Intracranial region

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CHAPTER 27 Intracranial region

The cranial cavity contains the brain, the intracranial portions of cranial and spinal nerves, blood vessels, meninges and cerebrospinal fluid. Its walls are formed by parts of the frontal, ethmoid, parietal, sphenoid, temporal and occipital bones.

INTERNAL SURFACE OF CRANIAL VAULT

The internal surface of the cranial vault is deeply concave. It includes most of the frontal and parietal bones and the squamous part of the occipital bone, variously united at the coronal, sagittal and lambdoid sutures (Fig. 27.1). With increasing age, these sutures become obliterated by a gradual process that begins on their intracranial surfaces. Inconstant foramina may occur in the parietal bones near the sagittal sulcus and anterior to the lambdoid suture: they admit emissary veins associated with the superior sagittal sinus. The internal surfaces of the frontal and parietal bones are grooved by furrows that house the frontal and parietal branches of the middle meningeal vessels; the grooves contain the openings of minute channels that admit perforating vessels to the haemopoietic marrow within the diploic bone. Impressions for cerebral gyri are less distinct on the vault than they are on the cranial base.

image

Fig. 27.1 Internal surface of the cranial vault.

(From Drake, Vogl and Mitchell 2005.)

The falx cerebri, a dural partition that passes between the two cerebral hemispheres of the brain, is attached anteriorly to a backward projecting anteromedian frontal crest. The crest exhibits a groove that widens as it passes back below the sagittal suture and becomes continuous with the sagittal sulcus which houses the superior sagittal sinus. Irregular depressions, granular foveolae, which become larger and more numerous with age, lie on either side of the sulcus and usually house arachnoid granulations.

CRANIAL FOSSAE (ANTERIOR, MIDDLE, POSTERIOR)

The base of the cranial cavity is divided into three distinct fossae, the anterior, middle and posterior cranial fossae (Fig. 27.2). The floor of the anterior cranial fossa is at the highest level and the floor of the posterior fossa is at the lowest.

Detailed descriptions of the microsurgical anatomy of each region of the cranial base are beyond the scope of this book, and the interested reader is directed in the first instance to Rhoton (2002).

ANTERIOR CRANIAL FOSSA

The anterior cranial fossa is formed at the front and sides by the frontal bone. Its floor is composed of the orbital plate of the frontal bone, the cribriform plate and crista galli of the ethmoid bone, and the lesser wings and anterior part of the body of the sphenoid. Unlike the other cranial fossae, it does not directly communicate with the inferior surface of the cranium.

A perforated plate of bone, the cribriform plate of the ethmoid bone, spreads across the midline between the orbital plates of the frontal bone, and is depressed below them, forming part of the roof of the nasal cavity. Olfactory nerves pass from the nasal mucosa to the olfactory bulb of the brain through numerous small foramina in the cribriform plate. Anteriorly a spur of bone, the crista galli, projects upwards between the cerebral hemispheres. A depression between the crista galli and the crest of the frontal bone is crossed by the fronto-ethmoidal suture. It bears the foramen caecum, which is usually a small blind-ended depression, but which occasionally accommodates a vein draining from the nasal mucosa to the superior sagittal sinus. The anterior ethmoidal nerve enters the cranial cavity where the cribriform plate meets the orbital part of the frontal bone and then passes into the roof of the nose via a small foramen by the side of the crista galli: the nerve grooves the crista galli. The anterior ethmoidal vessels accompany the nerve. The posterior ethmoidal canal, which transmits the posterior ethmoidal nerve and vessels, opens at the posterolateral corner of the cribriform plate and is overhung by the sphenoid bone.

The convex cranial surface of the frontal bone separates the brain from the orbit and bears impressions of cerebral gyri and small grooves for meningeal vessels. Posteriorly, it articulates with the anterior border of the lesser wing of the sphenoid bone which forms the posterior boundary of the anterior cranial fossa. The medial end of the lesser wing constitutes the anterior clinoid process. The lesser wing joins the body of the sphenoid body by two roots which are separated by the optic canal. The anterior root, broad and flat, is continuous with the jugum sphenoidale, while the smaller and thicker posterior root joins the body of the sphenoid bone near the posterior bank of the sulcus chiasmatis. The frontosphenoid and sphenoethmoidal sutures divide the sphenoid from the adjacent bones.

The posterior border of each lesser wing fits the stem of the lateral cerebral sulcus and may be grooved by the sphenoparietal sinus. Above lies the inferior surface of the frontal lobe of the cerebral hemisphere and the anterior perforated substance lies medially. Inferiorly the lesser wing bounds the superior orbital fissure, and completes the orbital roof. Each anterior clinoid process gives attachment to the free margin of the tentorium cerebelli and is grooved medially by the internal carotid artery as it leaves the cavernous sinus. The anterior and middle clinoid processes may be connected by a thin osseous bar, formed by ossification either of the carotico-clinoid ligament or of a dural fold extending between the processes: the resulting carotico-clinoid foramen surrounds the artery.

MIDDLE CRANIAL FOSSA

The middle cranial fossa is deeper and more extensive than the anterior fossa, particularly laterally, where it supports the temporal lobes of the cerebral hemispheres. It is bounded in front by the lesser wings and part of the body of the sphenoid, behind by the superior borders of the petrous part of the temporal bone and the dorsum sellae of the sphenoid, and laterally by the squamous parts of the temporal bone, parietal bone and greater wings of the sphenoid. The region corresponds with the middle part of the cranial base.

The middle cranial fossa communicates with the orbits by the superior orbital fissures, each bounded above by a lesser wing, below by a greater wing, and medially by the body of the sphenoid bone. The fissures are wider medially, and each has a long axis sloping inferomedially and forwards. They are the major gateways into the orbit from the cranial cavity and contain the oculomotor, trochlear and abducens nerves, and the lacrimal, frontal and nasociliary branches of the ophthalmic division of the trigeminal nerve, together with filaments from the internal carotid plexus (sympathetic), the ophthalmic veins, the orbital branch of the middle meningeal artery, and the recurrent branch of the lacrimal artery (see Ch. 39).

Centrally the floor of the fossa is narrower and formed by the body of the sphenoid bone which contains the sphenoidal sinuses (see Ch. 32). The roof of the sinus is deeply concave and houses the pituitary gland (hypophysis): it is therefore termed the pituitary (hypophysial) fossa, also known as the sella turcica because it resembles the shape of a Turkish saddle. The anterior edge of the pituitary fossa is completed laterally by a middle clinoid process, the floor forms the roof of the sphenoidal air sinuses, and the posterior boundary presents a vertical pillar of bone, the dorsum sellae. The superolateral angles of the dorsum are expanded as the posterior clinoid processes. A fold of dura, the diaphragma sella, is attached to the anterior and posterior clinoid processes and roofs over the pituitary fossa. The smooth upper part of the anterior wall of the fossa, the jugum sphenoidale, is bounded behind by the anterior border of the grooved sulcus chiasmatis which leads laterally into the optic canals. Each canal transmits the optic nerve and ophthalmic artery. The optic chiasma usually lies posterosuperior to the sulcus chiasmatis, the tuberculum sellae lies below the sulcus. The cavernous sinus lies lateral to the pituitary fossa. The lateral wall of the body of the sphenoid contains a shallow carotid groove related to the internal carotid artery as it ascends from the carotid canal and runs through the cavernous sinus. Posterolaterally the groove may be deepened by a small projecting lingula.

The greater wing of the sphenoid bone contains three consistent foramina and other small variable foramina. The foramen rotundum, situated just below and behind the medial end of the superior orbital fissure, leads forwards into the pterygopalatine fossa, and contains the maxillary nerve. Behind the foramen rotundum is the foramen ovale which transmits the mandibular nerve: it is occasionally divided into two or three components. Accessory named foramina, the foramen of Vesalius and the cavernous foramen, may occur close to the foramen ovale. The small foramen of Vesalius occurs in some 20% of skulls: it is consistently symmetrical and lies anteromedial to the foramen ovale and lateral to the foramen rotundum and vidian canal. It transmits an emissary vein through which the cavernous sinus and pterygoid plexus communicate. The foramen spinosum lies posterolateral to the foramen ovale and transmits the middle meningeal artery and veins. The vessels groove the floor and lateral wall of the middle cranial fossa. The foramen ovale and foramen spinosum open into the underlying infratemporal fossa.

The foramen lacerum is situated at the posterior end of the carotid groove, posteromedial to the foramen ovale. It is bounded in front by the body and adjoining roots of the pterygoid process and greater wing of the sphenoid bone, posterolaterally by the apex of the petrous part of the temporal bone, and medially by the basilar part of the occipital bone. A small emissary sphenoidal foramen may occur at the root of the greater wing of the sphenoid medial to the foramen lacerum; when present it transmits a vein from the cavernous sinus.

The trigeminal impression, which accommodates the trigeminal ganglion, is situated posterior to the foramen lacerum on the anterior surface of the petrous part of the temporal bone near its apex. Its depth is variable. Posterolateral to the impression is a small, shallow, pit, limited posteriorly by a rounded arcuate eminence (produced by the underlying anterior semicircular canal). Lateral to the impression a narrow groove passes posterolaterally into the hiatus for the greater petrosal nerve, and even further laterally is the hiatus for the lesser petrosal nerve. A smooth trigeminal notch leads into the impression. It lies on the upper border of the petrous temporal, anteromedial to the groove for the superior petrosal sinus; at this point, the trigeminal nerve separates the sinus from bone. At the anterior end of the trigeminal notch is the petrosphenoidal ligament (of Gruber), attached to a minute bony spicule, directed anteromedially. The abducens nerve bends sharply across the upper petrous border, and passes between the ligament and the dorsum sellae anterior to the petrosphenoidal ligament (for a detailed analysis of the course of the abducens nerve in the petroclival region see Ozveren et al 2002).

The anterior surface of the petrous part of the temporal bone is formed by the tegmen tympani, a thin osseous lamina in the roof of the tympanic cavity, which extends anteromedially above the pharyngotympanic tube, anterolateral to the arcuate eminence. The posterior part of the tegmen tympani roofs the mastoid antrum, lateral to the eminence. The superior border of the petrous part of the temporal bone separates the middle and the posterior cranial fossae, and is grooved by the superior petrosal sinus. In young skulls, a petrosquamous suture may be visible at the lateral limit of the tegmen tympani but it is obliterated in adults. The tegmen tympani then turns down as the lateral wall of the osseous portion of the pharyngotympanic tube and its lower border may appear in the squamotympanic fissure. Lateral to the anterior part of the tegmen tympani, the squamous part of the temporal bone is thinned over a small area that coincides with the deepest part of the mandibular fossa.

POSTERIOR CRANIAL FOSSA

The posterior cranial fossa, the largest and deepest of the cranial fossae, contains the cerebellum, pons and medulla oblongata. It is bounded in front by the dorsum sellae, posterior aspects of the body of the sphenoid and the basilar part of occipital bone; behind by the squamous part of the occipital bone; laterally by the petrous and mastoid parts of the temporal bone and by the lateral parts of the occipital bone; and above and behind by the mastoid angles of the parietal bones. The region corresponds extracranially with the posterior part of the cranial base.

The most prominent feature in the floor of the posterior cranial fossa is the foramen magnum in the occipital bone. A sloping surface, the clivus, formed successively by the basilar part of the occipital bone, the posterior part of the body and then the dorsum sellae of the sphenoid bone, lies anterior to the foramen magnum. The clivus is gently concave from side to side. On each side it is separated from the petrous part of the temporal bone by a petro-occipital fissure, which is filled by a thin plate of cartilage and limited behind by the jugular foramen. Its margins are grooved by the inferior petrosal sinus. The spheno-occipital synchondrosis is evident on the clivus of a growing child.

The jugular foramen is a large opening sited at the posterior end of the petro-occipital fissure, above and lateral to the foramen magnum. Its upper border is sharp and irregular, and contains a notch for the glossopharyngeal nerve. The cochlear canaliculus, which contains the perilymphatic ‘duct’, is sited in the deepest part of the notch. The lower border of the jugular foramen is smooth. Posteriorly it is grooved by the sigmoid sinus which continues into the foramen as the internal jugular vein. The accessory, vagus and glossopharyngeal nerves pass through the anterior part of the jugular foramen from behind forwards, and may groove the jugular tubercle as they enter the foramen. They lie between the inferior petrosal sinus (accompanied by a meningeal branch of the ascending pharyngeal artery) and the sigmoid sinus (accompanied by a meningeal branch of the occipital artery).

The hypoglossal (anterior condylar) canal lies medial to and below the lower border of the jugular foramen, at the junction of the basilar and lateral parts of the occipital bone. It transmits the hypoglossal nerve and its recurrent branch together with the meningeal branch of the ascending pharyngeal artery and an emissary vein which links the (intracranial) basilar plexus with the (extracranial) internal jugular vein. When a posterior condylar canal is present behind the occipital condyle, its internal orifice is posterolateral to that of the hypoglossal canal and it contains a sigmoid emissary vein (associated with the occipital veins) and a meningeal branch of the occipital artery. The occipital condyles lie within the anterior aspect of the foramen magnum: their medial aspects are roughened for the attachments of the alar ligaments associated with the atlanto-axial joints.

The posterior surface of the petrous part of the temporal bone forms much of the anterolateral wall of the posterior cranial fossa. It contains the internal acoustic meatus, which lies anterosuperior to the jugular foramen, and transmits the facial and vestibulocochlear nerves, the nervus intermedius, and labyrinthine vessels.

The mastoid part of the temporal bone lies behind the petrous part of the temporal bone in the lateral wall of the posterior cranial fossa. Anteriorly it is grooved by a wide sigmoid sulcus which runs forwards and downwards, then downwards and medially, and finally forwards to the jugular foramen: it contains the sigmoid sinus. Superiorly, where the groove touches the mastoid angle of the parietal bone, it becomes continuous with a groove that transmits the transverse sinus, and then crosses the parietomastoid suture and descends behind the mastoid antrum. A mastoid foramen which transmits an emissary vein from the sigmoid sinus and a meningeal branch of the occipital artery, sometimes large enough to groove the squamous part of the occipital bone, may be sited here. The lowest part of the sigmoid sulcus crosses the occipitomastoid suture and grooves the jugular process of the occipital bone. The right sigmoid sulcus is usually larger than the left.

A thin plate with an irregularly curved margin projects back behind the internal acoustic meatus. It bounds a slit that contains the opening of the vestibular aqueduct (which houses the saccus and ductus endolymphaticus and a small artery and vein). A small subarcuate fossa lined with dura mater lies between the internal acoustic meatus and the aqueductal opening. Near the superior border of the petrous part of the temporal bone the fossa is pierced by a small vein. In infants the fossa is a relatively large blind tunnel under the anterior semicircular canal.

The squamous part of the occipital bone displays a median internal occipital crest. This runs posteriorly from the foramen magnum to an internal occipital protuberance, gives attachment to the falx cerebelli, and may be grooved by the occipital sinus. The internal occipital protuberance is close to the confluence of the sinuses. It is grooved bilaterally by the transverse sinuses which curve laterally with an upward convexity to the mastoid angles of the parietal bones. The groove for the transverse sinus is usually deeper on the right, where it is generally a continuation of the superior sagittal sinus, while on the left it is frequently a continuation of the straight sinus. On both sides the transverse sulcus is continuous with the sigmoid sulcus. Below the transverse sulcus, the internal occipital crest separates two shallow fossae which house the cerebellar hemispheres. The posterior clinoid process and the margins of the grooves for the transverse and superior petrosal sinuses all provide anchorage for the attached margin of the tentorium cerebelli.

MENINGES

Three concentric membranes, the meninges, envelop the brain and spinal cord. They provide support and protection for the delicate tissues they surround. The individual layers, in order from outside to inside, are the dura mater (pachymeninx), arachnoid mater and pia mater. The dura is an opaque, tough, fibrous coat which incompletely divides the cranial cavity into compartments and accommodates the dural venous sinuses. The arachnoid is much thinner than the dura and is mostly translucent. It surrounds the brain loosely, spanning over depressions and concavities. The pia mater is a transparent, microscopically thin, membrane which follows the contours of the brain and is closely adherent to its surface.

The dura is separated from the arachnoid by a narrow subdural space. The arachnoid is separated from the pia by the subarachnoid space, which varies greatly in depth; the larger expanses are termed subarachnoid cisterns. The subarachnoid space contains cerebrospinal fluid, CSF, which is secreted by the choroid plexuses of the cerebroventricular system. CSF circulates within the subarachnoid space and is reabsorbed into the venous system through arachnoid villi and granulations associated with the dural venous sinuses.

Cranial and spinal meninges are continuous through the foramen magnum. The cranial meninges are described in this section and the spinal meninges are described on p. 751).

DURA MATER

Dura mater is thick, dense and fibrous. It is predominantly acellular, and consists mainly of densely packed fascicles of collagen fibres arranged in laminae. The fascicles run in different directions in adjacent laminae, producing a lattice-like appearance which is particularly obvious in the tentorium cerebelli and around the defects or perforations that sometimes occur in the anterior portion of the falx cerebri.

The cranial dura, which lines the cranial cavity, differs from the spinal dura mainly in its relationship to the surrounding bones. It has an inner, or meningeal, layer and an outer, or endosteal, layer. These layers are united except where they separate to enclose the venous sinuses that drain blood from the brain. There is little histological difference between the endosteal and meningeal layers. Both contain fibroblasts, and the endosteal layer also contains osteoblasts. Focal calcification may occur in the falx cerebri.

The dura mater adheres to the internal surfaces of the cranial bones, particularly at the sutures, the cranial base and around the foramen magnum. Fibrous bands pass from the dura into the bones, and it is difficult to remove the dura from the suture lines in young skulls. However, as the suture lines fuse the dura becomes separated from them. It also becomes thicker, less pliable, and more firmly adherent to the inner surface of the skull, particularly that of the calvaria, with increasing age. The endosteal layer of the dura is continuous with the pericranium through the cranial sutures and foramina and with the orbital periosteum through the superior orbital fissure. The meningeal layer provides tubular sheaths for the cranial nerves as they pass out through the cranial foramina, and these sheaths fuse with the epineurium as the nerves emerge from the skull. The dural sheath of the optic nerve is continuous with the ocular sclera. The dura fuses with the adventitia of major vessels, such as the internal carotid and vertebral arteries, at sites where they pierce it to enter the cranial cavity.

The inner aspect of the dura mater is closely applied to the arachnoid mater over the surface of the brain. However the two membranes are physically joined only at sites where either veins pass from the brain into venous sinuses, e.g. the superior sagittal sinus, or where they connect the brain to the dura, e.g. at the anterior pole of the temporal lobe.

Dural partitions

The meningeal layer of the dura is reflected inwards to form four septa, namely the falx cerebri, falx cerebelli, diaphragma sellae and tentorium cerebelli that partially divide the cranial cavity into compartments.

Falx cerebri

The falx cerebri is a strong, crescent-shaped sheet that lies in the sagittal plane and occupies the longitudinal fissure between the two cerebral hemispheres (Fig. 27.3). The crescent is narrow in front, where the falx is fixed to the crista galli, and broad behind, where it blends with the tentorium cerebelli: the straight sinus runs along this line of attachment (Fig. 27.3). The anterior part of the falx is thin and may have a number of irregular perforations. Its convex upper margin is attached to the internal cranial surface on each side of the midline, as far back as the internal occipital protuberance. The superior sagittal sinus runs in a cranial groove within the dura along this margin: the falx is attached to the lips of this groove. The lower edge of the falx is free and concave and contains the inferior sagittal sinus.

Tentorium cerebelli

The shape of the tentorium cerebelli (Fig. 27.3) is reminiscent of a single-poled tent, from which its name is derived. It lies between the cerebellum and the occipital lobes of the cerebral hemispheres and divides the cranial cavity into supratentorial and infratentorial compartments, which contain the forebrain and hindbrain respectively. Its concave anterior edge is free and separated from the dorsum sellae of the sphenoid bone by a large curved hiatus, the tentorial incisure or notch, which is filled by the midbrain and the anterior part of the superior aspect of the cerebellar vermis. The convex outer limit of the tentorium is attached posteriorly to the lips of the transverse sulci of the occipital bone and to the posterior-inferior angles of the parietal bones, where it encloses the transverse sinuses. Laterally, it is attached to the superior borders of the petrous parts of the temporal bones, where it contains the superior petrosal sinuses. On each side, near the apex of the petrous temporal bone, the lower layer of the tentorium is evaginated anterolaterally under the superior petrosal sinus to form a recess between the endosteal and meningeal layers in the middle cranial fossa. The recess contains the roots and ganglion of the trigeminal nerve; the evaginated meningeal layer fuses in front with the anterior part of the ganglion.

The arrangement of the dura mater in the central part of the middle cranial fossa is complex. The tentorium forms a large part of the floor of the middle cranial fossa, and fills much of the gap between the ridges of the petrous temporal bones. On both sides, the rim of the tentorial incisure is attached to the apex of the petrous temporal bone and continues forward as a ridge of dura mater to attach to the anterior clinoid process. This ridge marks the junction of the roof and the lateral part of the cavernous sinus. The periphery of the tentorium cerebelli (attached to the superior border of the petrous temporal bone), crosses under the free border of the tentorial incisure at the apex of the petrous temporal bone, and continues forward to the posterior clinoid processes as a rounded, indefinite ridge of the dura mater. The angular depression between the anterior parts of the peripheral attachment of the tentorium and the free border of the tentorial incisure is part of the roof of the cavernous sinus. It is pierced in front by the oculomotor and behind by the trochlear nerves, which proceed anteroinferiorly into the lateral wall of the cavernous sinus. In the anteromedial part of the middle cranial fossa the dura ascends as the lateral wall of the cavernous sinus, reaches the ridge produced by the anterior continuation of the free border of the tentorium, and runs medially as the roof of the cavernous sinus, where it is pierced by the internal carotid artery. Medially, the roof of the sinus is continuous with the upper layer of the diaphragma sellae. At, or just below, the opening in the diaphragma for the infundibulum and pituitary stalk, the dura, arachnoid and pia mater blend with each other and with the capsule of the pituitary gland. The layers of the meninges cannot be distinguished within the sella turcica, and the subarachnoid space is obliterated.

Dural venous sinuses

Dural venous sinuses form a complex network of venous channels which drain blood from the brain and cranial bones (Fig. 27.4, see Fig. 17.10). They lie between the endosteal and meningeal layers of dura mater, are lined by endothelium, have no valves, and their walls are devoid of muscular tissue. They develop initially as venous plexuses, and most adult sinuses preserve a plexiform arrangement (to a variable degree), rather than being simple vessels with a single lumen. Plexiform arrays of small veins adjoin the sagittal superior and inferior sagittal and straight sinuses and, less frequently, the transverse sinuses, and ridges of ‘spongy’ venous tissue often project into the lumina of the superior sagittal and transverse sinuses (Browder & Kaplan 1976; Kaplan & Browder 1976).

The structure of cranial venous sinuses, their plexiform nature and wide connections with cerebral and cerebellar veins, vary considerably, particularly in earlier years, e.g. in infancy the falx cerebelli may contain large plexiform channels and venous lacunae that augment the occipital sinus. These variations cannot be detailed in a general text but must be established for the individual by angiography when clinical necessity arises. There is experimental evidence that parts of sinuses (and even diploic veins) can be filled by forcible internal carotid injection, from which it has been inferred that arteriovenous shunts may exist (Browder & Kaplan 1976). A connection between the middle meningeal arteries and the superior sagittal sinus has been demonstrated in this way, although the sites of communication are unknown. Dural arteriovenous fistulas are thought to be acquired lesions that form in an area of thrombosis within a sinus. If the sinus remains completely thrombosed, venous drainage from these lesions occurs through cortical veins, or, if the sinus is open, venous drainage is usually into the involved sinus.

The named sinuses are the superior and inferior sagittal, straight, transverse, petrosquamous, sigmoid, occipital, cavernous, intercavernous, superior and inferior petrosal, sphenoparietal, basilar and marginal.

Superior sagittal sinus

The superior sagittal sinus runs in the attached convex margin of the falx cerebri. It grooves the internal surface of the frontal bone, the adjacent margins of the two parietal bones and the squamous part of the occipital bone (Fig. 27.3, Fig. 27.5, see Fig. 17.10). It begins near the crista galli, a few millimetres posterior to the foramen caecum, and receives primary tributaries from cortical veins of the frontal lobes, the ascending frontal veins. The sinus is triangular in cross-section and invaded, in its intermediate third, by variable bands and projections from its dural walls, which may extend as horizontal shelves that divide its lumen into superior and inferior channels. It is narrow anteriorly, and widens gradually to approximately 1 cm diameter as it runs backwards. At its posterior end, the sinus enters the confluence of the sinuses (Fig. 27.4) which is situated to one side (usually the right) of the internal occipital protruberance. At the confluence the superior sagittal sinus usually deviates to become continuous with the right transverse sinus, but it also usually connects with the occipital and contralateral transverse sinuses. The size and degree of communication of the channels meeting at the confluence are highly variable: any sinus involved may be duplicated, narrowed, or widened near the confluence. In more than half of subjects all venous channels that converge towards the occiput interconnect, including the straight and occipital sinuses, but communication between channels may be absent or tenuous.

The superior sagittal sinus receives the superior cerebral veins and communicates by small orifices with irregular venous lacunae which lie near it in the dura mater. There are usually two or three lateral lacunae on each side of the midline, named frontal (small), parietal (large) and occipital (intermediate) lacunae: they tend to become confluent in the elderly, producing a single elongated lacuna on each side. These venous spaces are often so complex as to be almost plexiform. Fine fibrous bands cross the lacunae, and numerous arachnoid granulations project into them (Fig. 27.5, Fig. 27.6). The lacunae drain diploic and meningeal veins. Near its posterior end, the superior sagittal sinus receives veins from the pericranium which pass through parietal foramina.

Inferior sagittal sinus

The inferior sagittal sinus is located in the posterior half or two-thirds of the free margin of the falx cerebri (Fig. 27.3). It increases in size posteriorly, ends in the straight sinus and receives veins from the falx and sometimes from the medial surfaces of the cerebral hemispheres.

Straight sinus

The straight sinus lies in the junction of the falx cerebri with the tentorium cerebelli (Fig. 27.3, see Fig. 17.10). It runs posteroinferiorly as a continuation of the inferior sagittal sinus and drains into the transverse sinus. It is not (or only tenuously) continuous with the superior sagittal sinus. Its tributaries include the great cerebral vein and some superior cerebellar veins. It is triangular in cross-section.

Transverse sinus

The transverse sinuses begin at the internal occipital protuberance (Fig. 27.3, Fig. 27.4). One, usually the right, is directly continuous with the superior sagittal sinus, the other with the straight sinus. On both sides the sinuses run in the attached margin of the tentorium cerebelli, first on the squama of the occipital bone, then on the mastoid angle of the parietal bone. Each follows a gentle anterolateral curve, increasing in size as it does so, to the posterolateral part of the petrous temporal bone. Here it turns down as a sigmoid sinus, which ultimately becomes continuous with the internal jugular vein. Transverse sinuses are triangular in section and usually unequal in size; the one draining the superior sagittal sinus is the larger. They receive the inferior cerebral, inferior cerebellar, diploic and inferior anastomotic veins, and are joined by the superior petrosal sinuses where they continue as sigmoid sinuses.

Occipital sinus

The occipital sinus is the smallest of the sinuses. It lies in the attached margin of the falx cerebelli (Fig. 27.4) and is occasionally paired. It commences near the foramen magnum in several small channels, one joining the end of the sigmoid sinus, and connects with the internal vertebral plexuses. It ends in the confluence of the sinuses.

Cavernous sinus

The cavernous sinuses are two large venous plexuses that lie on either side of the body of the sphenoid bone, extending from the superior orbital fissure to the apex of the petrous temporal bone, with an average length of 2 cm and width of 1 cm. Each sinus contains the cavernous portions of the internal carotid artery, associated with a perivascular sympathetic plexus that can be seen with the naked eye, and several cranial nerves which run forward through the sinus to access the orbit via the superior orbital fissure (Fig. 27.4, Fig. 27.8, Fig. 27.9). Three major venous spaces have been described within the sinus, posterosuperior, anteroinferior, and medial to the cavernous portion of the carotid artery (Harris & Rhoton 1976). The sphenoidal air sinus and pituitary gland are medial relations and the uncus of the temporal lobe is lateral to the sinus. The trigeminal cave is near the inferoposterior part of its lateral wall, and extends posteriorly beyond it to enclose the trigeminal ganglion.

The oculomotor and trochlear nerves and the ophthalmic and maxillary divisions of the trigeminal nerve all lie in the lateral wall of the sinus. They project into the lumen and are usually covered medially by little more than endothelium. The abducens nerve pierces the dura close to the upper border of the apex of the petrous part of the temporal bone and enters the cavernous sinus by passing below the petrosphenoid ligament within a dural tunnel (Dorello’s canal). The abducens lies on the lateral side of the internal carotid artery, medial to the ophthalmic nerve, and below and medial to the nasociliary nerve. Numerous branches from the cavernous portion of the internal carotid artery, especially from the meningohypophysial and inferolateral trunks, supply the cavernous portions of all of the nerves that pass through the sinus. The preservation of these vessels during cavernous sinus surgery is important in preventing or minimizing postoperative cranial nerve deficits. (For more detailed descriptions of these branches, including their main variations, see Tran-Dinh 1987; Krisht et al 1994; Reisch et al 1996; Tekdemir et al 1998). Propulsion of blood in the cavernous sinus is partly due to pulsation of the internal carotid artery, but it is also influenced by gravity, and hence by the position of the head.

Tributaries of the cavernous sinus are the superior ophthalmic vein, inferior ophthalmic vein (either a branch or the whole vessel), superficial middle cerebral vein, inferior cerebral veins and sphenoparietal sinus. Less frequently, the central retinal vein and frontal tributary of the middle meningeal vein drain into it. The cavernous sinus drains to the transverse sinus via the superior petrosal sinus; to the internal jugular vein via the inferior petrosal sinus and a plexus of veins associated with the internal carotid artery; to the pterygoid plexus by veins traversing the emissary sphenoidal foramen, foramen ovale and foramen lacerum; and to the facial vein via the superior ophthalmic vein.

For more detailed descriptions of the microsurgical anatomy of the cavernous sinus, see Umansky et al 1994; Seoane et al 1998; Yasuda et al 2004.

Caroticocavernous sinus fistula and cavernous sinus thrombosis

Direct communication between the intracavernous portion of the internal carotid artery and the cavernous sinus, creating a caroticocavernous sinus fistula (CCF), occurs occasionally, either as a result of severe head trauma or degenerative or aneurysmal vessel disease. The classic signs are ptosis, proptosis (which may be pulsatile), chemosis, eyelid edema, peri-orbital edema and extra-ocular dysmotility caused by combinations of third, fourth and sixth cranial nerve palsies. Hypo- or hyperesthesia of the ophthalmic and maxillary divisions of the fifth cranial nerve and a decreased corneal reflex may also be detected. There may be evidence of dilated, tortuous retinal veins and papilloedema. These changes can cause permanent blindness. CCFs are most commonly treated by passing a catheter up the carotid into the fistula, and then occluding it with dilatable balloons or flexible metal coils. Any spreading infection involving the upper nasal cavities, paranasal sinuses, cheek (especially near the medial canthus), upper lip, anterior nares or even an upper incisor or canine tooth, may very rarely lead to septic thrombosis of the cavernous sinuses: infected thrombi pass from the facial vein or pterygoid venous complex into the sinus via either ophthalmic veins or emissary veins that enter the cranial cavity through the foramen ovale. This is a critical medical emergency with a high risk of disseminated cerebritis and cerebral venous thrombosis.

Intercavernous sinuses

The two cavernous sinuses are connected by anterior and posterior intercavernous sinuses and the basilar plexus (Fig. 27.4, Fig. 27.8). The intercavernous sinuses lie in the anterior and posterior attached borders of the diaphragma sellae and they thus form a complete circular venous sinus. All connections are valveless and the direction of flow in them is reversible. Small irregular sinuses inferior to the pituitary gland drain into the intercavernous sinuses. The inferior intercavernous sinuses are plexiform in nature and important in a surgical transnasal approach to the pituitary gland.

Superior petrosal sinus

This small narrow sinus drains the cavernous sinus into the transverse sinus on either side (Fig. 27.4, Fig. 27.8). It leaves the posterosuperior part of the cavernous sinus and runs posterolaterally in the attached margin of the tentorium cerebelli. It then crosses above the trigeminal nerve to lie in a groove on the superior border of the petrous part of the temporal bone and ends by joining a transverse sinus at the point where this curves down to become the sigmoid sinus. The superior petrosal sinus receives cerebellar, inferior cerebral and tympanic veins, and connects with the inferior petrosal sinus and the basilar plexus.

Sphenoparietal sinus

Understanding the venous anatomy related to the lesser wing of the sphenoid is of clinical importance in the diagnosis, classification, and treatment of dural arteriovenous fistulas in this region. The classic description of the sphenoparietal sinus is that it is a dural venous channel under the lesser wing of the sphenoid bone, lying near its posterior edge (Fig. 27.4). It curves medially to open into the anterior part of the cavernous sinus and receives small veins from the adjacent dura mater and sometimes the frontal ramus of the middle meningeal vein. It may also receive connecting rami, in its middle course, from the superficial middle cerebral vein, and veins from the temporal lobe and the anterior temporal diploic vein. When these connections are well developed, the sphenoparietal sinus is a large channel. It has recently been suggested that the term sphenoparietal sinus should be abandoned on the basis that it is not an anatomical entity, but an artificial combination of two independent meningeal vessels, namely the parietal portion of the anterior branch of the middle meningeal veins and the sinus of the lesser wing of the sphenoid (see Ruiz et al 2004).

Basilar sinus and plexus

The basilar sinus and plexus consist of interconnecting channels between layers of dura mater on the clivus (Fig. 27.4, Fig. 27.8). The basilar venous plexus interconnects the inferior petrosal sinuses and joins the internal vertebral venous plexus. It also usually connects with the cavernous and superior petrosal sinuses at its anterior end.

Arterial supply and venous drainage of the cranial dura mater

Despite their names, the cranial meningeal arteries are predominantly periosteal (Fig. 27.10A). Their main targets are bone and haemopoietic marrow, and only very fine arterial branches are distributed to the cranial dura mater per se.

The smaller branches of the meningeal vessels lie mainly in the endosteal layer of dura. In the anterior cranial fossa, the dura is supplied by the anterior meningeal branches of the anterior and posterior ethmoidal and internal carotid arteries and a branch of the middle meningeal artery. In the middle cranial fossa, it is supplied by the middle and accessory meningeal branches of the maxillary artery, a branch of the ascending pharyngeal artery (entering via the foramen lacerum), branches of the internal carotid and a recurrent branch of the lacrimal artery. In the posterior fossa, the dura is supplied by the meningeal branches of the occipital artery (one enters the skull by the jugular foramen and another by the mastoid foramen), the posterior meningeal branches of the vertebral artery and occasional small branches of the ascending pharyngeal artery, which enter by the jugular foramen and hypoglossal canal.

Middle meningeal artery

The middle meningeal artery is the largest of the meningeal arteries. It arises from the first part of the maxillary artery and passes between the roots of the auriculotemporal nerve. It may lie lateral to tensor veli palatini, then enters the cranial cavity through the foramen spinosum and runs in an anterolateral groove on the squamous part of the temporal bone, dividing into frontal and parietal branches. The larger frontal (anterior) branch crosses the greater wing of the sphenoid and enters a groove or canal in the sphenoidal angle of the parietal bone (the sphenoparietal canal). It divides into branches between the dura mater and cranium; some branches ascend to the vertex, others to the occipital region. One ascending branch grooves the parietal bone approximately 15 mm behind the coronal suture, and corresponds approximately to the precentral sulcus (Fig. 27.7). The parietal (posterior) branch curves back on the squamous temporal bone, reaches the lower border of the parietal bone anterior to its mastoid angle and divides to supply the posterior parts of the dura mater and cranium. These branches anastomose with their fellows and with the anterior and posterior meningeal arteries.

Ganglionic branches supply the trigeminal ganglion and associated roots. The petrosal branch enters the hiatus for the greater petrosal nerve, supplies the facial nerve, geniculate ganglion and tympanic cavity, and anastomoses with the stylomastoid artery. The superior tympanic artery runs in the canal for tensor tympani and supplies the muscle and the mucosa that lines the canal. Temporal branches traverse minute foramina in the greater wing of the sphenoid and anastomose with deep temporal arteries. An anastomotic branch enters the orbit laterally in the superior orbital fissure, and anastomoses with a recurrent branch of the lacrimal artery: enlargement of this anastomosis is believed to account for the occasional origin of the lacrimal artery from the middle meningeal artery.

Middle meningeal vein (sinus)

The frontal (anterior) branch of the middle meningeal vein crosses the floor of the middle cranial fossa, from either foramen ovale or foramen spinosum, to the pterion, usually in the form of two parallel channels that accompany the middle meningeal artery. The vein subsequently passes cranially along the anterior margin of the parietal squama to empty into the venous lakes of the superior sagittal sinus. As they course under the most lateral aspect of the lesser sphenoid wing, the anterior branches of the middle meningeal vessels are contained for a short distance within a bony canal, the sphenoparietal canal (of Trolard), which they leave to enter a groove on the internal surface of the parietal squama. The veins lie closer to the bone than the artery, and sometimes occupy separate grooves: they are particularly liable to tear in cranial fractures. Before entering the sphenoparietal canal, the anterior branch of the middle meningeal vein usually connects with the sinus of the lesser sphenoid wing. The latter is connected medially with the anterior and superior aspect of the cavernous sinus by a channel that crosses over the superior ophthalmic vein to reach the cavernous sinus.

The parietal (posterior) trunk of the middle meningeal vein may traverse the foramen spinosum to end in the pterygoid venous plexus. The frontal trunk may also reach this plexus via the foramen ovale, or it may end in the sphenoparietal or cavernous sinus (Fig. 27.4). The middle meningeal vein receives meningeal tributaries and small inferior cerebral veins, and connects with the diploic and superficial middle cerebral veins. It frequently bears arachnoid granulations.

Diploic veins

The diploic veins are large, thin-walled vessels that occupy channels in the diploë of the cranial bones (Fig. 27.10B). Four main trunks are usually described; these are the frontal, anterior and posterior temporal, and occipital diploic veins. The frontal opens into the supraorbital vein and the superior sagittal sinus; the anterior temporal is mainly confined to the frontal bone, and opens into the sphenoparietal sinus, and one of the deep temporal veins through an aperture in the great wing of the sphenoid; the posterior temporal is situated in the parietal bone, and empties into the transverse sinus either through an opening at the mastoid angle of the parietal bone or through the mastoid foramen; and the occipital, the largest of the four, is confined to the occipital bone, and may open externally into the occipital vein, or internally into either the transverse sinus or the confluence of the sinuses.

Emissary veins

Emissary veins traverse cranial apertures and make connections between intracranial venous sinuses and extracranial veins. Some are relatively constant, others may be absent. These connections are of clinical significance in determining the spread of infection from extracranial foci to venous sinuses, for example, the spread of infection from the mastoid to the venous sinuses or from the paranasal sinuses to the cavernous sinus.

The following emissary veins have been recognized. A mastoid emissary vein in the mastoid foramen connects the sigmoid sinus with the posterior auricular or occipital veins. A parietal emissary vein in the parietal foramen connects the superior sagittal sinus with the veins of the scalp (these veins are usually minute and do not appear to connect with veins of the scalp in corrosion casts). The venous plexus of the hypoglossal canal, which is occasionally a single vein, connects the sigmoid sinus and the internal jugular vein. A (posterior) condylar emissary vein connects the sigmoid sinus and veins in the suboccipital triangle via the (posterior) condylar canal. A plexus of emissary veins (venous plexus of foramen ovale) connects the cavernous sinus to the pterygoid plexus via the foramen ovale. Two or three small veins which traverse the foramen lacerum and connect the cavernous sinus and the pharyngeal veins and pterygoid plexus. A vein in the emissary sphenoidal foramen (of Vesalius) connects the cavernous sinus with the pharyngeal veins and pterygoid plexus. The internal carotid venous plexus, which passes through the carotid canal, connects the cavernous sinus and the internal jugular vein. The petrosquamous sinus connects the transverse sinus with the external jugular vein. A vein may traverse the foramen caecum (which is patent in about 1% of adult skulls) and connect nasal veins with the superior sagittal sinus. An occipital emissary vein usually connects the confluence of sinuses with the occipital vein through the occipital protuberance, and also receives the occipital diploic vein. The occipital sinus connects with variably developed veins around the foramen magnum (so-called marginal sinuses) and thus with the vertebral venous plexuses; this pathway provides an alternative venous drainage when the jugular vein is blocked or tied. The ophthalmic veins are potentially emissary, because they connect intracranial to extracranial veins.

Innervation of the cranial dura mater

The innervation of the cranial dura mater is derived mainly from the three divisions of the trigeminal nerve, the second and third cervical spinal nerves, and the cervical sympathetic trunk (Fig. 27.11). Less well-established meningeal branches have been described arising from the vagus and hypoglossal nerves and possibly from the facial and glossopharyngeal nerves.

In the anterior cranial fossa, the dura is innervated by meningeal branches of the anterior and posterior ethmoidal nerves and anterior filaments of the meningeal rami of the maxillary (nervus meningeus medius) and mandibular (nervus spinosus) divisions of the trigeminal nerve. Nervi meningeus medius and spinosus are, however, largely distributed to the dura of the middle cranial fossa, which also receives filaments from the trigeminal ganglion. The nervus spinosus re-enters the cranium through the foramen spinosum with the middle meningeal artery, and divides into anterior and posterior branches which accompany the main divisions of the artery and supply the dura mater in the middle cranial fossa and, to a lesser extent, the anterior fossa and calvarium. The anterior branch communicates with the meningeal branch of the maxillary nerve; the posterior branch also supplies the mucous lining of the mastoid air cells. The nervus spinosus contains sympathetic postganglionic fibres from the middle meningeal plexus. The nervus tentorii, a recurrent branch of the intracranial portion of the ophthalmic division of the trigeminal supplies the supratentorial falx cerebri and the tentorium cerebelli. Intraoperative mechanical stimulation of the falx may trigger the trigeminocardiac reflex (Bauer et al 2005). The dura in the posterior cranial fossa is innervated by ascending meningeal branches of the upper cervical nerves which enter through the anterior part of the foramen magnum (second and third cervical nerves) and through the hypoglossal canal and jugular foramen (first and second cervical nerves).

Meningeal branches from the vagus and hypoglossal nerves have been described. Those from the vagus apparently start from the superior vagal ganglion and are distributed to the dura mater in the posterior cranial fossa. Those from the hypoglossal leave the nerve in its canal and supply the diploë of the occipital bone, the dural walls of the occipital and inferior petrosal sinuses, and much of the floor and anterior wall of the posterior cranial fossa. These meningeal rami may not contain vagal or hypoglossal fibres but ascending, mixed sensory and sympathetic fibres from the upper cervical nerves and superior cervical sympathetic ganglion. All meningeal nerves contain a postganglionic sympathetic component, either from the superior cervical sympathetic ganglion or by communication with its perivascular intracranial extensions. The role of the autonomic nerve supply of the cranial dura mater is uncertain.

Sensory nerve endings are restricted to the dura mater and cerebral blood vessels, and are not found in either the brain itself, or in the arachnoid or pia mater. Stimulation of these nerve endings causes pain and is the basis of certain forms of headache.

Arachnoid and pia mater

The arachnoid mater and the pia mater together are sometimes referred to as the leptomeninges. They are separated by the subarachnoid space and joined by trabeculae. They are composed of cells that share a common embryological origin from the mesenchyme that surrounds the developing nervous system. The cells are flattened or cuboidal and each has an oval nucleus, usually with a single small but prominent nucleolus. The outer layer of the arachnoid, the dura–arachnoid interface, is formed from five or six layers of cells joined by numerous desmosomes and tight junctions. This layer forms a barrier that normally prevents permeation of CSF through the arachnoid into the subdural space. The central portion of the arachnoid is closely apposed to the outer layer, and is formed from tightly packed polygonal cells joined by desmosomes and gap junctions. The cells are more loosely packed in the inner layer of the arachnoid, where they intermingle with bundles of collagen continuous with the trabeculae that cross the subarachnoid space. The leptomeningeal cells are not surrounded by basement membrane, except where they are in contact with collagen in the inner layers of the arachnoid and on the deep aspects of the pia mater.

The anatomical relationships of the arachnoid and pia differ to some extent in the cerebral and spinal regions. The cerebral part of the arachnoid mater invests the brain loosely. It does not enter the sulci or fissures, other than the great longitudinal fissure between the cerebral hemispheres, and it coats the superior surface of the pituitary fossa. It is thicker on the basal aspect of the brain and is also slightly opaque where it extends between the temporal lobes and the front of the pons, and produces a large subarachnoid cistern between the arachnoid and underlying pia mater. The arachnoid is easily separated from the dura over the surface of the brain, but adherent to the adventitia of the internal carotid and the vertebral arteries where they enter the subarachnoid space. It is reflected onto the surface of blood vessels in the subarachnoid space and is eventually continuous with the pia mater. In the young, the arachnoid on the upper surface of the brain is transparent, but with age it may become white and opaque, particularly near the midline.

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