Handbook of Spinal Cord Injuries and Related Disorders A Guide To Evaluation and Management 1st Edition Hyun Yoon Ko Sungchul Huh
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Hyun-Yoon Ko and Sungchul Huh
Handbook of Spinal Cord Injuries and
Related Disorders
A Guide to Evaluation and Management
1st ed. 2021
Hyun-Yoon Ko
Department of Rehabilitation Medicine, Rehabilitation Hospital, Pusan
National University Yangsan Hospital, Pusan National University
College of Medicine, Yangsan, Korea (Republic of)
Sungchul Huh
Department of Rehabilitation Medicine, Rehabilitation Hospital, Pusan
National University Yangsan Hospital, Yangsan, Korea (Republic of)
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The spinal cord controls the voluntary muscles of the trunk as well as the
upper and lower extremities and receives sensory information from the areas
of the body. It is anchored to the dura mater by denticulate ligaments and
extends from the cervicomedullary junction to the tip of the conus medullaris
at the lower border of the first lumbar vertebra, which is individually variable
(Bican et al. 2013). There are 20 or 21 pairs of denticulate ligament attached to
the anterolateral segment of the spinal cord. The spinal cord is anchored
caudally by filum terminale: filum terminale internum in the dural sac and
filum terminale externum outside the dural sac up to the coccyx. Basic
knowledge of anatomy and embryologic development, including metamerism
of the myotomes and dermatomes is very important for the interpretation and
understanding of the pathological findings of the spinal cord, as well as for the
diagnosis and lesion localization of the lesions.
Table 1.1 Vertebral bodies in their relations to corresponding spinal cord segments
1.2 Metamerism
The spinal cord is a segmental organ. Each of the 31 pairs of spinal nerves
supplies a metamere or body segment derived from an embryonic somite.
Metamerism is more evident in the thoracic than in other regions of the adult
body, and the fields of sensory innervation are easier to identify than those of
motor innervation. The outgrowth of limb buds in the embryo causes
complicated metameric patterns.
The body surface areas supplied by the nerve fibers from a single dorsal
root ganglion are defined as a dermatome. The dermatomes are orderly in the
embryo, but they are distorted by outgrowth of the limbs so that the C4
dermatome is above T2 at the level of the sternal angle. Finally, the C5
dermatome is located next to the T1 dermatome (Biller et al. 2017; Vanderah
and Gould 2016) (Fig. 1.4). The junctions are marked by “axial lines” in the
diagram. A similar relationship exists in the lower extremities. At the 8th week,
medial rotation of the lower limb reverses the preaxial and postaxial borders,
creating a spiral arrangement of dermatomes (Fig. 1.5). Spinal nerve segments
on the anterior surface of the lower extremity extend medially and inferiorly.
The great toe is supplied by nerves from a more rostral dermatome (L4) rather
than the little toe (S1). The lower extremity is an extension of the trunk, and
most caudal dermatomes supply the perineum, not the foot (Felten et al.
2016). Cervical dermatomes maintain a relatively orderly distribution in the
upper extremity with minimal rotation. Within the same spinal cord segment,
the region of the sensation is also determined by the typical topographic
organization (Altman and Bayer 2001) (Fig. 1.6). Most dermatomes overlap
one another to a varying extent, but there is less overlap with pain and
temperature than with touch. An overlap of sensory fibers, which can reach
25–40 mm, occurs along the midline (Kellgren 1939).
Fig. 1.4 Development of dermatomes of the upper extremity of human embryos. Outgrowth
of limb buds in the embryo results in complications of the metameric patterns. Finally, the C5
dermatome lies next to the T1 dermatome due to outgrowth of the upper extremities carrying
the intervening dermatomes. From Biller et al. (2017)
Fig. 1.5 Changes in ventral dermatome pattern during limb development with limb rotation.
Rotation of the lower limb results in a reversal of the preaxial and postaxial borders,
producing a spiral arrangement of dermatomes. Spinal nerve segments on the anterior surface
of the lower extremity extend medially and inferiorly; the great toe (hallux) is supplied by
nerves from a more rostral dermatome (L4) than the little toe (S1). The lower extremity is an
extension of the trunk, and the most caudal dermatomes (sacral and coccygeal) supply the
perineum, not the foot. Cervical dermatomes maintain a relatively orderly distribution to the
upper extremity with minimal rotation. From Felten et al. (2016)
Fig. 1.6 Somatotopic organization of cutaneous afferents in laminae II-III of the cervical and
upper thoracic spinal cord of the cat. Sensory fibers from the dorsal skin, arm, forearm, and
hand are arranged in a lateral to medial order. Digit II, III, and IV are represented in a rostral-
to-caudal order. From Altman and Bayer (2001)
Metamerism also occurs in the innervation of skeletal muscles. Few
muscles have been derived from a single somite. The adductor pollicis and
some of the small deep muscles of the back may have a monosegmental
innervation. Other muscles receive nerve fibers from two to five ventral roots,
especially in the upper and lower extremities (Keegan and Garrett 1948).
1.3 Myelination
Myelin formation on nerve fibers of the spinal cord occurs only in the middle of
fetal life. It is then thought to be associated with differentiation of glioblasts
into oligodendrocytes. The first myelination of axons in the human is observed
in the early fetal spinal cord at less than 16 weeks of gestation. Although not
many mammals, myelination in the human is part of the postnatal
developmental period. The earliest structure to myelinate is the medial
longitudinal fascicles in the upper cervical spinal cord at 20 weeks, with the
corticospinal tract being the last, and myelination during the first year after
birth (Armand 1982; Weidenheim et al. 1996). The process of myelin
formation continues for several years, but the exact time of its completion is
unknown (Fig. 1.7).
Fig. 1.7 Schematic summary of the myelination of the corticofugal tract. A corticospinal
tract that descends through the internal capsule, the cerebral peduncle, the pontine gray, and
crosses in the pyramid is the absence of myelin at birth. At 1 month of age, a small
complement of myelinating corticofugal fibers reaches the pontine gray. But the bulk of the
corticofugal tract remains unmyelinated. There is an increase in the proportion of myelinated
fibers in the upper corticofugal tract between 2 and 3 months. The myelination of the bulk of
the lower corticospinal tract occurs between 4 and 8 months of age. From Altman and Bayer
(2001)
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