The central nervous system

2 The central nervous system





Cerebral cortex (Figs 2.1, 2.2)


The superolateral surface of each cerebral hemisphere has two deep sulci; these are:






The parieto-occipital sulcus on the medial surface of the hemisphere separates the parietal and occipital lobes. On the lateral surface of the hemispheres there is no complete sulcal separation of the parietal, temporal and occipital lobes. The boundary between the parietal and temporal lobes lies on a line extended back from the lateral sulcus. The boundary separating the parietal and temporal lobes from the occipital lobe is a line between the superior border of the parieto-occipital sulcus and the preoccipital notch (see Fig. 2.1).








Radiological features of the cerebral cortex



CT and MRI


Identification of lobes on CT slices depends on identification of their boundaries. The sylvian cistern and fissure separating the frontal and temporal lobes are easily identified on axial CT or MR slices (Fig. 2.3). The central sulcus that forms a boundary between the frontal and parietal lobes is less well seen, however. This lies at a transverse level just posterior to the anterior limit of the lateral ventricles. Because CT images are obtained parallel to the canthomeatal line, on upper images the central sulcus is quite posterior in position. On axial images it has been described as having an inverted omega shaped curve that marks the position of the hand motor cortex (Fig. 2.3D).



The parieto-occipital sulcus on the medial surface of the hemisphere can be seen on CT at the level of the lateral ventricles and on midline sagittal MR images (see Fig. 2.5). The parieto-occipital junction on the lateral surface has no anatomical landmark but lies at approximately the same transverse level as the sulcus.


Midline sagittal images also show the cingulate gyrus and callosal and cingulate sulci. The insula and the frontal, parietal and temporal opercula can be seen on axial CT and on MR imaging in all planes.




White matter of the hemispheres


There are three types of fibre within the cerebral hemispheres:






Commissural fibres



The corpus callosum (Figs 2.4, 2.5)


The corpus callosum is a large midline mass of commissural fibres, each of which connects corresponding areas of both hemispheres. It is approximately 10 cm long and becomes progressively thicker towards its posterior end. Named parts include the following:








In cross-section, fibres from the genu that arch forward to the frontal cortex on each side are called forceps minor, and fibres from the splenium passing posteriorly to each occipital cortex are called forceps major. Fibres extending laterally from the body of the corpus callosum are called the tapetum. These form part of the roof and lateral wall of the lateral ventricle.








Radiological features of the commissural and projection fibres




CT and MRI


The corpus callosum cannot be well seen on axial CT slices. The internal capsule is seen as a V-shaped low-attenuation or high T1 signal structure (see Fig. 2.3C) between the caudate and lentiform nuclei anteriorly and the lentiform and thalamus posteriorly.


The rostrum, genu, body and splenium can be seen on sagittal MRI (Fig. 2.5). The anterior and posterior commissures can also be seen on this view. A line joining the anterior and posterior commissures, the AC–PC line, is used as a reference in image-guided procedures.


On coronal MRI scans (Fig. 2.7) the body of the corpus callosum and the tapetum can be seen superior to the lateral ventricles and the internal capsule can be seen lateral to the thalami. On this view the anterior commissure may also be visible inferior to the third ventricle, but this commissure is best seen as an arc of fibres on axial MRI (Fig. 2.6).





Radiology pearl


Unmyelinated immature white matter because of its higher water content is darker on T1 sequences and brighter on T2 sequences than mature myelinated white matter. The progression of myelination can therefore be seen on MRI of infants. This progresses in a predictable way from deep to superficial, from posterior to anterior and from inferior to superior (Fig. 2.8)



MR tractography is a technique that uses diffusion tensor imaging to obtain images of fibre tracts within the brain. These scans also give information about fibre direction (Fig. 2.9).





Basal ganglia (Figs 2.11, 2.12)


This subcortical grey matter includes:











Radiological features of the basal ganglia





Thalamus, hypothalamus and pineal gland


The structures around the third ventricle include the thalamus, hypothalamus and pineal gland. Together with the habenula these form the diencephalon.



Thalamus


These paired, ovoid bodies of grey matter lie in the lateral walls of the third ventricle, from the interventricular foramen anteriorly to the brainstem posteriorly. Each has its apex anteriorly and a more rounded posterior end called the pulvinar. The thalamus is related laterally to the internal capsule and, beyond that, to the lentiform nucleus. The body and tail of the caudate nucleus are in contact with the lateral margin of the thalamus. The superior part of the thalamus forms part of the floor of the lateral ventricle.


The thalamus is attached in approximately 60% of cases to the thalamus of the other side, across the third ventricle by the interthalamic adhesion or massa intermedia. This is not a neural connection.


Most thalamic nuclei are relay nuclei of the main sensory pathways. Medial and lateral swellings on the posteroinferior aspect of the thalamus are called the geniculate bodies. The medial geniculate body is attached to the inferior colliculus and is involved in the relay of auditory impulses. The lateral geniculate body is attached to the superior colliculus and is involved with visual impulses. The thalamus receives its blood supply from thalamostriate branches of the posterior cerebral artery.


Separate to and below the thalami are paired nuclei called the subthalamic nuclei (Fig. 2.7B) which are connected to the lateral putamen and the substantia nigra. Their function is unknown but destruction of one of them causes hemiballismus.






Radiological features of the thalamus, hypothalamus and pineal gland




CT and MRI


The structures forming the hypothalamus can best be appreciated on midline sagittal MRI (Fig. 2.5). The optic chiasm, the tuber cinereum, the infundibular stalk and the interpeduncular cistern, containing the mamillary bodies and in the base of which lies the posterior perforated substance, can be identified. The thalami can be seen on axial images on each side of the third ventricle (Fig. 2.3C). Their relationship to the posterior limb of the internal capsule and to the lentiform nucleus can be appreciated on this slice. The pineal gland and its superior and inferior laminae can also be best seen on midline sagittal MRI. Subthalamic nuclei can best be seen on coronal MRI (Fig. 2.7B).




Pituitary gland (Fig. 2.14)


The pituitary gland (hypophysis cerebri) lies in the pituitary fossa and measures 12 mm in its transverse diameter, 8 mm in its anteroposterior diameter and 9 mm high.



The pituitary gland has a hollow stalk, the infundibulum, which arises from the tuber cinereum in the floor of the third ventricle. This stalk is composed of nerve fibres whose cell bodies are in the hypothalamus. It is directed anteroinferiorly and surrounded by an upward extension of the anterior lobe, the tuberal part.


The anterior lobe is five times larger than the posterior lobe. It is developed from Rathke’s pouch in the roof of the primitive mouth. (A tumour from remnants of the epithelium of this pouch is called a craniopharyngioma.) The anterior lobe produces hormones in response to release factors carried from the hypothalamus by hypophyseal portal veins.


The posterior lobe is made up of nerve fibres whose cell bodies lie in the hypothalamus and release hormones in response to impulses from these nerves.


The anterior lobe is adherent to the posterior lobe by a narrow zone called the pars intermedia. This is, in fact, developmentally and functionally part of the anterior lobe.


The relations of the pituitary gland are as follows:





The cavernous sinuses are united by intercavernous sinuses, which surround the pituitary gland anteriorly, posteriorly and inferiorly.




Radiological features of the pituitary gland




MRI (Fig. 2.14)


Sagittal and coronal images are most useful. The size and shape of the normal pituitary gland varies. In adult males the gland ranges from 8 to 10 mm craniocaudad dimension in the sagittal plane. The dura above the sella should be horizontal, not convex. In females, the size of the gland varies with the menstrual cycle and pregnancy. In the post-partum period it may normally exceed 12 mm in height. It is also normal for the gland to have a convex upper border in menstruating or lactating females. During puberty, the gland may also have an convex upper surface in both males and females.


In normal adults the anterior pituitary occupies 70–80% of the total gland volume and is isointense to cerebral white matter on T1 images. The posterior pituitary usually has high signal intensity on unenhanced T1 images due to the effect of stored neurosecretory granules on the T1 relaxation time. This so-called posterior pituitary bright spot is evident in up to 90% of children but is less consistently observed in adults. The pars intermedia, a vestigial remnant of Rathke’s pouch, is not normally visualized on imaging studies. In some cases, a small cyst may mark the location of the pars intermedia.


The infundibulum tapers from the floor of the third ventricle to the pituitary gland. The diameter of the infundibulum should be no bigger than 3 mm or the adjacent basilar artery. The sella itself is delineated by signal void of the bony cortex and by the high-intensity signal of marrow in the clivus. The optic nerves and chiasm and the intracranial carotid vessels above, and the sphenoid sinus below, are seen clearly on coronal sections.



Dec 19, 2015 | Posted by in PEDIATRIC IMAGING | Comments Off on The central nervous system

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