mental deficiency are common.
- Agenesis of the corpus callosum is associated with more than 50 human congenital syndromes.
What can cause hydrocephalus?
- impaired circulation and absorption of CSF and, in rare cases, from increased production of CSF by a choroid plexus adenoma (benign tumor).
- A premature infant may develop intraventricular hemorrhage leading to hydrocephalus through the obstruction
- Rarely, impaired CSF circulation results from congenital aqueductal stenosis
What happens to the cranium when hydrocephalus occurs in neonates?
- Blockage of CSF circulation results in dilation of the ventricles proximal to the obstruction, internal accumulation of CSF , and pressure on the cerebral hemispheres
- This squeezes the brain between the ventricular fluid and the neurocranium.
- In infants, the internal pressure results in an accelerated rate of expansion of the brain and neurocranium because most of the fibrous sutures are not fused
What is non obstructive hydrocephalus?
• Hydrocephalus resulting from obliteration of the subarachnoid cisterns or malfunction of the arachnoid villi is called nonobstructive or communicating hydrocephalus .
How does the appearance of the premature brain differ from the term brain?
- lateral ventricles are slightly larger
- cavum septi pellucidi extends back to become the cavum vergae between the lateral ventricle bodies and occipital horns.
- There are only a few sulci, and the sylvian fissures are wider and typically appear boxlike rather than as thin fissures.
- The basal ganglia in premature infants are normally diffusely homogeneously echogenic, an appearance that is more prominent than in the thalami and typically more echogenic than the cerebral cortex.
- Basal ganglia and thalami do not show increased echogenicity at term-equivalent age.
What are some normal anatomical variants?
- cavum septum pellucidum and vergae
- choroid plexus cysts
- extra axial fluid
- sulcal variations according to gestational age.
Describe the persistent fetal fluid filled spaces
- The CSP is a midline fluid-filled space located anteriorly and between the frontal horns of the lateral ventricles
- formed from failed septal laminae fusion
- If the space extends posterior to the fornices, it is termed cavum vergae.
- A cavum veli interpositi is located even further posteriorly as a separate fluid-filled space found in the pineal region.
- Due to the location of the cavum veli interpositi. It must be distinguished from other commonly occurring manifestations in this region, specifically, congenital pineal cysts and vein of Galen malformations
How does brain sulcation change over time?
- The infant brain becomes increasingly sulcated during development.
- Cerebral cortices in neonates born prior to the 24th week gestational age contain only Sylvian fissures in an otherwise smooth cerebral cortex making lissencephaly in this age group an avoidable diagnosis
- At 24 weeks gestational age, the parietooccipital fissure is seen.
- This is followed by the appearance of the cingulate sulci at 28 weeks gestational age with additional branching occurring into full term
How does choroid plexus appear on ultrasound?
- The choroid plexus is located at the roof of the third ventricle and travels through the foramen of Monro into the lateral ventricles
- It does not extend into the frontal or occipital horns
- so hyperechoic material in these areas should suggest pathology.
- Choroid appearing substance anterior to the caudothalamic groove is likely a germinal matrix hemorrhage
- while interventricular hemorrhage may be indicated by hyperechoic material in the dependent portions of the occipital horns
How do you differentiate normal choroid from haemorrhage?
• Color Doppler ultrasound will differentiate the normal highly vascular choroid from similarly echogenic, but avascular, clot