The head, neck and spine

9 The head, neck and spine






ULTRASOUND TECHNIQUE


The routine cranial ultrasound for visualization of the intracranial contents in neonates is via the acoustic window created by the anterior fontanelle. This is the ‘soft area’ of the cranium and is generally only usefully open before the sutures have fused and the fontanelle becomes ossified at about 6–9 months. In conditions such as hydrocephalus where the sutures and therefore the anterior fontanelle remain open longer, the examination can be undertaken in an older infant. To obtain better views of the occipital horns of the lateral ventricles, the occipital parenchyma and the posterior fossa structures, scanning through the posterior and mastoid fontanelles is recommended. Good views of the circle of Willis can be obtained through the temporal window but with all these supplementary views image quality is dependent on bony thickness.


For good-quality cranial ultrasound a high-quality modern machine is needed with machine settings optimized for neonatal brain imaging with special presets. The best transducers to use are those that can fit snugly into the access provided by the anterior fontanelle and, generally, for an overall view of the intracranial contents, a vector 8V5 is best, but a small curvilinear transducer of high frequency is also very acceptable. Overriding sutures, small fontanelles and thick hair can sometimes be a problem and this is best overcome using a small transducer with copious gel. A high-frequency linear probe is very useful to examine the subarachnoid space and sagittal sinus. With new high-frequency linear transducers a stand-off pad is not necessary. It is important to use a transducer with sufficient power to be able to visualize the posterior fossa. The convention for orientating the images coronally is the same as for that of other cross-sectional imaging, such that the right hemisphere is on the left of the image. Sagittal scans should be orientated so that the face is on the left and the occiput on the right. Higher-frequency transducers may be needed for older infants and when accessing the intracranial structures via the supplementary views.


In the intensive care setting infants often have an endotracheal tube and lines in position. Nowadays they are usually secured in position by tying them to the bonnet in the infant. It is essential not to disturb these tubes and access to the anterior fontanelle should then be gained via a hole in the bonnet. Newborns are vulnerable to becoming cold, so it is best to examine them via the access holes in incubators and always to ensure that exposed infants remain warm.


A minimum of five coronal and five sagittal views are required for a standard examination, with additional views of the brain surface or any pathology found as required.


The availability of Doppler is extremely useful for the routine cranial examination. This is particularly true when trying to differentiate subdural from subarachnoid fluid in the subarachnoid spaces and in any suspected vascular lesion such as a vein of Galen anomaly. It has also been used in assessing vascular malformations post-embolization.1 Doppler ultrasound has been used to monitor the neonatal brain, in particular birth asphyxia, brain injury, hydrocephalus and brain death, with varying results. Transcranial Doppler in children with a closed fontanelle has been used in a limited way. They have been reportedly used in children with sickle cell anemia and to determine brain death.2




Measurements


There is an abundance of literature on intracranial measurements of the cerebral structures. The following describes the ventricles and subarachnoid measurements which are some of the most useful and widely used in clinical practise.



Ventricles


There is a large range of ventricular size, both prenatally and in the newborn. An integral part of the cranial ultrasound examination, in particular when ventricles are dilated, is a measure of the degree of dilation. There are many coronal and sagittal measurements quoted in the literature and these are just a confusing array for the uninitiated. It is important to have a standard technique and measurement for a department so that it is consistently reproducible between sonographers undertaking the examinations and so that the clinicians clearly understand the measurements produced. There is still no consensus as to which is best but the most universally accepted measure is the ventricular index as described by Levene. This chart is for preterm infants. The index measures the distance from the falx to the lateral border of the lateral ventricle. This is measured coronally in the plane of the third ventricle at the level of the foramen of Munro. The ‘ventricular index’ is measured as the largest distance between the frontal horns. Dividing this number by 2 results in the ‘ventricular index’. The measure is easy to understand and is reproducible. Clear visualization of the lateral ventricles can be obtained and landmarks clearly identified. It shows little interobserver error. The centile chart expressing the 3rd, 50th and 97th centiles from 26 to 42 weeks has been produced. The only problem with Levene’s ventricular index is when there is midline shift (Fig. 9.1). Measurements of ventricular size in term babies are shown as well.3 The author has also published similar charts for preterm babies.



According to Davies4 the ‘anterior horn width’ is the width of the anterior horn of the lateral ventricles measured in the 3D coronal view at the level of the foramen of Munro. The width is measured on each side as the distance between the medial wall and floor of the lateral ventricle at the widest point. The linear measurements taken in their study of infants with a mean age of < 33 weeks’ gestational age at birth were





The width of the ventricles may be expressed as a ratio of the total width of the cranium, the ventricles may be measured directly and now, with 3D techniques, volumetric measurements have all been reported. Using measurements expressed as a ratio does not reliably monitor growth and measurements of both ventricles and cortex may not even produce an abnormality when expressed as a ratio. Direct measurement of the ventricles is still the simplest, most reproducible and easy-to-teach technique.


The occipital poles enlarge before the body of the lateral ventricles, but measurements are unreliable and impractical due to the wide range of size and shape of the occipital horns. Measuring the biventricular diameter is also not reliable, as one ventricle may enlarge more rapidly than another (Box 9.1).





Normal anatomy


Cranial ultrasound examinations are performed in the coronal and sagittal planes (Fig. 9.4A,B). Additional acoustic windows are found through the temporal bone and mastoid fontanelle (Fig. 9.4C).







Axial planes

Axial planes are not routinely used but can be extremely useful if subdural or extra-axial fluid is suspected. Axial sections can be difficult to understand, so are best taken at the body of the lateral ventricles where anatomy is easily recognized (Fig. 9.5).


image image image image image image image image

Figure 9.5 Series showing normal anatomy MRI with ultrasound scans. (A) & (B) MRI scans at the level of the third ventricle to compare with the cranial ultrasound at the same level. The third ventricle (3) is a small slit-like structure in the midline below and between lateral ventricles. The connection with the lateral ventricles at the foramen of Munro (FoM) can be clearly seen and is an important landmark. The sylvian fissure (SF) is an important landmark laterally and becomes deeper the more posterior the scan. (C) Coronal scan at the level of the quadrigeminal cisterns just posterior to (B) showing the frontal horns of the lateral ventricles. There is a small cavum centrally and some echogenic choroid plexus in the floor of the lateral ventricles. (D) Moving the transducer posteriorly the lateral ventricles can be seen containing the echogenic choroid plexus (cp). Symmetry of the choroid can be assessed in this view. (E) Coronal section posteriorly over the sulci and gyri of the occipital lobes. The surface of the brain must be examined to assess for fluid collections and gyral pattern. (F) & (G) Midline sagittal MRI and ultrasound to compare the normal anatomy. This is a very useful image and can clearly demonstrate the echogenic cerebellar vermis (v), fourth ventricle (4) and third ventricle (3). The corpus callosum can be seen as a C-shaped structure just above the third ventricle. (H) Para-sagittal view of ventricle. This is a section through the lateral ventricle. The caudate nucleus (c) lies in the floor of the lateral ventricle and the caudothalamic groove is the landmark from which the choroid plexus (cp) inserts posteriorly. The caudate nucleus is more echogenic than the thalamus. The echogenic flare (flare) in the occipital white matter can be a normal finding.



The ventricular system

The ventricular system of the brain consists of two lateral ventricles, a third ventricle aqueduct of Sylvius and a fourth ventricle.


The lateral ventricles are the largest and consist of the frontal horn, the body, the temporal horn and the occipital horn. They all communicate and, in addition, they communicate with the subarachnoid spaces. They communicate with the third ventricle via the foramen of Munro and the fourth ventricle via the aqueduct of Sylvius. The third ventricle is not easy to see on the coronal scan as it is a slit-like structure, neither is the aqueduct on the sagittal scan. The fourth ventricle has the typical rhomboid ‘Napoleon’s hat shape’ and extends into the cerebellar vermis (Fig. 9.6).



Coarctation of the lateral ventricles is a normal variant, where there are cystic areas adjacent to the superolateral angle of the lateral ventricle at the level of the foramen of Munro. These cysts appear as a string of beads along the floor of the lateral ventricle. In some of the literature this is called subependymal pseudocysts. It is important not to confuse these with periventricular leukomalacia (Fig. 9.7).6










INTRACRANIAL HEMORRHAGE


The major cause of intracranial hemorrhage used to be trauma during delivery. Nowadays the major cause is prematurity, as the brain of the premature infant is highly susceptible to ischemia and hypoxia. Other causes include hypothermia, coagulopathy and pneumothoraces. One of the major roles of intracranial ultrasound is in the detection of hemorrhage, and the intracranial sites of hemorrhage are different depending on the etiology and age of the infant. The optimal time for scanning is 72 hours after birth. All periventricular hemorrhages occur after birth and within the first week of life, and the incidence of hemorrhage is directly related to prematurity.


All at-risk infants should have a scan by 7 days repeated at 14, as a small percentage will be missed on the first scan.


All infants under 34 weeks should be routinely scanned.


Bleeding may occur in a number of places related to the skull and intracranial contents. Fresh blood always appears highly echogenic. After a few weeks these intraparenchymal hemorrhagic areas may liquefy and become cystic.


The following should always be assessed:





Types of intracranial hemorrhage



Germinal matrix


This is a small area of brain occurring in the floors of the lateral ventricles and best seen on anterior coronal scans. This area is very vascular in the premature infant and that is why these hemorrhages occur primarily in the premature infant. It has a rich matrix of fragile capillaries and it is alterations in cerebral blood flow that causes vasodilation of these tiny vessels leading to hemorrhage. This may be an isolated finding but they occasionally will rupture into the ventricle and in a small percentage will rupture into the parenchyma through the roof of the lateral ventricle. By term and increasing gestational age the subependymal plate has almost completely disappeared. There is almost universally a good prognosis, with only a very small number (2%) reportedly resulting in neurological sequelae.8


Small germinal matrix hemorrhages, if they are fresh, appear echogenic. They may occasionally be mistaken for choroid in the floor of the lateral ventricle. Hemorrhages need to be confirmed in the sagittal view and occur anterior to the caudothalamic groove. There is no distortion of the ventricular system and after a number of weeks they may become cystic and eventually disappear as the brain grows (Fig. 9.9).









Subarachnoid hemorrhages


Subarachnoid hemorrhages may be due to blood in the ventricular system due to an intraventricular hemorrhage or from a bleeding diathesis and bleeding from the vessels. Other causes include passive dilation of the subarachnoid space, which may be due to brain atrophy, subdural effusion or abscess which may develop as a result of meningitis and subdural hemorrhages at various stages. Visualization of the cortical veins and their branches within fluid collections around the brain suggest that the pericerebral collection is caused by an enlarged subarachnoid space and not a subdural. This is best demonstrated with color Doppler to show the flow in superficial cortical vessels which lie along the superficial gyri and sulci.


Differentiation of subdural and subarachnoid hemorrhages can be difficult on ultrasound (Fig. 9.10) (Table 9.2).



Table 9.2 Differentiation of subdural and subarachnoid hemorrhages









Subdural Subarachnoid




Classification


There is no internationally accepted grading system for germinal matrix hemorrhage/intraventricular hemorrhage (GMH–IVH). Tables 9.3 and 9.4 outline the grading systems for periventricular hemorrhage used for ultrasound scanning.


Table 9.3 Grading system for PVH used or adapted for use with ultrasound brain scanning9















Grade I Isolated SEH
Grade II Rupture into ventricle, but no dilation
Grade III Rupture into ventricle with dilation
Grade IV IVH with parenchymal extension

IVH, intraventricular hemorrhage; SEH, subependymal hemorrhage.


Table 9.4 A modification of the grading system suggested by Levene and de Crespigny14





































HEMORRHAGE
0 No hemorrhage
1 Localized hemorrhage <1 cm in its largest measurement
2 Hemorrhage >1 cm in its largest measurement but not extending beyond the atrium of the lateral ventricle
3 Blood clot forming a cast of the lateral ventricle and extending beyond the atrium
4 Intraparenchymal hemorrhage
VENTRICULAR DILATION
0 No dilation
1 Transient dilation
2 Persistent but stable dilation
3 Progressive ventricular dilation requiring treatment
4 Persistent asymmetrical ventricular dilation

The advantage of Papille’s grading system is that it is simple and easy to understand.9 Levene’s grading system has also gained some acceptance but it is more complicated and neither take account of periventricular leukomalacia.13


It is far better to document the site and size of the hemorrhage and, if there is ventricular dilation, to measure it (Fig. 9.11).










PERIVENTRICULAR LEUKOMALACIA (PVL)


This is a condition primarily occurring in the premature infant and is associated with hypoxic-ischemic brain insult. During the weeks 32–34 there are many changes in the cerebral vasculature with disappearance of the germinal matrix and rapid growth of the cortex and white matter. There is a marked increase in the vascular and oxygen requirement to these areas. PVL is then related to a lack of oxygen (hypoxia) or a reduction in cerebral perfusion (ischemia).


PVL may occur some time after birth and in some reported series up to 11 weeks. The causes of PVL are primarily prenatal events such as abruptio placenta, twin-to-twin transfusion and perinatal birth asphyxia, recurrent apnea, cardiac arrest and shock, severe respiratory distress syndrome (RDS) in the premature, and perinatal asphyxia in the newborn.


PVL is characterized by multiple periventricular infarcts and necrosis affecting the white matter and sparing the gray matter. It describes the cystic changes that affect the white matter typically in the watershed areas which are affected by ischemia. The white matter usually affected is anterior to the frontal horns, the external angle of the lateral ventricles and the lateral surface of the occipital horns.


Dec 21, 2015 | Posted by in PEDIATRIC IMAGING | Comments Off on The head, neck and spine

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