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Title: Brant


1
Brant Helms Conference
  • Chapters 10 11

Andrew Knoll, MD UCI Radiology October 22, 2008
2
Preliminary Quiz
3
Case 1
4
Case 2
5
Case 3
6
Case 4
7
Case 5
8
Case 6
9
Clinical Syndromes
  • Myelopathy Emergency MRI
  • Cord compromise (compression, intrinsic lesion,
    inflammatory process)
  • Bowel/bladder incontinence, spasticity, weakness,
    ataxia
  • May develop sensory/motor level, but lesion may
    be several levels higher than expected
  • Radiculopathy Not an emergency
  • Impingement of spinal nerve, usually sec to
    degenerative changes
  • Sensory/motor level correlates well with lesion

10
Imaging modalities / techniques
  • MR study of choice for evaluating myelopathy and
    radiculopathy
  • CT myelography if MR contraindicated (plain film
    myelography rarely done)
  • CT better than MR for spondylolysis (MR not very
    good), and for detection of calcification
    (tumors, OPLL, spurs, bone fragments following
    trauma)

11
Differential Diagnosis by Location
  • Intramedullary (within cord itself) cord
    appears widened and CSF space appears thinned in
    all views
  • DDX Damn Cord is Trouble
  • Demyelin. Dz (MS, ADEM, transverse myelitis)
  • Cysts (syringohydromyelia, neuroepithelial cyst)
  • Infarct ( also AVM/AVF)
  • Tumor (AHEM mnemonic)
  • Intradural Extramedullary widened csf/contrast
    column adjacent to the mass, csf/contrast forms
    acute angles with the mass
  • DDX Meningioma, schwannoma, neurofibroma (Big
    3), also dermoid, epidermoid, lipoma, arachnoid
    cyst, drop met, AVM

12
Differential Diagnosis by Location
  • Extradural or epidural (outside the dural sac,
    within spinal canal) csf forms obtuse angle
    with mass, mass effaces epidural fat and thins
    csf space adj. to the mass
  • DDX think degenerative and nondegenerative
  • Degen herniated disc, synovial cyst, osteophyte
  • Nondegen epidural hematoma, epidural abscess,
    lymphoma/chloroma, mets, myeloma, EM
    hematopoiesis

13
Inflammatory cord lesions
  • Myelitis inflam process directly involving
    cord, results in myelopathy
  • Transverse myelitis nonspecific myelitis
    confined to specific level(s) not a disease but
    rather a category of diseases
  • On imaging, it is not transverse variable
    size, but usually extends 3 or 4 spinal levels

14
Inflammatory cord lesions
  • MS / Devics
  • High T2, usually w/o signif. change in cord
    caliber
  • In acute phase, may see cord expansion,
    enhancement (tumefactive), or restricted
    diffusion
  • Remember to look upstairs
  • SLE
  • Necrotizing arteritis ? cord ischemia
  • Diffuse areas of high T2 edema, usually w/o
    enhancement less well-defined than MS plaques
  • Dramatic improvement with steroids
  • Rhematoid Arthritis
  • Pannus (extradural mass) destroys transverse
    ligament of C1, dens slides posteriorly resulting
    in cord compression (extradural process)
    symptoms worsen on flexion
  • DDX fibrous pseudotumor seen with os odontoideum
    and other unstable spinal anatomy

15
Inflammatory cord lesions
  • Radiation myelitis
  • Peaks 6-12 mos post XRT
  • High T2 /- enhancement
  • Clue is marrow change (fatty replacement)
  • Postviral myelitis (ADEM)
  • Clinical high fever, followed in 4 weeks by
    rapid onset motor, sensory, and autonomic
    deficits referable to specific level(s)
    (transverse myelitis)
  • Also can occur following vaccinations
  • Focal areas of edema and cord expansion
  • In contradistinction to Guillain-Barre, which is
    ascending paralysis due to peripheral nerve
    involvement (also postviral)
  • Arachnoiditis (postsurgical, infectious, etc.)
  • Clumping of cauda equina nerve roots, empty sac
  • Neurosarcoid multiple nodular enhancing areas
  • Pantopaque arachnoiditis
  • Recognize high signal on T1 (lipid-based contrast)

16
Postviral myelitis
  • DDx
  • MS / Devics
  • SLE
  • Sarcoid
  • Infarct
  • Neoplasm

17
Guillain-Barre Syndrome
  • DDx
  • Infection (e.g., CMV)
  • Meningeal carcinomatosis
  • Granulomatous disease

18
Postoperative lumbar arachnoiditis
19
Infection
  • Osteomyelitis/discitis
  • Hematogenous infection ? endplate ? disc ?
    vertebral body (osteomyelitis/discitis complex) ?
    seed epidural space ? extend to paraspinal ST
    (e.g., psoas)
  • In children, disc has rich blood supply and may
    be primarily infected
  • Epidural abscess
  • Often extend several vertebral levels
  • Frequently cause cord compression
  • Subdural empyema (rare) usually assoc. with
    violation of the dura (surgery), may progress to
    meningitis
  • Cord Abscess (rare) appears similar to brain
    abscess

20
Infection
  • Pyogenic
  • Staph most common, followed by Gram negs.
  • Salmonella assoc c sickle cell dz
  • Severe back pain unrelieved by positioning (vs.
    DJD)
  • On plain film, typical to see disc destruction ?
    disc space narrowing and irregularity (vs.
    sparing of disc with TB)
  • MRI abnormal signal and enhancement in disc and
    bone, /- paraspinous ST mass

21
Pyogenic osteomyelitis/discitis
22
Non-Pyogenic Infections
  • More indolent course
  • Diagnostic challenge b/c immunosuppressed pts.
    are at risk for both infxn and neoplasm
    (mets/lymphoma) often requires biopsy
  • TB (Potts)
  • Slow collapse of usually more than one vert
    bodies, spreads subligamentous
  • Leads to gibbus deformity, cord compression
  • Tends to spare disc
  • Psoas abscess common
  • May also cause meningitis
  • Fungal
  • Clasically Candida and Aspergillus in
    immunosupressed pts, also cocci, blastomycosis,
    and cryptococcus
  • Cocci spares disc like TB
  • May be hard to distinguish from neoplasm

23
Tuberculous spondylitis (Potts Dz)
  • Ddx
  • Fungal
  • Mets
  • Myeloma
  • Lymphoma
  • Pyogenic infxn

24
Neoplasms Intramedullary
  • Classic plain film finding focal widening of
    interpedicular distance
  • AHEM (astrocytoma, hemangioblastoma, ependymoma,
    mets)
  • Astrocytoma
  • 75 cervical and upper thoracic rare in
    conus/filum
  • Fusiform cord widening and T2 hyperintensity
    extending several levels
  • Can be exophytic, mimic extramedullary
  • Ependymoma
  • Most common cord tumor
  • Usually benign
  • 60 in conus / filum
  • Filum is usually myxopapillary type
  • Hemorrhage and cystic changes common
  • Hemangioblastoma
  • Densly enhancing nidus /- cyst (very classic)
  • Assoc c Von Hipple Lindau
  • 40 extramedullary
  • 20 multiple

25
Ependymoma
Differentation of Ependymoma and Astrocytoma is
Very Difficult !!!
26
Astrocytoma
27
Hemangioblastoma associated syrinx
28
Neoplasms Intradural/Extramedullary
  • Meningioma
  • Most commonly in the thoracic region
  • 80 in women
  • May have extradural component
  • May have dural tail and/or calcifications
  • Homogeneous enhancement (just like cranial ones)
  • Nerve Sheath Tumors (Schwannoma/Neurofibroma)
  • Histologic difference in that neurofibroma
    diffusely infiltrates nerve w/o encapsulated
    margin while schwannoma remains outside n. (same
    on imaging)
  • Either can have classic dumbbell shape with
    extension through neural foramen

29
Thoracic meningioma
Note flaring of csf space adj to mass
30
Cystic Schwannoma
31
Neurofibromatosis Type 1
32
Neoplasms Intradural/Extramedullary
  • Intrathecal drop mets
  • From primary CNS tumors (medullo, ependymoma,
    germinoma, choroid plexus carcinoma)
  • Leptomeningeal metastases (breast, lung,
    leukemia)
  • Inflammatory rxn carcinomatous meningitis
  • Multiple intradural nodules
  • DDX infectious meningitis, blood

33
Leptomeningeal Metastases
34
Extradural Masses
  • Most commonly degenerative (disc, etc.), followed
    by neoplasm (mets most common breast, lung
    prostate)
  • Mets typically low T1 high T2 within vertebrae
    (vs. the ubiquitous hemangioma high T1) and
    usually enhance
  • Exception Sclerotic mets (prostate) may be low
    on all sequences
  • Compression fracture
  • Ddx osteoporosis, mets, infection
  • Signs of mets noncontiguous vertebral levels,
    spares discs, , marked involvement of pedicles

35
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36
Benign compression fracture
37
Pathologic fracture (lung met)
38
Other Extradural masses
  • Direct extension of paraspinous tumor
  • Retroperitoneal/mediastinal tumors
  • Neuroblastoma, ganglioneuroma, lymphoma, Pancoast
    lung tumors
  • Frequently infiltrate canal through neural
    foramina
  • Leukemia
  • Diffuse, even replacement of marrow by cellular
    tumor
  • Chloroma solid leukemic infiltrate may involve
    epidural space and cause cord compression
  • Lymphoma
  • 2 presentations metastatic vertebral body
    involvement or invasion through neural foramina
  • Often extensive epidural/paraspinous mass
    associated with it, can mimic infxn such as TB
  • Multiple myeloma
  • Multiple low T1 foci or diffuse low T1 signal in
    spine (On T1, vertebrae should always be
    brighter than disc)
  • Myelofibrosis
  • Very dark marrow on T1 and T2 (ddx prostate
    mets)
  • Primary Bone Tumor

39
Vascular
  • Cord infarct (rare)
  • Usually s/p thoracic surgery (aortic aneurysm
    repair), but can also be thromboembolic
  • Appears bright on T2 ? enhancement ? later
    myelomalacia
  • Vascular malformations
  • Intramedullary AVM congenital nidus of abnormal
    vessels
  • Cord hemorrhage ischemia sec to steal
    phenomenon
  • Extramedullary usually AVF (SDAVF)
  • Venous HTN ? cord congestion / edema
  • High T2, expansion, and enhancement in conus, /-
    dilated veins
  • Pitfall CSF pulsation artifact (particularly in
    thoracic spine) may be confused with dilated
    spinal veins limitation of MR

40
Cord infarct
41
Spinal AVM
  • MR
  • Flow voids
  • Edema
  • Punctate enhancement
  • Angio
  • Enlarged anterior spinal artery (of Adamkiewicz)
  • Nidus
  • Venous shunting

42
Syringohydromyelia (syrinx)
  • Hydromyelia dilated central canal, lined by
    ependyma
  • Syringomyelia cavity outside central canal,
    lined by glia
  • Difficult to distinguish, hence
    syringohydromyelia
  • Etiologies Chiari (usually I), trauma, tumor,
    inflammation, ischemia

43
Syrinx secondary to Chiari I
44
Congenital lesions
  • Pediatric intraspinal masses are most commonly
    congenital
  • Tethered cord
  • Conus normally at L2 in newborns, T12/L1 adults
  • Below that level tethered, but hard to tell
    exact level b/c tethered roots form a taut mass
    therefore must follow serially
  • May present in adulthood with gait abnormalities
  • Assoc with spinal dysraphism, lipoma
  • Fatty filum
  • Not associated with tethering
  • Asymptomatic
  • May have to follow

45
Congenital lesions
  • Caudal regression syndrome
  • Distal L spine sacrum hypoplastic or absent
  • Blunted appearance of conus
  • Associated with cardiac renal anomalies
    (mesoderm problem)
  • Assoc c maternal diabetes
  • Cystic lesions
  • Perineural (Tarlov) cystincidental usually
    sacral represent dilated nerve root sleeves
  • Anterior sacral meningocele
  • Arachnoid cyst isointense to CSF
  • Ddx epidermoid
  • Complication of LP (acquired arachnoid cyst)
  • Neurenteric cyst (notochord communicates with
    foregut)
  • Look for canal of Kovalevsky

46
Congenital lesions
  • Congenital scoliosis
  • If severe or early or associated with vertebral
    anomalies on plain film, MR is indicated to rule
    out intraspinal pathology
  • Diastematomyelia
  • Sagittal cleft (split cord)
  • Midline bony / fibrocartilagenous spur (plain
    films, CT)
  • Diplomyelia- extremely rare

47
Caudal regression syndrome
48
Extradural Arachnoid Cyst
Note effacement of epidural fat and narrowing of
CSF space adjacent to the mass
49
Diastematomyelia (and tethered cord)
50
Trauma
  • Cord contusion
  • Usually (not always) occur at site of fx sec to
    bony impingement
  • Edema is bad blood is really bad (irreversible)
  • Later, myelomalacia potentially can enlarge c
    csf entry, evolve into syrinx
  • EDH
  • Much more common than SDH (opposite of brain)
  • Venous bleeding
  • Nerve root avulsion
  • Most common in c-spine
  • Classic cause birth trauma (shoulder dystocia)
  • CSF leaks into epidural space through rent in
    dura and arachnoid from missing nerve
    (pseudomeningocele)
  • see dilated lat recess w/o nerve roots

51
Epidural Hematoma
52
Chapter 11
  • Lumbar Spine Disc Disease and Stenosis

53
Degenerative disc disease
  • Terminology bulge, broad-based protrusion,
    protrusion, extrusion, sequestration (free
    fragment)
  • Surgeons dont care what you call it. Only
    concerned with whether the abnormality is
    responsible for pts symptoms
  • Most important to describe effect on canal and
    foramina
  • Extrusion disc material above or below disc
    space
  • Free fragments
  • Signal often different from parent disc
  • Lateral disc (beyond neural foramen) mimic sx of
    central protrusion one level cephalad because
    they affect the root that has already exited
    spinal canal
  • Ex central disc protrusion at L3/4 impinges on
    L4 nerve root, but far lateral disc at L4/5 also
    can impinge on L4 nerve root

54
Disc extrusion with free fragment
55
Far lateral disc herniation
56
Spinal Stenosis
  • Central spinal canal stenosis
  • Measurements of spinal canal not considered
    valuable
  • Instead, mention if thecal sac is round or
    compressed and give subjective assessment of
    severity
  • Most common causes are hyertrophic facet djd and
    buckling/hypertophy of ligamentum flavum, /-
    superimposed disc protrusion/bulge
  • Less common causes Pagets, achondroplasia,
    post-traumatic, severe spondylolisthesis
  • Often exacerbated by background of congenitally
    short pedicles
  • Lateral recess stenosis ( where the nerve roots
    lie after leaving thecal sac but before entering
    neural foramen
  • Same etiologies as neural foraminal stenosis
  • Neural foraminal stenosis
  • In L spine, nerve root in the sup portion of NF
    and disc inferior portion
  • Most common cause is djd of facets, less commonly
    due to lateral disc protrusion, free fragment or
    postop scarring

57
Spondylolysis / spondylolisthesis
  • Spondylolysis
  • CT superior to MR for detection
  • Best seen on axial slices as laminar defect
    (looks like facet joint but not at disc level)
  • Presumably stress fx
  • Isolated spondylolysis usually asymptomatic
  • Spondylolisthesis
  • Bilateral pars defects
  • Pseudospondylolisthesis due to facet dz (mild,
    most common at L4-5)
  • Divide vert into fourths (grade 1-4)
  • Significant listhesis may cause canal and/or
    neuroforaminal stenosis

58
Spondylolysis / spondylolisthesis
59
Marrow Endplate Changes (Modic)
  • Type 1 low T1, high T2 (edema)
  • Inflam response to DDD
  • Ddx infxn (disc bright on T2 c infxn)
  • Type 2 high T1, high T2 (fat)
  • Most common
  • Type 3 low T1, low T2 (Sclerosis)

60
Quiz
  • Do you have the spine?

61
Case 1
  • Findings
  • Scalloping of posterior vertebral bodies by dural
    ectasia
  • Lateral meningocele

Neurofibromatosis Type 1
62
Case 2
Findings enhancement of ventral nerves
Guillain-Barre Syndrome
63
Case 3
Spinal dural AV Fistula
Findings enhancement and high T2 singal in the
conus and serpentine flow voids which enhance.
MRA shows serpentine high sig. DDx SDAVF, AVM
64
Case 4
Hemangioblastomas in von Hippel-Lindau disease
Findings multiple enhancing intradural (probably
intramedullary) nodules in C, T, and L spine,
with associated lumbar syrinx
65
Case 5
  • Findings
  • Multiple low T1 high T2 enhancing lesions
    throughout
  • Epidural (subligamentous) enhancement
  • Paraspinal peripherally enhancing mass
  • Ddx
  • TB
  • Fungal
  • Mets
  • Myeloma
  • Lymphoma

Tuberculous spondylitis
66
Case 6
  • Findings
  • Intradural / extramedullary CSF-signal lesion
    with peripheral enhancement, compressing conus
  • Ddx
  • Cystic Schwannoma
  • Infected arachnoid cyst
  • Epidermoid
  • Necrotic met
  • Necrotic exophytic cord tumor

Schwannoma
67
Case 7
68
Case 8
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