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Chapter 17 Discography 313
psychological factors, chronic pain behavior, regional or central pain syndromes, and compensation issues.
3.
Provocative discography has not been proven to improve
outcomes of treatment for low back pain syndromes. In patients with emotional distress issues or compensation issues, there is some evidence that using discography may result in poorer outcomes and inappropriate invasive procedures.
4.
Risks of provocative discography include false and misleading
diagnoses in patients with high pain-sensitive risk factors, increased axial pain for weeks or months after injection, pyogenic discitis, and accelerated disc degeneration after long-term follow-up.

KEY REFERENCES

1. Sackett D, Haynes R. Evidence base of clinical diagnosis: the architecture of diagnostic research. BMJ. 2002;324:539-541.
This article denes the necessary conditions to establish validity and clinical usefulness of a diagnostic test. The gold standard necessary to compare diagnostic test results is of prime importance, as is a careful assessment of the study population. These conditions are problematic in the evaluation of provocative discography.
2.
Carragee EJ, Tanner CM, Yang B, et al. False-positive ndings on
lumbar discography: reliability of subjective concordance assessment during provocative disc injection. Spine. 1999;24:2542-2547.
This study looks at the reliability of the concordance response during discography. The authors found that volunteer subjects with known pelvic area pain cannot reliably distinguish the sensation coming from a pelvic pain generator from the sensation caused by the injection of an asymptomatic disc. The implications for validity of provocative injections are discussed.
3.
Ohtori S, Kinoshita T, Yamashita M, et al. Results of surgery for
discogenic low back pain: a randomized study using discography versus discoblock for diagnosis. Spine. 2009;34:1345-1348.
The authors performed a randomized clinical trial comparing outcomes of subjects having single-level fusion based on an evaluation using provocative discography with subjects having an anesthetic disc injection. These were in some respects best-case scenario subjects (no psychological distress, no depression, no worker’s compensation cases, and no trac accident litigants).
The discography was performed using low-pressure injections. The outcomes in the discography group (reported pain, function, pain medications) were uniformly worse than the group using an anesthetic block to determine fusion.
4.
Carragee EJ, Don AS, Hurwitz EJ, et al. Does discography cause
accelerated progression of degeneration changes in the lumbar disc: a ten-year matched cohort study. Spine. 2009;34:2338-2345.
Matched asymptomatic cohorts with and without baseline pressure-limited provocative discography were followed with a detailed MRI protocol compared against baseline MRI ndings. The discography group had greater progression of disc degeneration scores, more new disc herniations, greater loss of disc height, and greater loss of disc signal compared with the control group. In the discography cohort, new disc herniations were disproportionately found near the puncture site.
5.
Chou R, Loesser JD, Owens DK. Interventional therapies, surgery,
and interdisciplinary rehabilitation for low back pain: an evidence-based clinical practice guideline from the American Pain Society. Spine. 2009;34:1066-1077.
In a comprehensive multidisciplinary review, the authors concluded: “In patients with chronic nonradicular low back pain, provocative discography is not recommended as a procedure for diagnosing discogenic low back pain (strong recommendation, moderate-quality evidence).”

REFERENCES

1. Lindblom L. Diagnostic puncture of intervertebral disks in sciatica. Acta Orthop Scand. 1948;17:231-239.
2. Derby R, Guyer R, Lee S-H, et al. e rational use and limitations of provocative discography. International Spine Intervention Society 13th annual meeting, New York. ISIS Newsletter. 2004;5:6-20.
3. Walsh T, Weinstein J, Spratt K, et al. Lumbar discography in normal subjects: a controlled prospective study. J Bone Joint Surg Am. 1990;72:1081-1088.
4. Allan DB, Waddell G. An historical perspective on low back pain and disability. Acta Orthop Scand Suppl. 1989;234:1-23.
5. Burton A. Spine update: back injury and work loss: biomechanical and psychosocial inuences. Spine. 1997;22:2575-2580.
6. Burton A, Tillotson K, Main C, et al. Psychosocial predictors of outcome in acute and subacute low back trouble. Spine. 1995;20:722-728.
7. Aprill C, Bogduk N. High-intensity zone: a diagnostic sign of painful lumbar disc on magnetic resonance imaging. Br J Radiol. 1992;65:361-369.
8. Crock H. Internal disc disruption. Med J Aust. 1970;1:983-990.
9. Derby R, Howard MW, Grant JM, et al. e ability of pressure-controlled discography to predict surgical and nonsurgical outcomes. Spine. 1999;24:364-371.
10. O’Neill C, Derby R, Kanderes L. Precision injection techniques for diagnosis and treatment of lumbar disc disease. Semin Spine Surg. 1999;11:104-118.
11. Schwarzer A, Aprill C, Derby R, et al. e prevalence and clinical features of internal disc disruption in patients with chronic LBP. Spine. 1995;20:1878-1883.
12. Schwarzer A, Aprill C, Fortin J, et al. e relative contribution of the zygapophyseal joint in chronic low back pain. Spine. 1994;19:801-806.
13. Schwarzer A, Bogduk N. e prevalence and clinical features of internal disk disruption in patients with low back pain [letter]. Spine. 1996;21:776.
14. Siddle P, Cousins M. Spinal pain mechanisms. Spine. 1997;22: 98-104.
15. Carragee EJ, Tanner CM, Yang B, et al. False-positive ndings
on lumbar discography: reliability of subjective concordance assessment during provocative disc injection. Spine. 1999;24:2542-2547.
16. Carragee EJ, Tanner CM, Khurana S, et al. e rates of false-positive lumbar discography in select patients without low back symptoms. Spine. 2000;25:1373-1380.
17. Gracely R, Dubner R, McGrath P. Narcotic analgesia: fentanyl reduces the intensity but not the unpleasantness of painful tooth pulp stimulation. Science. 1979;203:1261-1263.
18. Lenz F, Gracely R, Romanoski A, et al. Stimulation in the somatosensory thalamus can reproduce both the aective and sensory dimensions of previously experienced pain. Nat Med. 1995;1:910-913.
19. Lenz FA, Gracely RH, Hope EJ, et al. e sensation of angina can be evoked by stimulation of the human thalamus. Pain. 1994;59:119-125.
20. Saal JSM. General principles of diagnostic testing as related to painful lumbar spine disorders—a critical appraisal of current diagnostic techniques. Spine. 2002;27:2538-2545.
21. Carragee EJ. Psychological screening in the surgical treatment of lumbar disc herniation. Clin J Pain. 2001;17:215-219.
22. North R, Kidd D, Zahurak M, et al. Specicity of diagnostic nerve blocks: a prospective, randomized study of sciatica due to lumbosacral spine disease. Pain. 1996;65:77-85.
SECTION
II
314 DIAGNOSIS
23. O’Neill C, Kurgansky M. Subgroups of positive discs on discography. Spine. 2004;29:2134-2139.
24. Handwerker HO, Kobal G. Psychophysiology of experimentally induced pain. Physiol Rev. 1993;73:639-671.
25. Rhudy JL, Meagher MW. Fear and anxiety: divergent eects on human pain thresholds. Pain. 2000;84:65-75.
26. Carragee E, Tanner C, Vittum D, et al. Positive provocative
discography as a misleading nding in the evaluation of low back pain. Proceedings of the North American Spine Society, 1997,
p 388.
27. Sackett D, Haynes R. Evidence base of clinical diagnosis: the architecture of diagnostic research. BMJ. 2002;324:539-541.
28. Schwarzer A, Wang S, Bogduk N, et al. Prevalence and clinical features of lumbar zygapophysial joint pain: a study in an Australian population with chronic low back pain. Ann Rheum Dis. 1995;54:100-106.
29. Schwarzer AC, Aprill CN, Derby R, et al. e false-positive rate of uncontrolled diagnostic blocks of the lumbar zygapophysial joints. Pain. 1994;58:195-200.
30. Block A, Vanharanta H, Ohnmeiss D, et al. Discographic pain report: inuence of psychological factors. Spine. 1996;21:
334-338.
31. Ohnmeiss DD, Vanharanta H, Guyer RD. e association between pain drawings and computed tomographic/ discographic pain responses. Spine. 1995;20:729-733.
32. Schellhas KP, Pollei SR, Dorwart RH. oracic discography: a safe and reliable technique. Spine. 1994;19:2103-2109.
33. Nordin M, Carragee EJ, Hogg-Johnson S, et al. Assessment of neck pain and its associated disorders. Results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Spine. 2008;33:S101-S122.
34. Heggeness MH, Watters WC III, Gray PM Jr. Discography of lumbar discs aer surgical treatment for disc herniation. Spine.
1997;22:1606-1609.
35. Carragee EJ, Chen Y, Tanner CM, et al. Provocative discography in patients aer limited lumbar discectomy: a controlled, randomized study of pain response in symptomatic and asymptomatic subjects. Spine. 2000;25:3065-3071.
36. Derby R, Kim B-J, Lee S-H, et al. Comparison of discographic
ndings in asymptomatic subject discs and the negative discs of chronic LBP patients: can discography distinguish asymptomatic discs among morphologically abnormal discs? Spine J. 2005;5:389-394.
37. Carragee EJ, Alamin TF, Miller J, et al. Provocative discography in volunteer subjects with mild persistent low back pain. Spine J. 2002;2:25-34.
38. Carragee EJ, Alamin TF, Parmar V, et al. Low pressure positive discography in subjects asymptomatic of signicant LBP
illness. Spine. 2006;31:505-509.
39. Cohen SP, Hurley RW. e ability of diagnostic spinal injections to predict surgical outcomes. Anesth Analg. 2007;105:1756-1775.
40. Colhoun E, McCall IW, Williams L, et al. Provocation discography as a guide to planning operations on the spine. J Bone Joint Surg Br. 1988;70:267-271.
41. Madan S, Gundanna M, Harley JM, et al. Does provocative discography screening of discogenic back pain improve surgical outcome? J Spinal Disord Tech. 2002;15:245-251.
42. Ohtori S, Kinoshita T, Yamashita M, et al. Results of surgery for discogenic low back pain: a randomized study using discography versus discoblock for diagnosis. Spine. 2009;34: 1345-1348.
43. Carragee EJ, Lincoln T, Parmar VS, et al. A gold standard evaluation of the “discogenic pain” diagnosis as determined by provocative discography. Spine. 2006;31:2115-2123.
44. Freeman BJ, Fraser RD, Cain CM, et al. A randomized, double-blind, controlled trial: intradiscal electrothermal therapy versus placebo for the treatment of chronic discogenic low back pain. Spine. 2005;30:2369-2377.
45. Pauza KJ, Howell S, Dreyfuss P, et al. A randomized, placebo-
controlled trial of intradiscal electrothermal therapy for the treatment of discogenic low back pain. Spine. 2004;4:27-35.
46. Derby R, Lettice JJ, Kula TA, et al. Single-level lumbar fusion in chronic discogenic low-back pain: psychological and emotional status as a predictor of outcome measured using the 36-item Short Form. J Neurosurg Spine. 2005;3:255-261.
47. Carragee EJ, Chen Y, Tanner CM, et al. Can discography cause long-term back symptoms in previously asymptomatic subjects? Spine. 2000;25:1803-1808.
48. Korecki CL, Costi JJ, Iatridis JC. Needle puncture injury aects intervertebral disc mechanics and biology in an organ culture model. Spine. 2008;33:235-241.
49. Nassr A, Lee JY, Bashir RS, et al. Does incorrect level needle localization during anterior cervical discectomy and fusion lead to accelerated disc degeneration? Spine. 2009;34:189-192.
50. Carragee EJ, Don AS, Hurwitz EL, et al. Does discography cause accelerated progression of degeneration changes in the lumbar disc: a ten-year matched cohort study. Spine. 2009;34: 2338-2345.
51. Cuellar JM, Stau MP, Herzog RJ, et al. Does provocative discography cause clinically important injury to the lumbar intervertebral disc? A 10-year matched cohort study. Spine J. 2016;16(3):273-280.
III
SECTION
SURGICAL ANATOMY AND APPROACHES
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SECTION
18
Cervical Spine: Surgical Approaches
CHAPTER
e cervical spine is a complex structure with many sensitive anatomic elements. Successful surgical manipulation of the cervical spine requires an in-depth understanding of how vascular, neural, and musculoskeletal elements interweave in order to prevent dire complications. is chapter rst exam-
ines the anatomy of the cervical spine, focusing on surface anatomy, osseous anatomy, bony articulations, ligaments, intervertebral discs, neurovascular structures, musculature, and triangles of the cervical spine. In the second section, the applied surgical anatomy is explored, with descriptions of both anterior and posterior approaches to the cervical spine.

Surgical Anatomy

Surface Anatomy and Skin
Surface landmarks are the key to successful localization of specic vertebral levels. For example, prominent musculoskel­etal structures—namely, the hyoid bone, thyroid cartilage, and cricoid cartilage—delineate C3, C4, and C6, respectively.1 e
transverse processes can generally be palpated, with the trans­verse process of the atlas prominently featured anterior and inferior to the mastoid process. e Chassaignac tubercle, the anterior prominence of the transverse process of C6, is another important landmark that can be palpated. When palpating in a cranial-to-caudal direction along the posterior midline, the spinous process of the second vertebra is the rst bony promi-
nence that can be felt. Due to the natural lordosis of the cervi­cal spine, the next palpable spinous process is typically of the sixth or seventh vertebra, with the seventh vertebra being particularly prominent.
When considering anterior approaches, surgical incisions should fall in line with skin creases to facilitate healing and prevent more noticeable scarring. In the lower neck, skin creases are transverse. Moving cranially, skin creases become more oblique in orientation. Skin on the front of the neck is generally soer, more mobile, and well vascularized, in con-
trast to skin on the back of the neck. As such, the typical longitudinal midline skin incision used on the posterior neck results in increased scar formation because of trapezius muscle tension.
Hamid Hassanzadeh
Varun Puvanesarajah
Howard S. An
Osseous Anatomy and Bony Articulation
e cervical spine comprises the rst seven vertebrae in the spinal column. e bony anatomy and articulations of the
upper cervical spine (occiput–C1–C2) are unique and distinct from the remaining lower ve cervical vertebrae (C3–C7).
e atlas, or C1, is a ringlike structure lacking a body and a spinous process. It consists of two thick lateral masses plus an anterior and posterior arch. e longus colli muscle and anterior longitudinal ligament attach to the anterior tubercle of the atlas, whereas the posterior tubercle serves as the bony attachments for the rectus minor muscle and suboc­cipital membrane. e superior and inferior oblique muscles attach to the large transverse processes. e vertebral artery passes through the foramen transversarium located within the transverse process and courses posteriorly within a sulcus on the superior aspect of the posterior arch of the atlas. In 15% of the population, the sulcus for the vertebral artery can be completely covered by an anomalous ossication, which
has been called the ponticulus posticus and may have surgical implications when identifying anatomic landmarks for bony xation of C1.
e axis, or C2, is characterized by an odontoid process, or dens, that projects upward anteriorly, articulating with the posterior aspect of the anterior arch of the atlas as a synovial joint. At its narrowest portion, at the base of the dens, the coronal and sagittal plane diameters are 8 to 10 mm and 10 to 11 mm. bid spinous process, which serve as attachments for the rectus major and inferior oblique muscles. e zone between the lamina and the lateral mass of the axis is indistinct, and posteriorly the neural arch connects to the body by large pedicles that are 8 mm wide and 10 mm long.5 Lying directly anterolateral to the pedicle is the vertebral artery, which runs through the foramen transversarium. e pedicle of the axis projects 30 degrees medially and 20 degrees superiorly from a posterior-to-anterior direction.
e bony articulations of the upper cervical spine (occiput– C1–C2) are unique and warrant special attention (Fig. 18.1). e atlanto-occipital articulation is a shallow ball-and-socket joint allowing for considerable motion mostly in exion, extension, and lateral bending. e greatest degree of exion
2
3,4
Posteriorly, the axis has a large lamina and a
4
III
317
318 SURGICAL ANATOMY AND APPROACHES
O
A
FIG. 18.1 Coronal cryomicrotome section of the upper cervical spine. Note
articulation between occiput (O) and atlas (A). The atlantoaxial joint is
identied by the arrow.
and extension of any cervical articulation occurs at this level (25 degrees).6 Lateral displacement is minimized because the lateral wall of the cup-shaped articulation of the atlas is higher than the medial wall. e superior articular surface of the atlas
projects cephalad and medially, articulating with the occipital condyle, which projects caudad and laterally. Conversely, the inferior articular surface of the atlas projects caudad and medially and articulates with the laterally projecting superior facet of the axis. As a result of this bony conguration, axial
loads on the atlas tend to result in horizontal displacement of the lateral masses.
7
e atlantoaxial articulation provides about 50% of rota-
tory motion of the cervical spine.
6,8
e transverse ligament, which spans across the arch of the atlas, holds the odontoid process against the anterior arch of the atlas, creating a pivot joint with a synovial membrane and capsular ligaments ante­riorly and posteriorly to the dens. is transverse ligament is the principal stabilizing structure for the atlantoaxial articula­tion and averages 21.9 mm in length.9 e transverse ligament has superior and inferior extensions, which form the cruciform ligament of the atlas, connecting it to the anterior edge of the foramen magnum and posterior aspect of the C2 body. To allow more rotatory motion, the inferior facets of the atlas are
atter and more circular than the superior facets, and face inferiorly to articulate with the axis.
e lower cervical vertebrae are morphologically similar and increase in dimension as they proceed inferiorly from C3 to C6, with C7 as the transitional vertebra into the tho­racic spine. e vertebral bodies are small and oval, with the mediolateral diameter greater than the anteroposterior diameter.
e inferior surface of the vertebral body is convex in the coronal plane and concave in the sagittal plane, with the anterior lip occasionally overlapping the inferior vertebra.9 Conversely, the superior surface of the vertebral body is convex or straight in the sagittal plane and concave in the coronal plane, creating projections on either side of the lateral superior
surface, called the uncus, or hook. ese processes project upward and conform to small grooves in the inferolateral border of the cephalad vertebra, forming the uncovertebral joints, or joints of Luschka. e width and depth of the verte­bral surfaces average 17 mm and 15 mm from C2 to C6 and increase to about 20 mm and 17 mm at C7. Vertebral heights on the posterior wall in the mid-sagittal plane range from 11 to 13 mm.
10
e pedicles project posterolaterally from the vertebral body and join the lamina to form the vertebral arch. From C3 to C7, the angulation of the pedicles varies from 8 degrees below to 11 degrees above the transverse plane, and decreases from 45 degrees to 30 degrees in relation to the sagittal plane.10 e width and height of the pedicles increase slightly in size from C3 to C7, and average diameters are 5 to 6 mm and 7 mm. e lateral wall of the pedicle is thinner than the medial wall and should be taken into consideration if attempts at pedicle xation are considered in this region.
11–13
At the junction of the pedicle and lamina, the anterior tubercle of the transverse process projects laterally and is con­nected to the posterior tubercle by the costotransverse lamella (bar), creating the foramen transversarium. Passing through the foramen transversarium is the vertebral artery and venous system.
In the lower cervical spine, the neural foramina are bounded anteriorly by the uncinate process, the posterolateral aspect of the intervertebral disc, and the inferior portion of the vertebral body; posteriorly by the facet joint and superior articular process of the vertebral body below; and superiorly and inferiorly by adjacent pedicles. Vertebral notches located on the superior and inferior aspect of each pedicle contribute to the size of the neural foramina, which are 9 to 12 mm in height, 4 to 6 mm in width, and 4 to 6 mm in length, and are aligned 45 degrees to the sagittal plane.
14,15
ey can be visual-
ized radiographically with oblique views, with the right neural foramina outlined on the le posterior oblique view and the
le neural foramina outlined on the right posterior oblique view.
e spinal canal is triangular and at all levels in the cervical spine is signicantly greater in the medial-to-lateral dimen- sion than in the anterior-to-posterior dimension. e cross­sectional area of the spinal canal is largest at C2 and smallest at C7, with a sagittal diameter of about 23 mm at C1 and 20 mm at C2, decreasing to 17 to 18 mm at C3–C6 and to 15 mm at C7.8 is is one reason that the passage of sublami­nar wires is safer in the upper cervical spine than in the lower cervical spine.
e lateral mass, an important structure for posterior cervical plate-screw systems, forms at the junction of the lamina and the pedicle and gives rise to the superior and inferior articular processes. ese processes project upward and downward and are angled approximately 45 degrees cephalad from the transverse plane, gradually assuming a more vertical position as they descend into the thoracic region (Fig. 18.2). e articular process of the superior facet faces posteriorly, whereas the inferior facet of the upper vertebra faces anteriorly; the facets oppose one another to form a zygapophyseal joint. e facet joints are true diarthrodial
Chapter 18 Cervical Spine: Surgical Approaches 319
O
T
SECTION
C5
C6
C7
FIG. 18.2 Parasagittal cryomicrotome section of facet joints. The lateral
mass of C7 is more elongated from superior to inferior and thinner from anterior to posterior. The facet joint angle is roughly 45 degrees from the transverse plane and assumes a more vertical position distally.
joints, with articular cartilage and menisci surrounded by a brous capsule lined by a synovial membrane. e interfacet distances are relatively constant between levels, with individual variations ranging from 9 to 16 mm (average, 13 mm).
5,16
Posteriorly, the spinous processes project inferiorly and are
bid from C3 to C6; the C7 spinous process is large and not bid, and is oen called the vertebra prominens. e junction between the spinous process and lamina, the spinolaminar line, is an important anatomic landmark during spinous process wiring. Inadvertent penetration of the wire anterior to this line may result in spinal cord impingement.
e cervicothoracic junction is a transition region, with C7 having similar anatomic characteristics as T1 and T2. e dimensions of the vertebral body and the sizes of the trans­verse processes and spinous processes are larger at C6 and C7. Additionally, dimensions of the spinal canal decrease at C6 and C7, representing a distinct transition to the thoracic region. e articulating facet joint between C7 and T1 resembles the thoracic facet joint, and the lateral mass of C7 is thinner than that of upper levels. Morphologic characteris­tics of pedicles of C7, T1, and T2 were obtained with respect to diameters, depths, and medial angulations. Inner diameters of the pedicles at C7, T1, and T2 from medial to lateral plane averaged 5.2, 6.3, and 5.5 mm. Medial angulations were 34, 30, and 26 degrees at C7, T1, and T2, respectively.
10,17
ese morphologic characteristics should be remembered when performing transpedicular procedures in the cervicothoracic region.
S
FIG. 18.3 Midsagittal microtome section at the upper cervical spine. The
transverse ligament (T ) acts as a stabilizer of the atlantoaxial joint by helping to restrain the odontoid (O) from posterior translation. The spinal cord (S), ligamentum avum (L), and posterior arch of atlas (A) are also
identied.
A
L
Ligaments
In addition to the bony anatomy, the ligamentous attachments provide support to the cervical spine and associated articula­tions. In the atlanto-occipital complex, two membranous attachments, the anterior and posterior atlanto-occipital membranes, connect the anterior and posterior arch of C1 to the margins of the foramen magnum. e anterior atlanto-
occipital membrane is the superior continuation of the anterior longitudinal ligament, whereas the posterior membrane is the superior continuation of the ligamentum avum.
e transverse ligament is the major stabilizer of the atlan­toaxial complex (Fig. 18.3). It attaches laterally to tubercles located on the posterior aspect of the anterior arch of C1, where it blends with the lateral mass. Secondary stabilizers include the thick alar ligament, which arises from the sides of the dens to the medial aspects of the condyles of the occipital bone, and the apical ligament, which arises from the apex of the dens to the anterior edge of the foramen magnum. In some individuals, an anterior atlantodental ligament exists connect­ing the base of the dens to the anterior arch of the atlas.18 e tectorial membrane, the superior continuation of the posterior longitudinal ligament, covers the dens and all the occipitoaxial ligaments and extends from the posterior body of C2 to the basilar portion of the occipital bone and the anterior aspect of the foramen magnum.
e bodies of the lower cervical vertebrae (C3–C7) are connected by two longitudinal ligaments and the interverte­bral discs. e anterior longitudinal ligament is a strong band that attaches from the skull, as the anterior atlanto-occipital membrane, and continues caudad over the entire length of the spine down to the sacrum. e anterior longitudinal ligament is thinner and more closely attached at the intervertebral disc margins than at the anterior vertebral surfaces.19 e anterior longitudinal ligament also sweeps around and envelops the lateral aspect of the vertebral bodies under the longus colli
III
320 SURGICAL ANATOMY AND APPROACHES
muscle, and the lateral extension is continuous with the deep layer of the posterior longitudinal ligament in the region of the intervertebral foramina.
e posterior longitudinal ligament, lying within the ver­tebral canal on the posterior aspect of the vertebral body and intervertebral disc, is wider in the upper cervical spine than the lower cervical spine.19 Superiorly, it is continuous with the tectorial membrane; as it descends, it widens over the inter­vertebral discs and narrows behind each vertebral body. e posterior longitudinal ligament supplies additional strength and stability to the posteromedial bers of the anulus. ere is an area of relative weakness in the posterolateral corners of the disc, however, at the junction of the posterior longitudinal ligament and uncinate process. As a result, it is the site of most cervical disc herniations.20 According to Hayashi and col­leagues,21 the posterior longitudinal ligament is double-layered, and the deep layer sends bers to the anulus brosus and continues laterally to the region of the intervertebral foramina. e supercial or more dorsal layer of the posterior longitu­dinal ligament is adjacent to the dura mater and continues as a connective tissue membrane, which envelops the dura mater, nerve roots, and vertebral artery, suggesting that this mem­brane may serve as a protective barrier.
e ligamentum avum of the cervical spine attaches to the anterior surface of the lamina above and to the superior margin of the lamina below and extends laterally to the articu­lar processes, contributing to the boundary of the interverte­bral foramen. e ligamentum avum consists primarily of elastic bers, whose numbers lessen with aging, resulting in anterior buckling that can contribute to symptoms of spinal cord compression. A gap in the midline of the ligamentum avum allows for the exit of veins.
e interspinous ligament of the cervical spine is thin and less well developed than in the lumbar region. It attaches in an oblique orientation from the posterosuperior aspect to the anteroinferior aspect of the spinous process. ere is no separate supraspinous ligament in the cervical region. e ligamentum nuchae, a broelastic septum, is the superior con­tinuation of the supraspinous ligament of the thoracolumbar spine and extends from the external occipital protuberance to C7.
and posterior longitudinal ligaments and are rmly attached to the adjacent vertebral endplates. e bers of the lamella run perpendicular to the bers of the adjacent lamella. e collagen bers in the posterior portion of the disc run more vertical than oblique; this may account for the relative fre­quency of radial tears seen clinically. e discs are shaped to
conform to the surface of the bodies; the superior surface of the disc is concave, and the inferior surface of the disc is correspondingly convex in the coronal plane. e discs are also slightly thicker anteriorly than posteriorly, which contrib­utes to the lordotic posture of the cervical spine. e cervical intervertebral discs allow some translational movement in the sagittal plane, but the uncinate processes resist lateral move­ment. e uncinate process, located in the posterolateral aspect of the disc, also helps prevent disc herniations in this area. Degeneration of the anulus brosus (Fig. 18.4) in the
cervical region is similar to the lumbar region in that concen­tric, transverse, and radial tears of the anulus occur, and the radial tear in the posterior aspect of the disc may be more clinically signicant.
e cartilaginous endplate is a layer of hyaline cartilage resting on the subchondral bone and serves as a barrier between the pressure of the nucleus pulposus and the adjacent vertebral bodies. is cartilage is a growth plate and respon­sible for endochondral ossication during growth (Fig. 18.5). e cartilaginous endplates also allow the insertion of the inner bers of the anulus brosus and the diusion of nutri-
ents from the subchondral bone to the disc.
Intervertebral Discs
Intervertebral discs are present between all vertebrae except at the atlantoaxial level. Each intervertebral disc is an avascular structure that consists of the nucleus pulposus at the interior of the disc, the outer anulus brosus, and the cartilaginous endplates adjacent to the vertebral surfaces. e nucleus pul­posus functions as a shock absorber, and the anulus brosus maintains the stability of the motion segment. With increasing age, the margin between the nucleus pulposus and anulus brosus becomes less distinct. Oen, by age 50 years, the nucleus pulposus has become a brocartilaginous mass similar to the inner zone of the anulus brosus.
e anulus has an outer collagenous layer, in which the bers are arranged in oblique layers of lamellae. e outermost bers of the anulus brosus are contiguous with the anterior
22
FIG. 18.4 Midsagittal cryomicrotome section of a degenerative cervical
spine showing degeneration of anulus brosus and herniation of nucleus pulposus posteriorly with impingement of the spinal cord.
Chapter 18 Cervical Spine: Surgical Approaches 321
a
n
FIG. 18.5 Midsagittal microtome section of the cervical spine showing
nucleus pulposus (n) and outer anulus brosus (a) of the intervertebral disc. Arrows identify a cartilaginous endplate.
Neural Elements
e cervical cord emerges from the foramen magnum as a continuation of the medulla oblongata. ere is considerable variation in size of the spinal cord; however, in general, owing to the increased nerve supply to the upper limbs, the cervical cord enlarges from C3 and becomes maximal at C6. Maximal transverse diameters of 13 to 14 mm have been reported,23 with transverse areas ranging from 58.3 ± 6.7 mm3 at C624 to
85.8 ± 7.2 mm3 at C4–C5. e spinal cord includes the outer white matter and the
inner gray matter. e white matter of the spinal cord contains nerve bers and glia, and is divided into the posterior, lateral, and anterior columns. e posterior column includes the fasciculus cuneatus laterally and fasciculus gracilis medially, mediating proprioceptive, vibratory, and tactile sensations. e lateral column contains the descending motor lateral corticospinal and lateral spinothalamic fasciculi. e anterior funiculus contains the ascending anterior spinothalamic tract and other descending tracts. e lateral spinothalamic tracts cross through the ventral commissure to the contralateral side of the cord, conveying pain and temperature sensations. e anterior spinothalamic tract conveys the crude touch sensation.
e gray matter of the spinal cord contains cell bodies
of eerent and internuncial neurons. e somatosensory
neurons are located in the posterior horn, and the somato­motor neurons are found in the anterior horn of the gray matter. e visceral center of the gray matter is found in the intermediolateral horn. In the center of the spinal cord is the central ependymal canal for the passage of cerebrospinal uid.
25
e spinal cord is covered by the pia mater, which is the
outer lining of the cord, and transparent arachnoid membrane that contains the cerebrospinal uid. e dura mater is the outer covering of the spinal cord, which becomes the inner layer of the cranial dura at the level of the foramen magnum. e cervical cord is anchored to the dura by the dentate liga­ments that project laterally from the lateral side of the cord to the arachnoid and dura at points midway between exiting spinal nerves. By suspending the spinal cord in the cerebro­spinal uid, the dentate ligaments cushion and protect the
cord, while minimizing the movement of the cord during range of motion (ROM). e epidural space contains fat,
internal vertebral venous plexus, and loose connective tissue. is venous plexus may be involved in spreading infection or neoplasm. ere is a potential space between the dura and the arachnoid, and the subarachnoid space is between the arach­noid and the pia. e subarachnoid space contains the cere­brospinal uid (CSF), spinal blood vessels, and nerve rootlets
from the spinal cord.
e dorsal sensory rootlets enter the cord through the lateral longitudinal sulcus, and the ventral motor rootlets exit the cord through the ventral lateral sulcus. e six or eight rootlets at each level leave the spinal cord laterally to lie in the lateral subarachnoid space bathed in the CSF. e rootlets join to form the dorsal and ventral root, which together enter a narrow sleeve of arachnoid and pass through the dura to become a nerve root at each level. e cervical nerve roots that form from the ventral and dorsal nerve rootlet extend anterolaterally at a 45-degree angle to the coronal plane and inferiorly at about 10 degrees to the axial plane.15 e nerve roots enter the intervertebral foramina by passing directly lat­erally from the spinal canal adjacent to the corresponding disc and over the top of the corresponding pedicle. e anterior root lies anteroinferiorly adjacent to the uncovertebral joint; the posterior root is close to the superior articular process. e nerve root is positioned at the tip of the superior articular process in the medial aspect of the neural foramen; it courses more inferiorly to position over the pedicle in the lateral aspect of the neural foramen (Fig. 18.6).
e roots occupy about one-third of the foraminal space in the normal spine but much more in the degenerative spine. e roots are located in the inferior half of the neural foramen normally, but the nerve roots occupy a more cranial part of the foramina, and the size of the foramen is diminished if the neck is fully extended.26 e upper half of the neural foramen contains fat and small veins.27 e nerve root is enlarged in the distal aspect of the intervertebral foramen, and the dorsal root ganglion is located just distal to the foramen.28 e dorsal root ganglion is located between the vertebral artery and a small concavity in the superior articular process. Just distal to the ganglion and outside the intervertebral foramen, the anterior and posterior roots join to form the spinal nerve. e spinal nerve divides into dorsal and ventral primary rami branches.
e gray rami from the sympathetic cervical ganglion join the ventral primary rami. ere are interconnections between gray rami, the perivascular plexus around the vertebral artery, and the sympathetic trunk, all of which give contributions
SECTION
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322 SURGICAL ANATOMY AND APPROACHES
FIG. 18.6 Parasagittal cryomicrotome section of the lateral aspect of the
neural foramen shows a nerve root coursing more inferiorly lying over a pedicle as it begins to exit the foramen.
e second cervical nerve lies on the lamina of the axis posterior to the lateral mass; the posterior primary ramus or the greater occipital nerve pierces the trapezius about 2 cm below the external occipital protuberance and 2 to 4 cm from the midline. Trauma or irritation to any of the three terminal nerves (the greater and lesser occipital nerve and the greater auricular nerve) can produce pain, headache, or hyperesthesia in their dermal distribution over the occiput and around the ear.
Cutaneous branches of the posterior primary rami of C2– C5 are consistently present in the skin of the nuchal region; the largest cutaneous nerve in this region is the greater occipi­tal nerve. e lesser occipital nerve is a branch from the anterior cervical plexus, running upward and lateral to the greater occipital nerve. e posterior primary ramus of C3, or the third occipital nerve, pierces the trapezius more inferiorly and about 1 cm medial from the midline. e cervical nerve exits over the pedicle that bears the same number except the C8 cervical nerve lies between the C7 and T1 vertebrae. e posterior primary rami of cervical nerves send motor bers to
the deep muscles and sensory bers to the skin, but the rst cervical nerve has no cutaneous branches. e anterior
primary rami of C1–C4 form the cervical plexus, and the rami of C5–T1 form the brachial plexus.
Vascular Structures
to the ventral nerve plexus to innervate the anterior longitu­dinal ligament, outer anulus brosus, and anterior vertebral
29,30
body.
e dorsal nerve plexus receives contributions from the sinuvertebral nerves, which originate from the gray rami and perivascular plexus of the vertebral artery. e dorsal nerve plexus innervates the posterior longitudinal ligament, and the sinuvertebral nerves give branches to the posterior part of the anulus and the ventral part of the dura. e sinuvertebral nerves innervate two or more discs or motion segments.
e rst cervical nerve or suboccipital nerve exits the
vertebral canal above the posterior arch of the atlas and pos­teromedial to the lateral mass, and lies between the vertebral artery and the posterior arch. e posterior primary ramus of the rst cervical nerve enters the suboccipital triangle and sends motor bers to the deep muscles. e anterior primary ramus of the rst cervical nerve forms a loop with the second anterior primary ramus and sends bers to the hypoglossal nerve. e cervical plexus receives bers from anterior primary rami of C1–C4. e cervical plexus is located
opposite C1–C3, ventral and lateral to the levator scapulae and middle scalene muscles. e cervical plexus has distributions to the skin and muscles, such as the rectus capitis anterior and lateralis, longus capitis and cervicis, levator scapulae, and middle scalene. e cervical plexus forms loops and branches to supply the sternocleidomastoid and trapezius muscles. It has communications with the hypoglossal nerve from C1 and C2, and leaves this trunk as the superior root of the ansa cervicalis, which is a nerve loop that is formed with the inferior root from C2 and C3.
e major blood supply of the cervical cord and cervical spine is the vertebral artery. Variations of the course of the vertebral artery have been reported.31 In most cases, the vertebral artery originates from the rst part of the subclavian artery and
begins its ascent behind the common carotid artery between the longus colli and the anterior scalene. In the lower cervical spine, the vertebral arteries are crossed by the inferior thyroid artery and on the le by the thoracic duct. e vertebral arter-
ies course anterior to the ventral rami of the seventh and eighth cervical nerves and the C7 transverse process before entering the C6 transverse foramen, where they ascend within the transverse foramen of C6–C2.
e surgeon should remember that the vertebral artery is located lateral to the uncinate process and in line with the middle one-third of the vertebral body just anterior to the nerve root. During anterior exposure of the vertebral body and intervertebral discs, too far lateral dissection on the inferior half of the vertebral body and uncovertebral joints would endanger the vertebral artery and spinal nerve around the intervertebral foramen. e vertebral artery may also be involved in patients with severe cervical spondylosis when it may be impinged by the osteophyte. At the level of the atlas, the artery winds posteromedially around the lateral mass and over the posterior arch of the atlas before passing through the posterior atlanto-occipital membrane into the foramen magnum, joining the other vertebral artery to form the basilar ar t er y.
In the foramen magnum region, the vertebral artery gives branches anteriorly that join to form the single anterior spinal artery, whereas the paired posterior spinal arteries are branches from the posterior inferior cerebellar arteries. e anterior