Cerebral hemispheres and white matter tracts


Core procedures

  • Treatment of medically refractory epilepsy.

This chapter will address the key surgically relevant cortical and white matter anatomy of the brain and some of the principles underlying resection of limbic/paralimbic gliomas and removal of tumours in the eloquent cortex.

Clinical anatomy

Osseous anatomy and landmarks

Sutures

The cranial vault (calvaria) encloses the meninges and central nervous tissue. It consists of single frontal and occipital bones and bilateral parietal bones. The greater wings of the sphenoid bone and the squamous parts of the temporal bones enclose it laterally. These bones articulate at a series of fibrous sutures. The coronal suture separates the squamous frontal bone from each parietal bone across the midline. The sagittal (interparietal) suture begins at the bregma (the meeting point between the frontal and two parietal bones) and continues in the midline perpendicular to the coronal suture. It terminates at the lambda, which is the most apical point of the occipital bone. The lambdoid suture runs laterally and inferiorly from the lambda to form an approximately equilateral triangle between the parietal and occipital bones. At its most lateral and inferior aspect, the coronal suture terminates in a region known as the pterion. Here it meets the apex of the sphenofrontal suture, which separates the frontal bone from the greater wing of sphenoid, at an oblique angle. The sphenofrontal suture continues posteriorly as the sphenoparietal suture, separating the superior plateau of the greater sphenoid wing from the inferior edge of the parietal bone. The sphenoparietal suture terminates abruptly at the point where the sphenoid, parietal and temporal bones meet. From this point, the posterior edge of the greater sphenoid wing and anterior edge of the temporal bone are separated by the sphenosquamous suture. The parietal bone and the superior edge of the temporal bone are separated by the squamosal suture, which assumes an arc-like trajectory across the lateral aspect of the skull. Towards its posterior edge, the squamous suture plateaus and continues posteriorly to meet the obliquely travelling lambdoid suture. This plateau is the parietomastoid suture, which separates the parietal bone from the mastoid portion of the temporal bone. The asterion is defined as the junction of the parietomastoid, occipitomastoid and lambdoid sutures.

Bony landmarks

The nasion is the midline bony depression inferior to the glabella, demarcating the junction of the frontal and bilateral nasal bones. The external occipital protuberance or inion is found in the sagittal plane posteriorly: surgically, it is a landmark for the torcular Herophili or confluence of the superior sagittal, straight, occipital and transverse venous sinuses. Several landmarks may be located using the nasion and inion as geographical landmarks together with imaginary lines. Kocher's point is a parasagittal landmark, 11 cm posterior and 2–3 cm lateral to the nasion, used as a guide for catheter placement into the frontal horn. Frazier's point, used for catheter placement into the posterior aspect of the lateral ventricle, is found 6–7 cm above and 3–4 cm lateral to the inion. Keen's point is located 3 cm superior and 3 cm posterior to the top of the pinna and is used for catheter placement into the lateral aspect of the lateral ventricle, as commonly undertaken during paediatric ventriculoperitoneal shunt placement.

Cortical anatomy

The cerebral hemispheres are separated in the midline by the sagittal or interhemispheric fissure, running from the frontal pole to the occipital pole. Viewed laterally, the central sulcus separates the frontal and parietal lobes. It runs perpendicularly on either side of the interhemispheric fissure and passes obliquely, coronally and anteriorly before terminating inferiorly at the Sylvian (lateral) fissure. The primary motor cortex lies immediately anterior to the central sulcus; the primary sensory cortex lies immediately posterior to it. The Sylvian fissure separates the opercula of the temporal lobe (inferiorly) from the frontal opercula (anteriorly) and the parietal opercula (posteriorly). It travels posteriorly and superiorly, and terminates approximately one-third of the way along the horizontal length of the parietal lobe. Broca's area is part of the frontal opercula, located within the inferior frontal gyrus, lying above the Sylvian fissure. Wernicke's area is part of the temporal opercula, found immediately behind and below the posterior termination of the Sylvian fissure at the superior temporal gyrus; traditionally, this area is thought to be involved in enabling speech comprehension. The insula is a deep infolding of cortex lying within the Sylvian fissure and is typically obscured from view unless the Sylvian fissure is ‘opened’.

Cortical and subcortical anatomy of the insula

The insula resembles a cortical shield that covers the external capsule of white matter and protects the deeply located basal ganglia. The insular cortex is involved in visceral sensation, regulation of sympathetic cardio­vascular tone, pain processing and motor planning, among other somatosensory functions. Insular gliomas represent a technical challenge for the neurosurgeon due to difficult-to-reach anatomy, relations of highly eloquent cortex and a complex vascular supply. The insular cortex, when exposed, is divided by the oblique insular central sulcus and bounded by the anterior, superior and inferior peri-insular sulci at its anterior, superior and inferior walls, respectively. Anterior to the central sulcus there are three oblique gyri: the anterior, middle and posterior short insular gyri ( Fig. 25.1A ). Posterior to the central sulcus are the anterior and posterior long gyri. The most anteroinferior polar extremity of the insula is the limen insulae, containing the temporal stem (uncinate and inferior fronto-occipital fasciculi) ( Fig. 25.1B ). Deep to the central insula are the extreme capsule, claustrum, external capsule and lentiform nucleus. Posteriorly, geniculate motor fibres within the internal capsule run deep to the posterosuperior extremity of the circular sulcus.

Fig. 25.1, A , Removal of para-insular structures reveals the insular gyrus lying within the Sylvian fissure. Obliquely bisecting the insular surface is the central insular sulcus (white perforated line). Gyral convolutions lying anterior to the central sulcus are the anterior (ASG), middle (MSG) and posterior (PSG) short gyri. These converge inferiorly to form the limen insulae (LI). Lying posterior to the central sulcus are the anterior (ALG) and posterior (PLG) long gyri. B , Lying deep to the insular cortex are critical white matter structures that may be damaged during surgery. The temporal stem consists of association white matter of the uncinate fasciculus (UF; anterior) and inferior fronto-occipital fasciculus (IFOF, posterior); the claustrum (Claust.) lies deep to the dorsal insular aspect.

Vascular supply of the insula

The insular cortex is supplied by perforators given off the M 2 and M 3 segments of the middle cerebral artery. Collateral perforators given off by the prefrontal artery, originating from the superior trunk of M2, supply the anterior short insular gyrus. Perforators from the precentral artery, again originating from the superior trunk, supply the middle short insular gyrus. M2 subsequently continues postero­superiorly along the lateral insular surface as the superior trunk, which branches into the central, anterior parietal, posterior parietal, angular and temporo-occipital arteries. These branches give off perforators supplying the posterior insular gyri. The inferior edge of the insula is supplied by either the temporal branch or the inferior trunk of the middle cerebral artery, which bifurcates into the middle and posterior temporal arteries that give off perforators supplying the cortex.

Surgical resection of insular tumours

The M1 segment gives off lenticulostriate perforators prior to its bifurcation into M2 branches. The lenticulostriate perforators represent the medial limit of resection for insular gliomas. Identification of vascular structures is critical during insular surgery because inadvertent damage may produce ischaemic deficits. Surgery involves careful Sylvian fissure dissection and retraction of the temporal and frontal lobes to expose the insular surface. An alternative approach has been developed to avoid Sylvian fissure opening and dissection of middle cerebral artery branches, involving the use of intraoperative cortical mapping to identify eloquent cortex. Non-dominant insular tumours can be removed under general anaesthesia, with mapping of facial somatic responses. Dominant hemispheric tumours must be removed using awake crani­otomy, with concurrent speech mapping to ensure language preservation. Once language and motor cortical regions are localized, safe cortical ‘windows’ are created to access the insular region in a subpial fashion, preserving the pia–arachnoid layering overlying middle cerebral artery branches. With these factors taken into consideration, insular tumours, particularly low-grade gliomas once thought to be inoperable, can be safely removed with significant improvement in oncosurgical outcomes.

Frontal lobe

The frontal lobe is divided by the precentral sulcus, which runs anterior and parallel to the deep central sulcus and defines the anterior limit of the precentral/motor gyrus. The superior frontal sulcus begins anteriorly, perpendicular to the precentral sulcus, and demarcates the lateral limit of the superior frontal gyrus, which runs adjacent to the interhemispheric fissure. The middle frontal gyrus lies inferior to the superior frontal sulcus and travels parallel to the superior frontal gyrus. The ventral limit of the middle frontal gyrus is demarcated by the inferior frontal sulcus running parallel to the superior frontal sulcus. The most ventral and lateral aspect of the frontal lobe is the inferior frontal gyrus. It is further divided by an ‘M’-shaped sulcal arrangement, from dorsal–ventral and posterior–anterior, into the pars opercularis, pars triangularis and pars orbitalis. The former two contribute to Broca's area, traditionally associated with the expressive aspect of speech.

Parietal lobe

The anterior limit of the parietal lobe is bounded by the central sulcus, with the postcentral gyrus lying immediately behind and running parallel to it. The inferior third of the parietal lobe is bounded by the Sylvian sulcus. An ‘H’-shaped sulcal system further divides the part of the parietal lobe posterior to postcentral gyrus. The anterior and vertical limb of the ‘H’ is formed by the postcentral sulcus, the horizontal limb by the intraparietal sulcus, and the posterior–vertical limb by the parieto-occipital arcus. The superior and inferior parietal lobules lie immediately behind the postcentral gyrus, separated dorsoventrally by the intraparietal sulcus. The inferior parietal lobule contains two important parieto-temporal gyri: the supramarginal (anterior) and angular (posterior) gyri.

Occipital lobe

The parieto-occipital arcus demarcates the anterior and dorsal boundaries of the occipital lobe; the ventral boundary is approximately delineated by the terminations of the horizontally travelling superior and inferior temporal sulci. Two opposing sulci divide the occipital lobe into an approximate wedge shape. The transverse occipital sulcus runs dorsoventrally and posteroanteriorly, where it is met by the lateral occipital sulcus running posteroanteriorly. The demarcation of the occipital lobe is more distinct when viewed from a medial perspective. The cuneus is the region between the parieto-occipital sulcus and the calcarine fissure. The lingual gyrus lies ventral or inferior to the calcarine sulcus.

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