Introduction To Brain Anatomy: Wieslaw L. Nowinski
Introduction To Brain Anatomy: Wieslaw L. Nowinski
2.1Introduction
The human central nervous system (CNS), having been evolved over the last 600
million years, is the most complex living organ in the known universe. It has been
extensively investigated over centuries, and a vast body of materials has been
gathered in the print form and more recently also in electronic format. Neuroanatomy
is presented in numerous textbooks [122], print brain atlases [2351], and electronic
brain atlases [5274]. Several textbooks combine text with atlases [14, 15, 43, 44],
and some provide neuroanatomy for various specialties including neurosurgery
[1,19, 22], neuroradiology [8, 17, 20], neurology [2], and neuroscience [18].
The comprehension of neuroanatomy is crucial in any neurosurgical, neuroradiological, neuro-oncological, or neurological procedure. Therefore, CNS anatomy
has been intensively studied by generations of neuroanatomists, neurosurgeons,
neurologists, neuroradiologists, neurobiologists, and psychologists, among others,
including Renaissance artists. This resulted, however, in neuroanatomy discrepancies, inconsistencies, and even controversies among various communities in terms
of parcellation, demarcation, grouping, terminology, and presentation.
The present work differs from existing neuroanatomy primers. Our overall objective
is to make the presentation of brain anatomy easy. To achieve this objective:
The presentation of neuroanatomy is in three dimensions (3D) with additional
supportive planar images in the orthogonal (axial, coronal, and sagittal) planes.
The brain is subdivided into structure, vasculature, and connections (white matter
tracts); consequently, we consider structural, vascular, and connectional neuro
anatomies.
W.L. Nowinski
2.2.1Brain Parcellation
The CNS consists of the brain and the spinal cord. The brain encases the fluid-filled
ventricular system and is parcellated into three main components (Fig.2.1a):
Cerebrum
Cerebellum (the little brain)
Brainstem
The cerebrum comprises:
Left and right cerebral hemispheres
Interbrain between the cerebrum and the brainstem termed the diencephalon
Deep gray nuclei
The cerebral hemispheres are the largest compartment of the brain and are interconnected by white matter fibers (see Sect.2.4.2). The hemispheres are composed of:
Outer gray matter termed the cerebral cortex
Inner white matter encompassing the deep gray nuclei
Fig.2.1 Gross anatomy of the left cerebral hemisphere: (a) brain parcellation; (b) lobes: lateral
view; (c) lobes: medial view
W.L. Nowinski
Fig.2.1 (continued)
The gray matter contains mainly nerve cell bodies, while the white matter is made
up predominantly of nerve fibers (axons). The cerebral cortex is highly convoluted.
The folds form gyri that are separated by grooves called sulci or fissures (deep
sulci). The cerebral hemispheres are parcellated into five lobes (Fig.2.1b, c):
Frontal lobe
Temporal lobe
Parietal lobe
Occipital lobe
Limbic lobe
The insula is sometimes classified as the central or insular lobe. The lobes are
partly demarcated by the sulci/fissures, Fig.2.1. The central sulcus separates the
frontal lobe anterior from the parietal lobe posterior, Fig.2.1b. The Sylvian (lateral)
fissure demarcates the temporal lobe below from the frontal and parietal lobes
above, Fig.2.1b. The parieto-occipital fissure separates the parietal lobe anterior
from the occipital lobe posterior, Fig. 2.1c. The cingulate sulcus separates the
frontal lobe above from the limbic lobe below, Fig.2.1c.
The diencephalon contains (Fig.2.1c):
Thalamus (see also Fig.2.6)
Subthalamus including the subthalamic nucleus (see Sect.2.2.6)
Hypothalamus (see also Fig.2.10a)
Fig.2.2 Cerebellum and brainstem: (a) cerebellum (medial view); (b) midbrain, pons, and medulla
of the brainstem (infero-anterior view)
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W.L. Nowinski
Fig.2.3 Cortical areas of the left (L) hemisphere: lateral view. The orientation cube in the top-left
corner indicates the viewing direction (L left; R right; S superior (dorsal); I inferior (ventral);
A anterior; P posterior). Each gyrus is assigned a unique color
2.2.2Cortical Areas
The cortex has three surfaces: lateral, medial, and inferior (also called basal or
ventral). Moreover, the transitional areas form the frontal, temporal, and occipital
poles (see, e.g., Figs.2.5 and 2.27).
2.2.2.1Lateral Surface
Four lobes are present on the lateral surface: frontal, temporal, parietal, and occipital,
Fig.2.1b. The lateral surface of the frontal lobe is subdivided by three sulci (superior
frontal sulcus, inferior frontal sulcus, and precentral sulcus) into four gyri (Fig.2.3):
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The lateral surface of the temporal lobe is subdivided by two sulci (superior temporal
sulcus and inferior temporal sulcus) into three gyri (Fig.2.3):
Superior temporal gyrus
Middle temporal gyrus
Inferior temporal gyrus
The lateral surface of the parietal lobe is subdivided by the intraparietal sulcus
into three gyri (Fig.2.3):
Postcentral gyrus
Superior parietal gyrus (lobule)
Inferior parietal gyrus (lobule)
Supramarginal gyrus
Angular gyrus
The lateral surface of the occipital lobe is subdivided by two sulci (superior
occipitalsulcus and inferior occipital sulcus) into three gyri (Fig.2.3):
Superior occipital gyrus
Middle occipital gyrus
Inferior occipital gyrus
2.2.2.2Medial Surface
The frontal, parietal, occipital, and limbic lobes are present on the medial surface,
Fig.2.1c. The limbic lobe contains the gyri located at the inner edge (or limbus) of
the hemisphere including (Fig.2.4):
The superior frontal gyrus (separated from the limbic lobe by the cingulate sulcus, Fig.2.1c) occupies most of the medial surface of the frontal lobe, Fig.2.4. The
parietal lobe includes the precuneus, Fig.2.4 (separated from the occipital lobe by
the parieto-occipital fissure, Fig.2.1c). The occipital lobe comprises the cuneus and
the lingual gyrus, Fig.2.4.
2.2.2.3Inferior Surface
The inferior surface includes the frontal, temporal, and occipital lobes. The frontal
lobe comprises (Fig.2.5):
Straight gyrus
Orbital gyri parcellated by the approximately H-shape sulcus into the anterior,
medial, lateral, and posterior orbital gyri
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The temporal and occipital lobes are subdivided by two sulci (lateral occipitotemporal
sulcus and medial occipitotemporal (collateral) sulcus) into three gyri, Fig.2.5:
Medial occipitotemporal gyrus whose temporal part constitutes the parahippocampal gyrus and the occipital part the lingual gyrus
Lateral occipitotemporal gyrus (called also the fusiform gyrus)
Inferior temporal gyrus
The lingual gyrus is separated from the cuneus by the calcarine sulcus (fissure).
2.2.4Ventricular System
The ventricular system contains four interconnected cerebral ventricles (cavities)
filled with cerebrospinal fluid (CSF) (Fig.2.7a):
Left and right lateral ventricles
Third ventricle
Fourth ventricle
CSF is secreted mainly in the choroid plexus (a network of vessels) and circulates
from the lateral ventricles through the paired interventricular foramina (of Monro)
to the third ventricle, and then via the aqueduct to the fourth ventricle, Fig.2.7a.
Thelateral ventricles are the largest and each contains (Fig.2.7b):
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Fig.2.6 Deep gray nuclei: (a) embedded into the brain; (b) shown in isolation
W.L. Nowinski
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Fig.2.7 Ventricular system: (a) interconnected ventricles; (b) components of the lateral ventricle
2.2.5Sectional Neuroanatomy
Sectional (planar) neuroanatomy is typically presented on orthogonal (axial, coronal,
and sagittal) images. To spatially locate the orthogonal images, we place them in the
Talairach coordinate system [48], which is a stereotactic reference system based on
the anterior and posterior commissures (see also Fig.2.28a) with the origin at the
center of the anterior commissure (see also Figs.2.82.10).
Four axial images located at 12, +1, +12, and +24mm (where denotes the
level below and + above the anterior commissure) with the cortical areas and deep
gray nuclei segmented and labeled are shown in Fig.2.8.
Two coronal images passing through the anterior and posterior commissures are
presented in Fig.2.9.
Two sagittal images located at 3 and 21 mm from the midline are shown in
Fig.2.10.
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W.L. Nowinski
Anterior
32mm
Superior frontal gyrus
Middle frontal gyrus
TT88a /12mm
Amygdaloid body
Ventricle(s)
Left
Right
Hippocampus
Lingual gyrus
Fusiform gyrus
Hippocampal gyrus
Posterior
Anterior
32mm
Cingulate gyrus
Superior frontal gyrus
Middle frontal gyrus
Corpus callosum
TT88a/+1mm
Caudate nucleus
Insula
Superior temporal gyrus
Hippocampus
Left
Right
Putamen
Cuneus
Lingual gyrus
Posterior
Fig. 2.8 Planar neuroanatomy in axial orientation at: (a) 12 mm; (b) +1 mm (along with
theTalairach grid); (c) +12mm; (d) +24mm ( denotes the level below and + the level above the
anterior commissure)
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Anterior
Superior frontal gyrus
TT88a/12mm
Cingulate gyrus
32mm
Corpus callosum
Inferior frontal gyrus
Caudate nucleus
Putamen
Left
Right
Precentral gyrus
Hippocampus
Middle temporal gyrus
Thalamus: Pulvinar nucleus
Middle occipital gyrus
Caudate nucleus
Cuneus
Corticospinal tract: inf. limb
Posterior
Anterior
32mm
Superior frontal gyrus
Middle
frontal
gyrus
Cingulate gyrus
TT88a/+24mm
Ventricle(s)
Precentral gyrus
Postcentral gyrus
Left
Right
Caudate nucleus
Corpus Callesum
Inferior parietal lobule
Middle temporal gyrus
Cingulate gyrus
Precuneus
Cuneus
Posterior
Fig.2.8 (continued)
Occipital gyri
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W.L. Nowinski
Dorsal
TT88c / 0mm
32mm
Corpus callosum
Cortical areas
Ventricle(s)
Precentral gyrus
Putamen
Left
Right
Caudate nucleus
Amygdaloid body
Globus pallidus medial segment
Hypothalamus: Lateral preoptic
nucleus
TT88c / -24mm
Ventral
Dorsal
Precentral gyrus
16mm
Left
Right
Cortical areas
Caudate nucleus
Ventricle(s)
Corpus callosum
Thalamus: Pulvinar nucleus
Hippocampus
Caudate nucleus
Ventricle(s)
Ventral
Fig.2.9 Planar neuroanatomy in coronal orientation at: (a) 0mm passing through the anterior
commissure (point), i.e., the location on the coronal plane where the horizontal and vertical planes
of the Talairach system intersect; (b) 24mm passing through the posterior commissure (point)
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Dorsal
TT88s/L+3mm
8mm
Anterior commissure
Hypothalamus: Dorsal nucleus
Anterior
Posterior
Hypothalamus: Ventromedial
nucleus
Hypothalamus: Medial preoptic
nucleus
Hypothalamus: Supra-optic nucleus
Ventral
Dorsal
TT88s/L+21mm
16mm
Anterior
Putamen
Anterior commissure
Hippocampus
Amygdaloid body
Cortical areas
Caudate nucleus
Ventral
Fig.2.10 Planar neuroanatomy in sagittal orientation at: (a) 3mm (along with the Talairach grid);
(b) 21mm from the midline
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W.L. Nowinski
TT88s/L+9mm
Dorsal
8mm
TT88a/4mm
SW
Anterior
SW
t8
t8
Anterior
Posterior
TT88c/12mm
Left
Right
t9
Posterior
Dorsal
SW
t8
Left
Right
t9
Subthalamic nucleus
Ventral
Ventral
Fig.2.11 Subthalamic nucleus on sagittal, axial, and coronal planes (the location of the triplanar
is marked by the green dashed lines)
Fig.2.12 Ventrointermediate nucleus of the thalamus: sagittal, coronal, and axial planes
Anterior
21
8mm
SW
TT88c /4mm
Dorsal
t8
SW
t8
Left
Right
t9
Right
Ventral
TT88s/ L+13mm Dorsal
SW
t8
t9
Anterior
Posterior
Posterior
Ventral
Fig.2.13 Globus pallidus interna (medial segment): axial, coronal, and sagittal planes
Fig.2.14 Stereotactic target structures in 3D. The marks on the axes are placed at 10-mm intervals
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W.L. Nowinski
2.2.7Functional Areas
Several parcellations are introduced to subdivide the cortical regions into functional
areas [16]. Brodmanns parcellation based on histology is the most widely used and
it is illustrated in axial orientation in Fig. 2.15. Brodmanns areas are useful in
neuroscience and functional studies.
2.3Vascular Neuroanatomy
The knowledge of cerebrovasculature is crucial in stroke, vascular and tumor surgery
as well as interventional neuroradiology. The complete cerebrovasculature is highly
complex and variable, Fig.2.16. It is subdivided into:
Arterial system
Venous system with the cerebral veins and dural sinuses
a
TT88a / +8mm
Brodmanns area 10
Areas 10 and 19 belong to the prefrontal
cortex. Principal connections are with the
thalamus (dorsomedian nucleas) and
also the three other cerebral lobes, and
the hypothalamus. Efferent fibers,
associated with others from areas 8 and
45, accompany the tract of Arnold to the
brainstem.
Anterior
Brodmanns area 10
Brodmanns area 45
Areas 45 and 44 cover approximately the
cortical area of Broca (motor speech) in
the lower frontal convolution. They are
directly connected by long tract with area Brodmanns area 45
10 and undoubtedly with the
supplementary motor area.
Brodmanns area 37
Area 37 is an auditory visual association
area.
Brodmanns area 37
Brodmanns area 17
Area 19 is largely interconnected with the
adjacent areas and contralateral area 19
via callosal radiations. The occipital
Brodmanns area 17
oculomotor area on the external surface of
Area 17 is the primary visual sensory area
the lobe spreads over areas 18 and 19. It Brodmanns area 19
Brodmanns area 17 macroscopically identified by the striae of
is the seat of vertical and oblique
Gennari. It is directly connected with area
conjugate movements of automatic type.
18 and through it with area 19.
frontal oculomotor center, to the
Brodmann s area 18
sensorimotor cortex, and to the auditory
Brodmanns area 10
cortex by long association bundles.
Area 18 is the area of visual integration
possessing reciprocal connection with
area 19. Efferent fibers travel subcortically
toward the brainstem of the superior
quadrigeminal colliculus. The occipital
oculomotor area on the external surface of
the lobe spreads over areas 18 and 19. It
is the seat of vertical and oblique
conjugate movements of automatic type.
Areas 18 and 19 are connected to the
frontal oculomotor center, to the
sensorimotor cortex, and to the auditory
cortex by long association bundles
Fig.2.15 Brodmanns areas in axial orientation: (a) vision and speech areas (+8mm); (b) motor
and sensory areas (+40mm). The areas are uniquely color-coded
Fig.2.15 (continued)
Fig.2.16 The cerebral vasculature with arteries, veins, and dural sinuses. The vessels are uniquely
color-coded such that all vessels with the same name have the same color
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W.L. Nowinski
2.3.1Arterial System
2.3.1.1Parcellation of Arterial System
The brain is supplied by two pairs of arteries:
Left and right internal carotid arteries anteriorly
Left and right vertebral arteries posteriorly forming the basilar artery (Fig.2.17a)
interconnected by the circle of Willis (Fig.2.21).
The internal carotid artery (ICA) branches into the anterior cerebral artery
(Fig.2.17c) and the middle cerebral artery (Fig.2.17d). The left and right posterior
cerebral arteries originate from the basilar artery (Fig.2.17e).
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Fig.2.17 The cerebral arteries: (a) blood supply to the brain by the internal carotid artery (ICA)
anteriorly, and the vertebral artery (VA) and the basilar artery (BA) posteriorly; (b) ICA and VA
connected by the circle of Willis; (c) anterior cerebral artery along with the ICA, VA, and BA;
(d)middle cerebral artery along with the ICA, VA, and BA; (e) posterior cerebral artery along with
the ICA, VA, and BA; (f) complete arterial system
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W.L. Nowinski
2.3.1.5Circle of Willis
The circle of Willis connects the anterior and posterior circulations. It includes the
following vessels (Fig.2.21):
2.3.2Venous System
2.3.2.1Parcellation of Venous System
The main components of the venous system are, Fig.2.22:
Dural sinuses
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Fig.2.19 Middle cerebral artery: (a) M1, M2, M3, and M4 segments; (b) main branches of the
left hemisphere
Cerebral veins
Superficial veins
Deep veins
The cerebral veins empty into the dural sinuses.
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W.L. Nowinski
2.3.2.2Dural sinuses
The main dural sinuses are (Fig.2.23):
2.3.2.3Cerebral Veins
The main superficial cerebral veins are (Fig.2.24):
Frontopolar veins
Prefrontal veins
Frontal veins
Parietal veins
Occipital veins
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2.3.3Vascular Variants
The human cerebrovasculature is highly variable and vascular variants have been
extensively studied, see e.g., [6, 10, 13, 22]. Variations exist in terms of origin, location, shape, size, course, branching patterns as well as surrounding vessels and
structures. The knowledge of cerebrovascular variants is central in diagnosis,
treatment, and medical education.
Main variants in 3D in the circle of Willis are show in Fig.2.26 (more 3D variants
are presented in [70]).
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W.L. Nowinski
Fig.2.22 Parcellation of the venous system: (a) dural sinuses (DS); (b) superficial veins with the
DS; (c) deep veins with the DS; (d) complete venous system
2.4Connectional Neuroanatomy
Three types of white matter connections (or tracts, fibers, bundles, fiber pathways,
fascicles) are distinguished in the cerebral hemispheres (Fig.2.27):
Commissural tracts
Association tracts
Projection tracts
In addition, three cerebellar paired peduncles:
Superior peduncle
Middle peduncle
Inferior peduncle
connect the cerebellum to the midbrain, pons and medulla of the brainstem,
respectively.
31
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W.L. Nowinski
Fig. 2.26 Vascular variants of the circle of Willis: (a) double anterior communicating artery;
(b) absent left posterior communicating artery; (c) absent left P1 segment (the variants are in white)
2.4.1Commissural Tracts
The commissural tracts interconnect both hemispheres across the median plane.
The main commissural tracts are, Fig.2.28:
Corpus callosum
Anterior commissure
Posterior commissure
The corpus callosum (the great commissure) is the largest commissure. Its three
main parts, genu (knee), body, and splenium, connect the frontal lobes, wide areas
of hemispheres, and the occipital lobes, respectively.
The anterior commissure connects the temporal lobes, while the posterior
commissure the midbrain, thalamus, and hypothalamus on both sides.
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Fig.2.27 White matter tracts on the left and for comparison the brain on the right
2.4.2Association Tracts
The association tracts interconnect different cortical regions of the same hemisphere. There are two types of the association tracts:
Short arcuate fibers that connect adjacent gyri (U fibers)
Long arcuate fibers interconnecting widely separated gyri
The main association tracts are (Fig.2.29):
The superior longitudinal fasciculus connects the frontal lobe with the temporal,
parietal, and occipital lobes. The inferior longitudinal fasciculus links the temporal
lobe with the occipital lobe. The cingulum deep to the cingulated gyrus interconnects
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W.L. Nowinski
Fig. 2.28 Commissural tracts with the corpus callosum, anterior commissure, and posterior
commissure: (a) on the midsagittal plane; (b) in 3D
parts of the temporal, parietal, and occipital lobes. The uncinate fasciculus connects the
frontal lobe (orbital gyri and motor speech area) with the temporal lobe.
2.4.3Projection Tracts
The projection tracts connect the cortex with the subcortical structures in the diencephalon, brainstem, and spinal cord. The main projection tracts are (Fig.2.30):
Cortico-spinal (pyramidal) tract
Cortico-thalamic tract including the anterior, posterior (optic), and superior
thalamic radiations
Cortico-bulbar tract (connecting to the brainstem)
Cortico-pontine tract (projecting to the cerebellum)
Auditory radiations
The projection fibers between the striatum and thalamus form the internal
c apsule consisting of the anterior limb (containing the cortico-thalamic tract), genu
(comprising the cortico-bulbar tract), and posterior limb (containing the corticospinal tract). The fibers radiating from the internal capsule to various parts of the
cerebral cortex form the corona radiata.
2.5Summary
The brain contains the cerebrum, cerebellum, and brainstem, and it encases the
ventricular system. The cerebrum comprises the paired cerebral hemispheres and deep
gray matter nuclei including the caudate nucleus, putamen, lateral and medial globus
35
36
W.L. Nowinski
Fig.2.30 Projection tracts of the right hemisphere along with the thalamus
This introduction covers basic neuroanatomy. For further study, the reader is
referred to the existing literature and electronic atlases.
Acknowledgments I am deeply grateful to Drs. J Talairach and P Tournoux for the insightful
discussions about their atlases.
Numerous persons from our Biomedical Imaging Lab, A*STAR, Singapore, have contributed
to the development of tools for atlas construction and atlas-assisted applications. The key
contributorsare BC Chua, A Thirunavuukarasuu, Y Marchenko, GY Qian, and I Volkau (the references
[6470, 7680, 8392] provide a more complete list of contributors). I thank Aminah Bivi for her
editorial assistance.
I am also grateful to the reviewers: an anonymous reviewer and Dr. Joseph M. Corless, MD,
PhD, Duke University Medical Center, for their valuable comments.
This work has been funded by A*STAR, Singapore.
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