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Chapter 13 Spine Imaging 213
SECTION
II
A
FIG. 13.16 Lumbar canal stenosis. (A) Sagittal and (B) axial T2-weighted magnetic resonance images show
severe central canal stenosis at L3–L4 and L4–L5 with marked compression of the thecal sac owing to anterior bulge of the anulus brosus and facet hypertrophic degenerative change. There are small bilateral facet
eusions (arrows).
B
spondylolisthesis are bilateral defects in the pars interarticu­laris (isthmic spondylolisthesis) and facet disease (degenera­tive spondylolisthesis). e degenerative variety is the most
common in older adults.
Because of its ability to obtain direct sagittal images free of overlapping structures and patient rotation, MRI is an accurate method of diagnosing spondylolisthesis. MRI is nearly always performed with the patient supine, however. In that position, a vertebra with subluxation can be normally aligned. A more accurate method of detecting listhesis is by weight-bearing lateral lumbar radiographs. e detection of spondylolysis (pars interarticularis defect without ventral slippage) by MRI can be problematic, and it is generally agreed that plain lms
and CT are more reliable for its diagnosis. Because MRI is being increasingly used as the rst and only imaging modality in evaluating patients with low back pain and radicular symp­toms, many cases of spondylolysis are imaged without the benet of correlative plain lms or CT studies.
166
Using MRI, sagittal T1-weighted images are best for showing the pars interarticularis owing to their higher signal-to-noise ratio, the depiction of the pars marrow as hyperintense, and the minimal obliquity of the pars in this imaging plane (Fig. 13.18). If the pars appears normal (i.e., contiguous normal marrow signal), one can be certain that it is intact.
167
Additionally, myelopathic symptoms tend to occur when the canal cross-sectional area is less than 60 mm2. e ratio of the anteroposterior canal diameter to the vertebral body diameter has been used to assess cervical stenosis. is Pavlov ratio (sometimes referred to as the Torg ratio) is normal if it is 1 or
168
gre ater.
A ratio of 0.8 or less is considered abnormal. As a ratio, however, it can be abnormal not only because of an abnormally small canal diameter (small numerator), but also because of an abnormally large vertebral body (large denomi­nator). is ratio method also does not take into account the size of the spinal cord itself. As an isolated tool, this method is of historical interest only and is useless in evaluating cervical spinal cord compression.
Takahashi and colleagues and others have described areas of increased signal intensity on T2-weighted images within the cervical cord owing to extradural compression, which vari­ously reects myelomalacia, gliosis, and demyelination and
edema (Fig. 13.19).
169
Patients who show areas of abnormal signal within the cord tend to have a worse clinical condition than patients with normal cord signal intensity. ese abnor­mal signal changes can disappear or diminish aer surgery to relieve the cord compression.

Postoperative Imaging

Cervical Radiculopathy and Myelopathy
Various studies have shown that canal size is reduced in patients with cervical spondylotic myelopathy. e normal
diameter of the canal from C3 to C7 is approximately 17 mm and can be decreased to 12 mm or less in cervical spondylotic myelopathy. e size that is associated with myelopathy has ranged, however, from less than 10 mm up to 14 mm.
Causes of early and delayed failure of surgery are listed in
Boxes 13.1 and 13.2. Caution must be used in interpretation
of CT, CT myelography, and MRI within the rst 6 weeks aer surgery owing to the large amount of tissue disruption and edema that may be present producing mass eect on the ante­rior thecal sac, even in the absence of any clinical symptoms. MRI may be used in the immediate postoperative period for a
214 DIAGNOSIS
A
C
FIG. 13.17 Synovial cyst. (A) Sagittal and (B) axial T1-weighted magnetic resonance images show mass with
central low signal centered on the right anterior facet that eaces the right dorsal aspect of the thecal sac. (C) Sagittal and (D) axial T2-weighted images show central high signal of uid consistent with synovial cyst.
BOX 13.1 Technical Causes of Early Spine Surgery Failure
Hematoma Infection Inadequate decompression of bony foraminal or central stenosis Insucient removal of herniation Neural trauma Unrecognized free disc fragment Wrong level surgery
B
D
BOX 13.2 Technical Causes of Delayed Recurrence of Low Back Pain or Radiculopathy
Arachnoiditis
Epidural brosis Facet arthropathy with foraminal stenosis Instability New or recurrent herniation Pseudomeningocele Central canal stenosis Infection
more gross view of the thecal sac and epidural space, to exclude signicant postoperative hemorrhage, pseudomeningocele, or disc space infection at the laminectomy site. CT myelography is also a direct way to dene a pseudomeningocele and to image the spine when hardware is present (Fig. 13.20).
Small uid collections are commonly seen in the posterior tissues aer laminectomy. e signal intensities can vary depending on whether the collections are serous (follow CSF
signal intensity) or serosanguineous (increased signal on T1-weighted images owing to hemoglobin breakdown prod­ucts). e distinction between small postoperative uid col-
lections and infected collections cannot be made by MRI morphology or signal intensity. Acute hemorrhage typically shows isointense to increased signal in the epidural space on T1-weighted images and should show diminished signal on
Chapter 13 Spine Imaging 215
gradient-echo or T2-weighted images. Very acute blood col­lections may be isointense, however, on T1-weighted and T2-weighted images (Fig. 13.21).
Aside from the various options for instrumentation that are
available, dierent types of bone gra materials are available,
FIG. 13.18 Spondylolysis. Sagittal T1-weighted magnetic resonance image
shows disruption of cortical margin of pars interarticularis (arrow) at L5–S1 consistent with spondylolysis. There is severe foraminal stenosis at L5–S1.
some with ramications when imaging.
170
Bone morphogenic protein (BMP) can produce imaging ndings that can be misinterpreted as infection, including prevertebral so tissue swelling and vertebral body endplate resorption, although these ndings typically resolve by 6 months.
171-173
Epidural Fibrosis and Disc Herniations
e use of contrast medium–enhanced MRI in the evaluation of scar versus disc has been examined by several authors, with reported accuracy rates of 96% to 100% for distinguishing scar from disc. of the normal epidural fat with postoperative brotic tissue, which is capable of binding the dura and nerve roots to the surrounding structures anteriorly and posteriorly. Epidural brosis is seen to enhance consistently immediately aer injection of contrast material (Fig. 13.22). is enhancement occurs regardless of the time since surgery. Disc material does not enhance on the early postinjection images owing to its lack of vascularity (Fig. 13.23). In cases with a mixture of scar and disc material, scar enhances but the disc material does not enhance on early postinjection images.
used in the evaluation of postoperative patients. Georgy et al. examined 25 patients with recurrent pain aer lumbar disc surgery with MRI to evaluate the usefulness of gadolinium­enhanced fat suppression imaging in patients with failed back surgery. e addition of fat suppression to enhanced T1-weighted images improved the visualization of enhancing scar in all cases, helped distinguish scar from recurrent herniated disc, and showed more clearly the relationship of scar to the nerve
174
Lumbar epidural brosis (scar) is a replacement
Selective fat suppression on T1-weighted images has been
175
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II
A
FIG. 13.19 Cervical spondylosis. (A) Sagittal T1- and (B) T2-weighted magnetic resonance images show solid
fusion at C6–C7 level with a small osteophyte. There is severe central stenosis of the disc and osteophyte complex and posterior ligamentous hypertrophy at C4–C5, C5–C6, and T1–T2 levels. There is myelomalacia within the cord seen as high signal intensity on the T2-weighted image at C4–C5 (arrow). (C) Axial gradient­echo image at C4–C5 conrms severity of central stenosis owing to broad-based disc and osteophyte.
B
C
216 DIAGNOSIS
roots and thecal sac. Overall there are conicting data as to whether epidural scar is associated or causative of symptoms following back surgery. e presence of scar did not correlate with symptoms in a study of 40 patients.
176
When epidural scar
is present in symptomatic patients undergoing reoperation,
it is associated with a poor outcome.
177
Others suggest that psychosocial factors rather than the presence of epidural scar correlate better with symptoms.
178
Stenosis
Bony stenosis has been implicated as a cause of failed back surgery in 60% of cases. Various mechanisms can lead to stenotic changes in the canal or foramina. eir signicance may vary, and many of these stenoses are not symptomatic. Examples of mechanisms are as follows:
1. Bony overgrowth aer facetectomy may compromise a
lateral recess.
2. Aer posterior fusion, there may be late overgrowth of
bone into the posterior or lateral canals.
3. Aer anterior fusion, bone may extend into the canal or
foramen.
4. e narrowing of the interspace aer discectomy may allow
sucient facet overriding to produce a decreased size of the lateral recesses or foramina.
5. Postoperative spondylolisthesis can produce focal stenosis.
Arachnoiditis
FIG. 13.20 Pseudomeningocele. Axial computed tomographic scan after
myelography shows metal artifact from prior pedicle screw xation. There is pooling of contrast medium around and dorsal to the hardware owing to a large pseudomeningocele (arrows).
Spinal MRI can identify the various characteristics of lumbar arachnoiditis, as can CT and myelography.
179-181
ese may be classied into three categories or patterns, which can be applied to MRI, CT, or myelography, although a mixture of patterns can occur in any one patient.
182
A
FIG. 13.21 Recurrent herniation mimicking blood. This patient underwent multilevel laminectomy and L3–L4
discectomy 3 weeks before examination. (A) Sagittal T1-weighted magnetic resonance image shows vague anterior epidural mass at L3 and extensive postoperative changes in dorsal epidural soft tissues. (B) Sagittal T2-weighted image shows L3 epidural mass to be of low signal, with eacement of anterior thecal sac. (C) After
contrast administration, sagittal T1-weighted image shows slight peripheral enhancement. Dierential diagnosis included acute blood (deoxyhemoglobin) and large recurrent herniation. Because of homogeneity of low signal and contiguity with disc space at L3–L4, recurrent herniation was favored. A large herniation was found at reoperation.
B
C
Chapter 13 Spine Imaging 217
SECTION
II
A
FIG. 13.22 Postoperative epidural scar. Axial T1-weighted magnetic resonance images (A) before and (B) after
contrast administration show diuse enhancement of tissue surrounding the right lateral aspect of the thecal sac (large arrow) and exiting the right S1 root (small arrow).
A B
B
C
D E
FIG. 13.23 Recurrent herniation. (A) Sagittal T1-weighted magnetic resonance image shows large anterior
epidural mass extending dorsal to L4 body from L4–L5 disc space. The patient previously underwent L4 laminectomy and discectomy. (B) Sagittal T2-weighted image shows a large disc extrusion migrating superiorly from the disc space level, reecting free fragment. (C) After contrast medium administration, sagittal
T1-weighted image shows typical peripheral enhancement of large herniation. Axial T1-weighted images (D) before and (E) after contrast administration show peripheral enhancement of the disc component at mid-L4 level (arrow).
218 DIAGNOSIS
e rst pattern is central adhesion of the nerve roots within the thecal sac into a central clump of so tissue signal. Instead of showing their normal feathery pattern, the nerve roots are clumped into one or more cords. is pattern is most easily identied on axial CT myelography or T1-weighted MRI. e second pattern is adhesion of the nerve roots to the meninges, giving rise to an “empty thecal sac” sign. On MRI, only the homogeneous signal of the CSF is present within the thecal sac, and the nerve roots are peripherally attached to the meninges. On CT myelography, only the high-attenuation contrast agent within the thecal sac is visualized, without the nerve roots. In the third pattern, which can be viewed as an end stage of the inammatory response, the arachnoid becomes an inammatory mass that lls the thecal sac. On myelography, this type of arachnoiditis gives rise to a block, with an irregular “candle dripping” appearance. MRI shows a nonspecic so tissue mass, as does CT myelography.

Infection

Infection should be considered in the dierential diagnosis for back pain even though it is an uncommon disorder (1% of all cases of osteomyelitis). When infection is considered, accurate imaging is a necessary prelude for microbiologic diagnosis or surgical drainage. Because abnormalities that appear on plain radiographs usually take days to weeks to become apparent, radionuclide studies and MRI have been the primary imaging modalities for diagnosis of vertebral osteomyelitis.
CT has played a minor diagnostic role in cases with bony or so tissue components and is not considered a mainstay for the diagnosis of disc space infection. tive than either plain lms or CT for detecting vertebral osteomyelitis, and it approaches or equals the sensitivity of radionuclide studies (Figs. 13.24 and 13.25).
183,184
MRI is more sensi-
185,186
A
D
B
FIG. 13.24 Pyogenic disc space infection. (A) Sagittal T1-weighted
magnetic resonance image shows typical pattern of disc space infection with low signal from adjacent L3 and L4 bodies and abnormal morphology to the disc itself. There is kyphotic angulation at that level, with increased anterior epidural soft tissue. (B) Sagittal T2-weighted image shows abnormal increased signal from L3 and L4, with irregular margins to the disc space. There is severe thecal sac compromise (arrow). (C) Sagittal T1-weighted image after contrast administration shows marked enhancement of vertebral bodies, disc space, and epidural phlegmon. (D) Degree of thecal sac compromise (large arrow)
and diuse paravertebral extension of inammatory process (small arrows) are shown on axial T1-weighted image.
C
Chapter 13 Spine Imaging 219
SECTION
II
A
E
B
FIG. 13.25 Early disc space infection. (A) Sagittal T1-weighted magnetic resonance image shows loss of disc
space height at L2–L3 through L4–L5 but no overt marrow signal abnormality. (B) Sagittal T2-weighted image shows abnormal increased signal in L4–L5 disc space but no marrow signal abnormality. (C) Sagittal T1-weighted image after contrast administration shows mild patchy L4–L5 disc enhancement and mild endplate enhancement. Dierential diagnosis at this time is severe degenerative disc disease versus early
disc space infection. (D) Grossly abnormal signal involving L4 and L5 bodies with loss of disc margin was visible 5 weeks later on T1-weighted image. (E) L4–L5 disc now shows more marked increased signal on T2-weighted image.
C
D
It is imperative to obtain both T1- and T2-weighted images in the sagittal plane for optimal sensitivity to detect disease. e T1-weighted spin-echo image allows detection of the increased water content or marrow uid seen with inamma­tory exudate or edema. Similar to most pathologic processes, disc space infection or vertebral osteomyelitis results in increased signal intensity on T2-weighted images. e diag­nostic specicity of MRI is provided by the signal intensity changes on T1- and T2-weighted images and by the anatomic pattern of disease involvement and the appropriate clinical situation.
On T2-weighted images, the normal intervertebral disc usually shows increased signal intensity within its central portion that is bisected by a thin horizontal line of decreased
signal, termed the intranuclear cle. Aer the age of 30 years, the cle is almost a constant feature of normal intervertebral discs. Disc space infections on MRI typically produce conuent
decreased signal intensity of the adjacent vertebral bodies and the involved intervertebral disc space on T1-weighted images compared with the normal vertebral body marrow. A poorly dened endplate margin exists between the disc and adjacent vertebral bodies. T2-weighted images show increased signal intensity of the vertebral bodies adjacent to the involved disc and an abnormal morphology and increased signal intensity from the disc itself, with absence of the normal intranuclear cle. ese MRI ndings are much more typical of pyogenic than of tuberculous osteomyelitis.
187
In a comparative study
of patients with suspected vertebral osteomyelitis, MRI had a
220 DIAGNOSIS
sensitivity of 96%, a specicity of 92%, and an overall accuracy of 94%.
185
Scintigraphy with 67Ga and
99m
Tc bone scintigraphy had a sensitivity of 90%, specicity of 100%, and accuracy of 94% when combined. In this study, MRI was as accurate and sensitive as radionuclide scanning for the detection of
Dagirmanjian and colleagues
188
investigated the sensitivity of MRI ndings for vertebral osteomyelitis. ey considered the “classic” MRI changes of vertebral osteomyelitis to include decreased signal of disc and adjacent vertebral bodies on T1-weighted images, increased nonanatomic signal of the disc on T2-weighted images, increased signal of the adjacent ver­tebral bodies on T2-weighted images, and enhancement of the disc and adjacent vertebral bodies. ese investigators found 95% of disc space infection levels had typical T1-weighted vertebral body changes, and 90% had increased nonanatomic signal of the disc on T2-weighted images. Only 54% of the abnormal levels showed increased signal of the vertebral bodies on T2-weighted images, however. Although 84% of patients showed the typical T1-weighted vertebral body and T1- and T2-weighted disc changes, only 49% of cases showed the typical T1- and T2-weighted vertebral body and disc nd­ings as originally described. T1-weighted vertebral body, disc, and endplate changes and T2-weighted disc changes are the most reliable ndings of disc space infection and vertebral osteomyelitis. In the initial stages of vertebral osteomyelitis, when the disc space is not yet involved, it may be dicult to exclude neoplastic disease or compression fracture from the dierential diagnosis using only MRI. Follow-up studies are usually necessary to dene the nature of the lesion further.
Boden and colleagues
189
suggested that in the postopera­tive spine the triad of intervertebral disc space enhancement, anular enhancement, and vertebral body enhancement leads to the diagnosis of disc space infection, with the appropriate laboratory ndings, such as an elevated sedimentation rate. A group of normal postoperative patients, however, has anulus enhancement (at the surgical site), intervertebral disc enhance­ment, and vertebral endplate enhancement without evidence of disc space infection. In these cases, the intervertebral disc enhancement is typically seen as thin bands paralleling the adjacent endplates, and the vertebral body enhancement is associated with type 1 degenerative endplate changes. is pattern should be distinguished from the amorphous enhancement seen within the intervertebral disc with disc space infection.
Staphylococcus aureus is the organism most commonly associated with vertebral osteomyelitis and epidural abscess, accounting for approximately 60% of the cases (Fig. 13.26). S. aureus is ubiquitous, tends to form abscesses, and can infect compromised and normal hosts. Other gram-positive cocci account for approximately 13% of cases, and gram-negative organisms account for approximately 15%. Clinical acute symptoms classically include back pain, fever, obtundation in severe cases, and neurologic decits. Chronic cases may have less pain and no elevated temperature. Rankin and Flothow
190
described the classic clinical course of epidural abscess in four stages: spinal ache, root pain, weakness, and paralysis. Acute deterioration from spinal epidural abscess remains
unpredictable, however. Patients may present with abrupt paraplegia and anesthesia. e cause for this precipitous
course is unknown, but it is thought to be related to a vascular mechanism (e.g., epidural thrombosis and thrombophlebitis, venous infarction).
191,192
e primary diagnostic modality in the evaluation of epi­dural abscess is MRI. MRI is as sensitive as CT myelography for diagnosing epidural infection, but it also allows the exclu­sion of other entities, such as herniation, syrinx, tumor, and cord infarction.
193,194
MRI of epidural abscess shows a so
tissue mass in the epidural space with tapered edges and an associated mass eect on the thecal sac and cord. e epidural
masses are usually isointense to the cord on T1-weighted images and of increased signal on T2-weighted images. Post and colleagues
195,196
recommended that in ambiguous cases either CT myelography or contrast medium–enhanced MRI is necessary for full elucidation of the abscess (Fig. 13.27).
e patterns of MRI contrast medium enhancement of epidural abscess include (1) diuse and homogeneous, (2) heterogeneous, and (3) thin peripheral. Post and colleagues found that enhancement was a very useful adjunct for identi­fying the extent of a lesion when the plain MR image was equivocal, for showing activity of an infection, and for direct­ing needle biopsy and follow-up treatment. Successful therapy should cause a progressive decrease in enhancement of the paraspinal so tissues, disc, and vertebral bodies.
197
Intramedullary Lesions
Diagnostic considerations of pathology involving the intramedul­lary space include neoplasm, vascular malformation, syrinx, granulomatous disease, inammation, or demyelination. Radiographs without intrathecal contrast have no value for nonexpansile cord pathology, with late ndings of cord neoplasm only inferred by canal expansion or osseous destruction. MR imaging can directly visualize the cord and can characterize nonexpansile cord abnormalities.
e imaging ndings of spinal cord neoplasm most com­monly include cord expansion, syrinx formation, and enhancement. For low-grade nonenhancing neoplasms there is typically cord expansion. pansile T2 or STIR hyperintense spinal cord, distribution of signal abnormalities, enhancement, blood degradation byproducts, and its behavior over time (if available) are all useful factors to consider when arriving at an appropriate dierential diagnosis. Transverse myelitis tends to involve longer segments of the cord as opposed to multiple sclerosis, which tends to be patchy and involves the dorsal or lateral aspects of the cord. Enhancement should typically resolve by 2 months when present with multiple sclerosis (Fig. 13.28). Spinal cord infarct can involve the ventral gray matter centrally within the spinal cord; subacute combined degeneration has a more posterior distribution.
Neoplasms
e most common intramedullary neoplasms are gliomas, principally astrocytomas and ependymomas. Ependymomas
201,202
When faced with a nonex-
200
196
198-200
Chapter 13 Spine Imaging 221
SECTION
II
AB
FIG. 13.26 Disc space infection with epidural abscess. (A) Sagittal
T1-weighted magnetic resonance image shows slight decreased signal of L4 and L5 marrow adjacent to disc space and poor denition of distal thecal sac. (B) Sagittal T2-weighted image shows abnormal increased signal from L4–L5 disc space (large arrow) and linear low signal dorsal to L4 and L5 bodies outlining anterior epidural abscess (small arrows). (C) Sagittal T1-weighted image after contrast administration better denes margins of epidural abscess (arrows) by enhancing margin extending inferiorly toward S1 level. Slight abnormal enhancement is present within the disc itself. (D) Axial
D
are cited as the most frequent intramedullary tumors in adults (Fig. 13.29). Although ependymomas may involve any portion of the cord, they most commonly involve the conus medullaris and lum terminale and are the most common primary tumor of the lower spinal cord. Patients with these tumors present in the fourth to h decades of life, oen with back pain.
203,204
A typical appearance is an intradural extramedullary mass involving the lum terminale and cauda equina, although it can appear as fusiform enlargement of the cord itself.
205
Cervi­cal intramedullary tumors may be seen in patients with neurobromatosis type 2 (Fig. 13.30). ese tumors typically enhance and may have intratumoral cysts. e myxopapillary subtype is particularly common in the lumbosacral region, typically appearing as a large, intensely enhancing mass span­ning several vertebral levels. In most cases, the tumors appear as intradural extramedullary lesions because of their bulky exophytic growth, which lls the spinal canal. Overall signal intensities are nonspecic, but because of their highly vascular
T2-weighted image shows loculated abscess as foci of high signal, displacing caudal thecal sac dorsally (arrow).
nature, ependymomas oen show areas of T2-weighted short­ening secondary to the presence of hemosiderin and ferritin, which is strongly suggestive of the diagnosis.
manifest as subarachnoid hemorrhage.
Intramedullary astrocytomas constitute 6% to 8% of primary spine tumors, with a peak incidence in the third to fourth decades of life. Astrocytomas produce focal enlargement and occasionally exophytic growth involving the cord. Of these tumors, 75% to 92% are relatively benign, such as grades 1 and
2. Imaging shows fusiform enlargement of the cord over several segments, whereas T2-weighted MRI shows increased signal intensity reecting tumor and edematous cord. Cysts
are oen associated with these intramedullary tumors. ese cysts may be benign, syringomyelic type of cavities, or actual cysts associated with the tumor.
Hemangioblastomas are unusual cord tumors and typically manifest in the third to fourth decades of life. ey are frequently multiple and seen in association with von
C
206
207
ey also may
222 DIAGNOSIS
A
C
B
FIG. 13.27 Tuberculosis. (A) Sagittal T1-weighted magnetic
resonance image shows large mass involving L5–S2 bodies with epidural extension. L5–S1 disc space is normal. (B) T2-weighted image shows mass as heterogeneous high signal. (C) After contrast administration, T1-weighted image better denes epidural abscess with peripheral enhancement (arrows).
Hippel–Lindau disease.
208-213
ese lesions most oen mani­fest as dorsal intramedullary masses containing a nodule that enhances, although these vary by the amount of cyst compo­nent and solid component. ere may be extensive widening of the cord, showing increased signal intensity on T2-weighted images related to cord edema and extending several segments away from the nidus itself.
Occasionally, metastatic disease may manifest as an intramedullary enhancing mass. Carcinoma of the lung and breast is the most common, with melanoma, lymphoma, and renal cell carcinoma also reported.
214,215
Spread of intra­cranial neoplasms such as ependymoma and glioma may also seed the leptomeninges and produce direct involvement of the cord.
216-218
Benign intramedullary tumors are uncommon, but cavern- ous angiomas (cavernous malformations) can occur in the cord with typical signal characteristics of speckled increased
and decreased signal on T1-weighted images and evidence of hemosiderin deposition on T2-weighted images (Fig. 13.31).
Inammation
e various causes of inammatory myelopathies include multiple sclerosis, postviral demyelinating disease, viral infection, pyogenic infection, and granulomatous disease. e archetypal inammatory lesion is multiple sclerosis (Fig.
13.32). e spinal cord is the site of much clinical involvement
in patients with multiple sclerosis; however, imaging of the spinal cord has always been subordinate to brain imaging in radiologic investigations of multiple sclerosis. Because some of the clinical disease activity in multiple sclerosis is related to the spinal cord, it is important to correlate cord disease with clinical activity to gain further insights into the nature of disability in these patients and to correlate objective