Chapter 7 THE MENINGES
Chapter 7 THE MENINGES
The Meninges
D.E. Haines
107
108 Regional Neurobiology
Developing
vertebra Transverse
sinus
Notochord
Third ventricle
B
Cerebellum
Neural tube Primitive meninges Cerebral
aqueduct
Neural crest Tentorium
cerebelli
Cistern
Vertebra Mesoderm
Fourth ventricle
Subarachnoid space
C
Neural tube Endomeninx
Ectomeninx Intervertebral foramen
Mantle layer (future arachnoid
(future dura) and posterior root
Marginal layer and pia) ganglion
Posterior root
Denticulate ligament
Spinal nerve
Vertebrae
E Coccyx
Fig. 7.1 Development of the meninges. After the neural tube closes (A and B),
cells from the neural crest and mesoderm (C, arrows) migrate to surround the
Fig. 7.2 The relation of the meninges to the brain and spinal cord and to their
neural tube and form the primordia of the dura and of the arachnoid and pia (D).
surrounding bony structures. The dura is represented in blue, the arachnoid in
A dermal sinus (E) is a malformation in which there is a channel from the skin
red.
into the meninges.
OVERVIEW OF THE MENINGES by the epidural space (Fig. 7.2). Around the brain the inner por-
In general, the meninges consist of fibroblasts and varying amounts tions of the dura give rise to infoldings or septa, such as the falx
of extracellular connective tissue fibrils. The fibroblasts of each cerebri and tentorium cerebelli (Fig. 7.2), which separate brain
meningeal layer are modified to serve a particular function. regions from each other. Major venous sinuses are found at the
The human meninges are composed of the dura mater, arach- points where these septa originate. Spinal and cranial nerves, as
noid mater, and pia mater (Figs. 7.2 and 7.3). The outermost por- they enter or exit the CNS, must pass through a cuff of the dura
tion, the dura mater, also called the pachymeninx, is adherent to that is continuous with the connective tissue of the peripheral
the inner surface of the skull but is separated from the vertebrae nerve. Blood vessels traverse the dura in similar fashion. Rostrally,
The Meninges 109
Skull
Vessel Periosteal
dura
Dura
mater
Meningeal
dura
Dural
border
cells
Arachnoid
barrier
cells
Basement
membrane
Subarachnoid Arachnoid Arachnoid
space (SAS) trabeculae mater
in SAS
Vessel
Pia mater
Basement
Brain membrane
Collagen
Fig. 7.3 The structure of the meninges. Layers of the dura are shown in shades of gray, the arachnoid in
shades of pink, and the pia in green.
the dura sac is attached to the rim of the foramen magnum. Cau- cell portions. There is no distinct border between periosteal and
dally the sac ends at about the level of the second sacral vertebrae meningeal portions of the dura (Fig. 7.3). Fibroblasts of the peri-
and is attached to the coccyx by the filum terminale externum osteal dura are larger and slightly less elongated than other dural
(or dural part of the filum terminale) (Fig. 7.2). cells. This portion of the dura is adherent to the inner surface
The inner two layers of the meninges, the arachnoid mater of the skull, and its attachment is particularly tenacious along
and the pia mater (Figs. 7.2 and 7.3), are collectively known suture lines and in the cranial base. In contrast, the fibroblasts
as the leptomeninges. This term is also commonly used in of the meningeal dura are more flattened and elongated, their
clinical medicine (as in leptomeningeal cysts and leptomenin- nuclei are smaller, and their cytoplasm may be darker than
gitis). Meningeal infections are frequently sequestered in the that of periosteal cells. Although cell junctions are rarely seen
subarachnoid space; hence they are within the leptomeninges. between dural fibroblasts, the large amounts of interlacing col-
The arachnoid is a thin cellular layer that is attached to the lagen in periosteal and meningeal portions of the dura give these
overlying dura but, with the exception of the arachnoid tra- layers of the meninges great strength.
beculae, is separated from the pia mater by the subarachnoid
space. The arachnoid around the brain is directly continuous Dural Border Cell Layer
with the arachnoid lining the inner surface of the spinal dura The innermost part of the dura is composed of flattened fibro-
(Fig. 7.2). Consequently, the spinal and cerebral subarachnoid blasts that have sinuous processes. Collectively, these cells form
spaces are also directly continuous with each other at the fora- the dural border cell layer (Fig. 7.3). The extracellular spaces
men magnum. The subarachnoid space contains cerebrospi- between the flattened cell processes of dural border cells con-
nal fluid (CSF) and vessels and is bridged by fibroblasts of tain an amorphous substance but no collagen or elastic fibers.
various sizes and shapes that collectively form the arachnoid Cell junctions (desmosomes, gap junctions) are occasionally
trabeculae. The arachnoid is avascular and does not contain seen between dural border cells and cells of the underlying
nerve fibers. arachnoid.
The pia mater is located on the surface of the brain and spinal Because of its loose arrangement, enlarged extracellular
cord and closely follows all their various grooves and elevations spaces, and lack of extracellular connective tissue fibrils, the
(Figs. 7.2 and 7.3). Around the spinal cord, the pia mater con- dural border cell layer constitutes a plane of structural weak-
tributes to the formation of the denticulate ligaments and the ness at the dura-arachnoid junction. This layer is externally
filum terminale internum (or pial part of the filum terminale) continuous with the meningeal dura and internally continuous
(Fig. 7.2). with the arachnoid. Consequently, bleeding into this area of
the meninges will likely disrupt and dissect open the dural
DURA MATER border cell layer rather than invade the overlying dura or the
Periosteal and Meningeal Dura underlying arachnoid. In the normal (and healthy) human,
The dura mater (pachymeninx) is composed of elongated fibro- there is not a naturally occurring, or preexisting, space at the
blasts and copious amounts of collagen fibrils (Fig. 7.3). This dura-arachnoid interface (Fig. 7.3). A space may be created at
membrane contains blood vessels and nerves and is generally this interface by, for example, trauma, bleeding from traversing
divided into outer (periosteal), inner (meningeal), and border veins, or a pathologic process.
110 Regional Neurobiology
Falx cerebri
Inferior sagittal
sinus
Frontal sinus
Great
Crista galli cerebral Straight sinus
vein
Confluence
of sinuses
Falx cerebelli
Sphenoidal sinus
Occipital sinus
Diaphragma sellae
and sella turcica
Fig. 7.4 Midsagittal view of the skull showing the dural infoldings (reflections) and venous sinuses associ-
ated with each.
Blood Supply through the intervertebral foramina and are distributed to the
The arterial supply to the dura of the anterior cranial fossa origi- spinal dura and to some adjacent structures.
nates from the cavernous portion of the internal carotid, the
ethmoidal arteries (via the ethmoidal foramina), and branches of Dural Infoldings and Sinuses
the ascending pharyngeal artery (via the foramen lacerum). The The periosteal dura lines the inner surface of the skull and func-
middle meningeal artery serves the dura of the middle cranial tions as its periosteum. The meningeal dura is continuous with
fossa and may be compromised by skull fractures of the parietal the periosteal dura but draws away from it at specific locations
bone or the squamous portion of the temporal bone, potentially to form the dural infoldings (or reflections). The largest of these
resulting in an epidural hematoma. It is a branch of the maxillary is the falx cerebri (Figs. 7.4 and 7.5A). It is attached to the crista
artery and enters the skull through the foramen spinosum. The galli rostrally, to the midline of the inner surface of the skull,
accessory meningeal artery (via the foramen ovale) and small and to the surface of the tentorium cerebelli caudally. The falx
branches from the lacrimal artery (via the superior orbital fis- cerebri separates the right hemisphere from the left. The supe-
sure) also serve the dura of the middle fossa. The dura of the rior sagittal sinus is found where the falx cerebri attaches to the
posterior fossa is served by small meningeal branches of ascend- skull, the straight sinus where it fuses with the tentorium cer-
ing pharyngeal and occipital arteries and by minute branches of ebelli, and the inferior sagittal sinus at its free edge (Fig. 7.4).
the vertebral arteries. Many large superficial veins located on the surface of the cere-
The spinal dura is served by branches of major arteries (such bral hemispheres empty into the superior sagittal sinus (see Fig.
as vertebral, intercostal, and lumbosacral) that are located close 7.13).
to the vertebral column. These small meningeal arteries enter the The tentorium cerebelli is the second largest of the dural infold-
vertebral canal via the intervertebral foramina to serve the dura ings (Figs. 7.4, 7.5B, C, and 7.6). It attaches rostrally to the clinoid
and adjacent structures. processes, rostrolaterally to the petrous portion of the temporal
bone (location of the superior petrosal sinus), and caudolaterally
Nerve Supply to the inner surface of the occipital bone and a small part of the
The nerve supply to the dura of the anterior and middle fossae parietal bone (location of the transverse sinus) (Figs. 7.4, 7.5B,
is from branches of the trigeminal nerve. Ethmoidal nerves and C, and 7.6). The tent shape of the tentorium divides the cranial
branches of the maxillary and mandibular nerves innervate the cavity into supratentorial (above the tentorium) and infratentorial
dura of the anterior fossa; the dura of the middle fossa is served (below the tentorium) compartments (Figs. 7.5B and 7. 6). The
mainly by branches from the maxillary and mandibular nerves. supratentorial compartment is divided into right and left halves
The dura of the posterior fossa receives sensory branches from by the falx cerebri (Fig. 7.5A, B). The sweeping edges of the right
dorsal roots of C1 to C3 and may have some innervation from and left tentoria, as they arch from the clinoid processes to join at
the vagus nerve. The tentorial nerve, a branch of the ophthalmic the straight sinus, form the tentorial notch (Fig. 7.6). The occipital
nerve, courses caudally to serve the tentorium cerebelli. Auto- lobe is above the tentorium, the cerebellum is below it, and the
nomic fibers to the vessels of the dura originate from the superior midbrain passes through the tentorial notch.
cervical ganglia and simply follow the progressive branching pat- Located below the tentorium cerebelli on the midline of the
terns of the vessels on which they lie. occipital bone is the falx cerebelli (Fig. 7.4). This small dural
Nerves to the spinal dura originate as recurrent branches of infolding extends into the space found between the cerebellar
the spinal nerve located at that level. These delicate strands pass hemispheres and usually contains a small occipital sinus.
The Meninges 111
Falx cerebri
Hemisphere in right
supratentorial
compartment Hemisphere in left
supratentorial
compartment
Falx cerebri
Choroid plexus
in atrium
Tentorium
Cerebellum in cerebelli
infratentorial
compartment
Choroid plexus
Hemisphere in in atrium
supratentorial
compartment
Tentorium
cerebelli
Cerebellum in
infratentorial
compartment
Fig. 7.5 Axial (A), coronal (B), and sagittal (C) T1-weighted magnetic resonance images showing the
relationships of the falx cerebri (A, B) and the tentorium cerebelli (B, C). Note the positions of the right
and left supratentorial compartments and the infratentorial compartment in relation to these large dural
reflections in all three planes.
The smallest of the dural infoldings, the diaphragma sellae sinus. This tear may allow venous blood to enter the subarach-
(Figs. 7.4 and 7.6), forms the roof of the hypophyseal fossa and noid space or may create a hematoma within the dural border
encircles the stalk of the pituitary. The cavernous sinuses are cell layer at the dura-arachnoid interface, a subdural hematoma
found on either side of the sella turcica, and the anterior and pos- (see Fig. 7.13).
terior intercavernous sinuses are found in their respective edges
of the diaphragma sellae. Compartments and Herniation Syndromes
It is emphasized that venous sinuses are endothelium-lined The interior of the cranial cavity is divided into a supratento-
spaces that communicate with each other. In addition, large veins rial compartment located superior to the tentorium cerebelli and
from the surface of the brain empty into the venous sinuses. As consisting of right and left halves (separated by the falx cerebri)
they enter the sinus, these veins are attached to a cuff of dura. and a single infratentorial compartment located inferior to the
Consequently, a blow to the head (or a minor bump to the head tentorium cerebelli (Fig. 7.5). The concept of supratentorial and
in an aged person) may cause the brain to shift just enough in the infratentorial compartments, with an understanding of their con-
subarachnoid space to tear a vein at the point where it enters the tents and relationships, is an essential element in the diagnosis
112 Regional Neurobiology
Diaphragma sellae
Crista galli
Clinoid processes:
Anterior
Posterior
Transverse sinus
Jugular foramen
Fig. 7.6 View of the cranial base from the dorsal aspect showing the tentorium cerebelli (and its associ-
ated sinuses) and the diaphragma sellae. Also indicated are the positions of grooves formed by some of the
major sinuses. The red-shaded area indicates the position of the tentorial incisura (tentorial notch), which
is the space continuation between the supratentorial compartments and the infratentorial compartment.
of what are commonly called herniation syndromes. In general, Cranial Versus Spinal Dura
a herniation syndrome occurs when there is an intracranial event At the margin of the foramen magnum, the periosteal dura essen-
(hemorrhage, rapid tumor growth, traumatic brain injury) that tially stops, but the meningeal dura continues caudally in the ver-
causes an increase in intracranial pressure, forcing the compara- tebral canal to eventually attach to the inner aspect of the coccyx
tively gelatinous brain over the edge of a dural reflection. These as the filum terminale externum (dural part of the filum ter-
syndromes are considered in more detail in later chapters. minale or coccygeal ligament) (Fig. 7.2). The spinal dural sac is
The following are examples of herniation syndromes related to anchored rostrally at the edge of the foramen magnum, caudally
the supratentorial compartments. A lesion in one cerebral hemi- to the coccyx by the filum terminale externum, and is separated
sphere may expand toward the midline, deform the falx cerebri, from the adjacent vertebrae by an epidural space that contains
and force the cingulate gyrus under the edge of the falx into the venous channels, some lymphatics, and fat deposits. There are
opposite hemisphere; this is a subfalcine or cingulate herniation. no dural infoldings around the cord; consequently, there are no
In this example, the deficits may reflect occlusion of the adjacent venous sinuses in the spinal dura.
anterior cerebral artery. Central (or transtentorial) herniation
is the situation in which the diencephalon is forced downward ARACHNOID MATER
through the tentorial incisure or notch. This is a neurologic emer- The arachnoid mater is located internal to the dural border cell
gency, and in about 90% of patients, there is serious disability or layer and is regarded as having two parts (Fig. 7.3). The portion
death. Uncal herniation is the case when a rapidly expanding of the arachnoid directly apposed to the dural border cells is the
lesion, usually a hematoma, forces the uncus, a medial structure arachnoid barrier cell layer, and the spindly cells that traverse
of the temporal lobe, over the edge of the tentorium cerebelli the subarachnoid space constitute the arachnoid trabeculae.
with resultant damage to the midbrain. The most common defi- The subarachnoid space is located between the arachnoid bar-
cits are (1) a decreased level of consciousness, (2) dilation of the rier cell layer and the pial cells on the surface of the brain or
pupil and a loss of most eye movement reflecting damage to the spinal cord. This space contains CSF, many superficial vessels,
ipsilateral oculomotor nerve, and (3) a contralateral hemiplegia and the roots of cranial and spinal nerves as they enter or exit the
reflecting damage to the descending corticospinal fibers. How- nervous system. Enlarged regions of the subarachnoid space are
ever, this early stage is likely to be followed by serious complica- called subarachnoid cisterns.
tions or death.
Examples of herniation syndromes related to the infratentorial Arachnoid Barrier Cell Layer
compartment include upward cerebellar herniation and tonsillar Fibroblasts of this layer are more plump than the flattened cells
herniation. In upward cerebellar herniation, a mass or pressure of the dura (Fig. 7.3). The arachnoid barrier cell layer is tenuously
increase in the posterior fossa may force the cerebellum upward attached to the dural border cell layer by occasional cell junc-
through the tentorial incisura, inflicting damage to the midbrain. tions. In contrast, arachnoid barrier cells have closely apposed
In tonsillar herniation, the tonsils of the cerebellum are forced cell membranes and are joined to each other by numerous tight
downward into and possibly through the foramen magnum. The (occluding) junctions—hence the “barrier” characteristic of this
resulting pressure on the medulla may damage respiratory cen- layer. This close apposition of cell membranes excludes any sig-
ters and result in sudden death. All of the herniation syndromes nificant extracellular space; consequently, no collagen is found
are potentially serious, and all measures should be taken to avoid in this layer of the meninges. The tight junctions between these
their occurrence or to treat their consequences. arachnoid cells not only serve as a barrier against the movement
The Meninges 113
Skull
Venous sinus
Endothelium
Periosteal dura
Meningeal
dura
Dural border
cells
Arachnoid
barrier
cells Meningeal
Pia mater dura
Brain
Fig. 7.7 Structure of the arachnoid villi. Note the continuity of the cell layers of the villus with those of
the meninges. Cerebrospinal fluid (arrows) passes from the subarachnoid space into the villus and then
into the venous sinus.
of fluids but also impart strength to the membrane. A basement fluid milieu of the subarachnoid space by the numerous delicate
membrane (basal lamina) is found on the surface of the barrier strands of the arachnoid trabeculae. This is possible because the
cell layer that faces the subarachnoid space. brain loses about 97% of its weight when it is suspended in CSF.
For example, a brain that weighs about 1400 g in air will weigh
Arachnoid Trabeculae and the Subarachnoid Space only about 45 to 50 g in fluid.
The arachnoid trabeculae are composed of flattened, irregu- Because the arachnoid trabeculae are not rigid, the brain may
larly shaped fibroblasts that bridge the subarachnoid space in a move within the fluid-filled subarachnoid space. In a closed head
random fashion (Fig. 7.3). Trabecular cells attach to the barrier injury, the brain may move on its trabecular tethers in response to
layer and may attach to each other, to pial cells, or to blood ves- a sudden blow and be subjected to minor damage (concussion or
sels in the subarachnoid space. Although much of the extracel- contusion). This injury may result in no or only momentary loss
lular collagen associated with trabecular cells is confined in the of consciousness. Such a minor injury may be found at the point
folded processes of these cells, some may be found free in the of the blow or at a site opposite the contact (contrecoup injury).
subarachnoid space. The attachments of the trabecular cells and
their framework of collagen fibrils give added strength to the Arachnoid Villi
arachnoid mater. The small specialized portions of the arachnoid that protrude
The subarachnoid space is located internal to the barrier cell into the superior sagittal sinus through openings in the dura form
layer and external to the pia mater (Figs. 7.2 and 7.3). This the arachnoid villi or arachnoid granulations (Figs. 7.7 and 7.8).
space, and its contiguous cisterns, contain CSF, trabecular cells If they are especially large or calcified (as in older persons), they
and collagen fibrils, arteries and veins, and the roots of cranial may be called pacchionian bodies.
nerves. Although some vessels may lie free in the subarachnoid Arachnoid villi extend into the sinus through tight cuffs in the
space, most are covered by a thin layer of the leptomeninges (Fig. meningeal dura and are found just off the midline or in cul-de-
7.3). These vessels may be damaged from trauma or may rupture sacs (the lateral or venous lacunae) of the sinus (Figs. 7.7 and
spontaneously, resulting in the spread of blood around the brain; 7.8). The vast majority of arachnoid villi are located in the lateral
this event is a subarachnoid hemorrhage. CSF is produced by lacunae of the superior sagittal sinus (see also Fig. 7.11). The
the choroid plexuses of the lateral, third, and fourth ventricles. space in the center of each villus is continuous with the subarach-
It exits the ventricular system via the foramina of Magendie and noid space around the brain. This space is enclosed in a layer
Luschka to enter the subarachnoid space (arrows in Fig. 7.2). of cells that are markedly similar to arachnoid barrier cells, and
After circulating around the brain and spinal cord, CSF reen- these arachnoid cells, in turn, are surrounded by a capsule of cells
ters the vascular system primarily through the arachnoid villi, that are essentially the same as dural border cells. These two lay-
although a small amount enters the lymphatic vessels via the ers are continuous with their respective meningeal layers through
nasal mucosa (see Chapter 6). The subarachnoid space around the stalk of the villus (Fig. 7.7). The endothelial lining of the
the spinal cord is the route used to administer spinal anesthesia. sinus is reflected onto the villus and may cover this structure
Although it is common to refer to the brain as “floating” in the entirely or may leave a few arachnoid cells exposed; the exposed
CSF of the subarachnoid space, it is actually suspended within cells are called arachnoid cap cells. The endothelium covering
this space. The structural basis for this fact is as follows. The dura the villus sits on a basement membrane, beneath which some
is adherent to the skull, the arachnoid to the dura, the arachnoid extracellular collagen may be found.
trabeculae to the pia, and the pia to the surface of the brain. Con- Arachnoid villi are structurally adapted for the transport of
sequently, the brain is suspended, through this chain, within the CSF from the subarachnoid space into the venous circulation
114 Regional Neurobiology
Lateral
lacunae Arachnoid villi in
lateral lacunae
of the SSS
B Arachnoid villus in SSS Fig. 7.9 Axial magnetic resonance (T1-weighted) image of a meningioma in the
frontal lobe of a 62-year-old woman. Note the sharp interface between the tumor
Fig. 7.8 A superior view of the superior sagittal sinus (A) and a detail (B) show-
and the brain (arrows) and the midline shift. The tumor is clearly external to the
ing the sinus and the arachnoid granulations, which are found primarily in the
brain substance.
lateral lacunae.
Meningioma
Parasagittal
Falcine
Convexity
Sellar or
suprasellar
Meningioma
A
Olfactory groove
Sphenoid wing
Sellar or
suprasellar Whorl
Of the clivus
Of the foramen
magnum
Septa
Septa
Petrosal
B Psammoma body
Fig. 7.10 Coronal view of the brain (A) and a view of the base of the skull (B)
illustrating the locations of meningiomas. In these examples, note that the name
of this tumor usually signifies its position in relation to a meningeal reflection or B
bony landmark.
C
Fig. 7.12 Histologic features of a meningotheliomatous (syncytial) meningioma
(A), a transitional meningioma (B), and a fibroblastic meningioma (C). Sheets of
elongated cells and structures suggesting whorls (arrows) are seen in the syncy-
tial tumor (A). Thin septa of elongated fibroblasts are insinuated between obvious
whorl formations in the transitional tumor (B); note the psammoma body. The
fibroblastic tumor contains many elongated cells forming sheets of various sizes (C).
Skull
Epidural hematoma
Vessel
Endothelium
Periosteal dura
Venous sinus
Meningeal dura
Dural
border cells Meningeal dura
Arachnoid
barrier cells Falx cerebri
Vein in SAS
Pia mater
Brain Subarachnoid space
(SAS)
Fig. 7.13 The relationship of extravasated blood to the meninges. The epidural hematoma is located
between the dura and the skull. Bleeding into the dura-arachnoid interface, classically called a subdural
hematoma, is actually into a structurally weak cell layer at this juncture.
Neurologic symptoms or signs in patients with meningioma are intracranial pressure. These deficits are, in order of occurrence,
generally due to compression of brain structures, involvement of headache, confusion and disorientation, lethargy, and finally a
cranial nerves, or secondary causes such as edema. In addition, state of unresponsiveness. In some cases of head trauma, the
these patients may present with seizures or with slowly devel- patient may initially be rendered unconscious, followed by a
oping personality or behavioral changes that may (or may not) lucid interval (the patient is wide awake and conversant), then
accompany specific deficits related to cranial nerve or long tract subsequently deteriorates rapidly and dies; this is called talk and
involvement. die. Keeping this in mind, it is essential to observe these patients
The treatment of choice for meningioma is surgical removal. closely.
The location of the mass may dictate the ease or difficulty of In contrast to extradural hemorrhages, bleeding into the
its removal. A convexity meningioma is rather straightforward, meninges at the junction of the arachnoid with the dura origi-
whereas a parasagittal tumor is more complex because of its nates mainly from venous structures. A common cause is the
potential involvement of the superior sagittal sinus. In like man- tearing of “bridging veins” as they pass through the subarachnoid
ner, meningiomas in the region of the cavernous sinus may involve space and enter a dural venous sinus (Fig. 7.13). Although these
branches of cranial nerves III, IV, V, and VI or the internal carotid lesions are commonly called subdural, as noted previously, there
artery; a tumor of the sella may envelop optic structures. Radia- is no naturally occurring space at the arachnoid-dura junction.
tion therapy may be used to treat specific types of meningiomas, Hematomas at this junction are usually caused by extravasated
but chemotherapy has not proven to be particularly effective. blood that splits open the dural border cell layer (Figs. 7.13 and
7.15). In contrast to epidural lesions, so-called subdural hemato-
MENINGEAL HEMORRHAGES mas appear “long and thin” because they are not constrained by
At this point, it is appropriate to consider meningeal hemorrhages any dural attachments (Fig. 7.15). This extravascular blood does
that are specifically related to the dura-skull interface and to the not collect within a preexisting space but rather creates a space
arachnoid-dura interface. These lesions share the common fea- at the dura-arachnoid junction. Because these so-called subdural
ture of being most likely caused by trauma. hematomas are usually found within a specific layer of cells, they
actually constitute “dural border” hematomas. These lesions
Extradural and “Subdural” Hemorrhages generally contain blood in their central area and myofibroblasts,
If we exclude, for the moment, subarachnoid hemorrhages, which fibroblasts, mast cells, proliferating blood vessels, and dural bor-
are considered later in this chapter, meningeal hemorrhages can der cells in the surrounding capsule.
be generally described as extravasated blood that strips the dura
from the skull or dissects open the dural border cell layer (Fig. Hygroma
7.13). The most common cause in both situations is an injury Trauma to the skull (present in 35% or more of cases) may also
to the head, with or without skull fracture. In a head injury, the result in tearing of the arachnoid membrane. In such instances,
periosteal dura may be traumatically loosened from the skull CSF, which is under pressure (100 to 180 mm H2O in a recum-
with consequent damage to a major artery; the middle and acces- bent position), also may dissect open and collect within the dural
sory meningeal arteries are common victims. Extravascular blood border cell layer. These lesions are called hygromas. These may
dissects the periosteal dura from the skull and collects to form present as a simple hygroma (CSF only) or a complex hygroma
an extradural (epidural) hematoma (Figs. 7.13 and 7.14). These (CSF plus subdural, epidural, or blood in the brain parenchyma).
lesions tend to be lenticular and appear “short and wide” owing
to the fact that they do not cross the dural attachment at suture Pia Mater
lines (Fig. 7.14). The neurologic deficits seen in patients with The pia mater consists of flattened cells with long, equally flat-
epidural hemorrhage are usually those characteristic of increased tened processes that closely follow all the surface features of the
The Meninges 117
A B
Fig. 7.14 A and B, Examples of epidural hematomas (arrows) in computed tomography scans on the
patient’s right side. The smaller lesion in A is obviously of traumatic origin; this patient has soft tissue
damage, a fractured skull, blood in the substance of the brain, and blood in the anterior horn of the lateral
ventricle and in the third ventricle. The cause of the larger lesion (B) is not obvious. Compare the shape of
these lesions with that of a “subdural” hematoma in Fig. 7.15.
Skull
Skull
Cisterns
Lamina terminalis
Superior (quadrigeminal)
Ambient Cerebellopontine
Lateral cerebellomedullary Chiasmatic
Dorsal cerebellomedullary Interpeduncular
(cisterna magna) Prepontine
Fig. 7.16 The locations of the major subarachnoid cisterns in relation to brain structures. Although the
cerebellopontine, lateral cerebellomedullary, and ambient cisterns are located on the lateral aspect of the
brainstem, their approximate positions are indicated on this midsagittal view. Compare with Table 7.1.
for evaluation of a variety of CNS disorders. A needle that is found in or next to the cistern. For example, an aneurysm pro-
introduced into the lumbar cistern (spinal tap or lumbar punc- truding into the interpeduncular cistern may affect the oculomo-
ture) between the third and fourth or the fourth and fifth lumbar tor nerve (Table 7.1) and consequently eye movements or pupil
vertebrae is the primary method used to collect a sample of CSF size. Knowledge of the nerves and vessels in the various cisterns
from this cistern (see Fig. 9.2). is a valuable diagnostic skill (Fig 7.16; Table 7.1).
Table 7.1 Some Principal Cisterns and the Main Arteries, Veins, Cranial Nerves, and Other Structures Associated with Them
CISTERN ARTERIES VEINS CRANIAL NERVES STRUCTURES
Ambient Portions of posterior cerebral, Basal vein (of Rosenthal) Trochlear Lateral aspect of crus cerebri
quadrigeminal, and supe-
rior cerebellar arteries
Cerebellopontine (infe- Vertebral artery and proximal Retroolivary and lateral Glossopharyngeal, vagus, spinal Pyramid, inferior olivary eminence,
rior; also called lateral branches of PICA medullary veins accessory, and hypoglossal and choroid plexus
cerebellomedullary)
Cerebellopontine Distal branches of anterior Pontomesencephalic and Trigeminal, facial, and
(superior) inferior cerebellar, labyrin- petrosal veins vestibulocochlear
thine, and basilar arteries
Chiasmatic Ophthalmic artery and small Optic nerve and optic chiasm
branches to chiasm and
hypophysis
Cisterna magna Distal branches of PICA, Tonsillar and dorsal Roots of C1, C2
(also called dorsal posterior spinal artery, and medullary veins
cerebellomedullary) branches to choroid plexus
of fourth ventricle
Interpeduncular Rostral end of basilar artery Portions of basal vein Oculomotor root Mammillary body, medial edge of
and portions of posterior (of Rosenthal) crus cerebri
cerebral, choroidal, and
thalamogeniculate arteries
Prepontine Basilar artery and its branches Pontine veins Abducens
Quadrigeminal Portions of posterior cerebral, Great cerebral vein (of Trochlear root Pineal, superior and inferior colliculi
quadrigeminal, and choroi- Galen)
dal arteries
Data from Yasargil MG. Microneurosurgery. Vol I: Microsurgical Anatomy of the Basal Cisterns and Vessels of the Brain, Diagnostic Studies, General Operative Techniques and Pathological
Considerations of the Intracranial Aneurysms. Stuttgart: Georg Thieme; 1984.
PICA, posterior inferior cerebellar artery.
5 1
2
1
4 2
A B
Fig. 7.17 Magnetic resonance images in sagittal (A) and axial (horizontal, B) planes with some of the
major cisterns indicated: 1, interpeduncular; 2, superior (quadrigeminal); 3, cisterna magna (dorsal cer-
ebellomedullary); 4, prepontine; 5, of the lamina terminalis; 6, ambient.
time of the hemorrhage may describe the headache as “explosive subarachnoid hemorrhage (leaking aneurysm). These include
and awful,” or “the absolutely worst headache I have ever had.” intermittent headache, nausea or vomiting, and fainting spells
This is commonly called a “thunderclap headache.” A sudden (syncope). In persons with neurologic signs that can be traced to
headache that clears (a warning or sentinel headache) may sig- an aneurysm, the treatment of choice is to clip the aneurysm or its
nal an impending aneurysmal repture or intracranial bleed. Bloody stalk, thereby separating it from the cerebral circulation.
CSF obtained by lumbar or cisternal puncture is diagnostic of sub-
arachnoid hemorrhage, and blood can be clearly identified in the Meningitis
subarachnoid space on CT examination (Fig. 7.19). In some cases, Meningeal infection may be of either bacterial or viral ori-
a patient may have warning signs and symptoms of an impending gin or occur as a sequel to some other disease process, such as
120 Regional Neurobiology
Dural border
cells
Arachnoid
barrier cells
SAS Arachnoid
trabeculae
Subarachnoid
space (SAS)
Artery in SAS
Pia mater
Blood
between
frontal
lobes
Sylvian
cistern
Midbrain Interpeduncular
cistern
Superior
cistern Ambient cistern
rather than days), and the onset is slow and characterized by altered level of consciousness. In a minority of cases, more serious
headache, fever, irritability, and wakefulness at night. In acute, signs and symptoms may be seen, such as seizures, rigidity, or cra-
subacute, and chronic meningitis, the prognosis is excellent nial nerve palsies. Treatment in mild cases is supportive and gener-
(with about a 90% cure rate) with early diagnosis and proper ally focuses on medications for fever, pain, and general discomfort.
treatment. After an acute period of 1 to 2 weeks, the signs and symptoms
Viral meningitis is caused by a range of viral agents, is most moderate, and the patient generally recovers without permanent
commonly seen in younger patients (younger than 25 years), and deficits.
is a disease for which no antiviral medications are available. The
patient becomes ill during a period of days and experiences fever, Sources and Additional Reading
headaches of increasing intensity, and confusion and possibly an The complete list is available online at www.studentconsult.com.
Sources and Additional Reading Peters A, Palay SL, Webster HD. The Fine Structure of the Nervous System:
Alcolado R, Weller RO, Parrish EP, Garrod D. The cranial arachnoid and pia Neurons and Supporting Cells. 3rd ed. Philadelphia: WB Saunders; 1991.
mater in man: Anatomical and ultrastructural observations. Neuropathol Appl Ropper AH, Samules MA, Klein JP. Adams and Victor’s Principles of Neurology.
Neurobiol. 1988;14:1–17. 10th ed. New York: McGraw-Hill Education; 2014.
Al-Mefty O. Meningiomas. New York: Raven Press; 1991. Rowland LP, Pedley TA, eds. Merritt’s Neurology. 12th ed. Baltimore: Lippin-
Frederickson RG. The subdural space interpreted as a cellular layer of meninges. cott Williams & Wilkins; 2010.
Anat Rec. 1991;230:38–51. Schachenmayr W, Friede RL. The origin of subdural neomembranes: I. Fine
Greenberg MS. Handbook of Neurosurgery. New York: Thieme; 2010. structure of the dura-arachnoid interface in man. Am J Pathol. 1978;92:
Haines DE. On the question of a subdural space. Anat Rec. 1991;230:3–21. 53–68.
Haines DE, Harkey LH, Al-Mefty O. The “subdural space”: a new look at an Van Denabeele F, Creemans J, Lambrichts I. Ultrastructure of the human spinal
outdated concept. Neurosurgery. 1993;32:111–120. arachnoid mater and dura mater. J Anat. 1996;189:417–430.
Nabeshima S, Reese TS, Landis DMD, Brightman MW. Junctions in the menin- Williams PL, ed. Gray’s Anatomy. 38th ed. New York: Churchill Livingstone;
ges and marginal glia. J Comp Neurol. 1975;164:127–170. 1995.
Nicholas DS, Weller RO. The fine anatomy of the human spinal meninges. J Yasargil MG. Microneurosurgery. Vol. I: Microsurgical Anatomy of the Basal
Neurosurg. 1988;69:276–282. Cisterns and Vessels of the Brain, Diagnostic Studies, General Operative
Orlin JR, Osen K, Hovig T. Subdural compartment in pig: a morphologic Techniques and Pathological Considerations of the Intracranial Aneurysms.
study with blood and horseradish peroxidase infused subdurally. Anat Rec. Stuttgart, Germany: Georg Thieme; 1984.
1991;230:22–37.
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