MRI in deformity

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Status
Done

Adults

Indication

  • When lower extremity pain is present
    • For adult spinal deformity
      • Neurological symptoms reported in 59–85% of patients with ASD
      • Severe symptoms (VAS > 5) present in > 40% of patients
        • Most common are isolated radiculopathy followed by claudication, neurological deficit, and myelopathy

Can identify

Disc degeneration
  • Pfirrmann grading
      • A complete evaluation of disc status (especially at LSJ) is critical to define whether to extend the fusion to the Sacrum/pelvis
       
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Modic endplate changes;
  • Oh I See; Oedema I both bright, See Shadow)
  • Modic type I:
    • Pathology
      • bone marrow oedema and inflammation
    • T1: low signal
    • T2: high signal
    • T1 C+ (Gd): enhancement
    • Clinical significance
      • associated with low back pain
      • ? infection being a potential aetiological factor for lower back pain.
        • Albert et al. 2013: double blind RCT
          • co- amoxiclav for 100 days
          • back pain + Modic type 1 changes
          • Findings were encouraging and demonstrated a statistically significant improvement in disability indices in the antibiotic group versus the placebo group.
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          • This has been disproven by other external studies (Need to find these studies)
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  • Modic type II:
    • Pathology
      • Marrow ischaemia → Normal red haemopoietic bone marrow conversion into yellow fatty marrow
    • T1: high signal
    • T2: iso to high signal
    • Clinical significance
      • associated with low back pain
  • Modic type III:
    • Pathology
      • Subchondral bony sclerosis
    • T1: low signal
    • T2: low signal
Central canal stenosis
  • Canal stenosis occurs in ~8% of patients with ASD
  • Most common symptom is neurological claudication
  • Schizas grading
      • Grade A: No or minor stenosis
        • A1: the rootlets lie dorsally and occupy less than half of the dural sac area.
        • A2: the rootlets lie dorsally, in contact with the dura but in a horseshoe configuration.
        • A3: the rootlets lie dorsally and occupy more than half of the dural sac area.
        • A4: the rootlets lie centrally and occupy the majority of the dural sac area.
      • Grade B stenosis: Moderate stenosis
        • the rootlets occupy the whole of the dural sac, but they can still be individualized. Some CSF is still present giving a grainy appearance to the sac.
      • Grade C stenosis: Severe stenosis
        • no rootlets can be recognized, the dural sac demonstrating a homogeneous gray signal with no CSF signal visible. There is epidural fat present posteriorly.
      • Grade D stenosis: Extreme stenosis
        • in addition to no rootlets being recognizable there is no epidural fat posteriorly.
       
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Synovial cyst
  • Originates from the joint
  • Capsulated, iso/hyperintense in T2
  • Can be aspirated
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Paraspinal muscle health (Goutallier classification)
  • Evaluation of fatty infiltration in paraspinal muscles
  • Jun 2016
    • Fatty degeneration (FD) of paraspinal muscles was significantly correlated with:
      • Higher age (r = 0.393)
      • Increased pelvic tilt (r = 0.430)
      • Increased sagittal vertical axis (SVA) (r = 0.488)
      • Greater PI–LL mismatch (r = 0.479)
      • More kyphotic thoracic alignment (r = −0.559; negative correlation)
      • Less lumbar lordosis (LL) (r = −0.505)
    • Muscle mass (LM) was positively correlated with LL (r = 0.342), and negatively with PI–LL mismatch (r = −0.283).
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  • Facet hypertrophy
  • Pedicle enlargement
  • Foraminal encroachment

Paediatric (EOIS, LOIS)

  • MRI spine including craniocervical junction to sacrum is required
  • Indication
      • Rapid progression
      • Excessive kyphosis
      • Structural abnormalities
      • Neurologic symptoms or pain
      • Atypical curve pattern (left thoracic curve, short angular curve, apical kyphosis)
      • Foot deformities
      • Asymmetric abdominal reflexes
        • A syrinx is associated with abnormal abdominal reflexes and a curve without significant rotation
  • Identify CNS causes (e.g. syrinx, Chiari malformation, tethered cord).