Notes
Slide Show
Outline
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Joint diseases
  • OSCE Review
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Approach to differential diagnosis
  • Sutton’s law: “that is where the money is”
    • DJD/DDD, RA, CPPD and DISH
  • Law of parsimony
    • One diagnosis cannot always explain everything
  • Demographic information
    • Prevalence in age, gender, etc.
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Approach to differential diagnosis
  • Radiographic hallmarks
    • Osteophytes, erosions
  • Real estate: location, location, location
    • Pattern approach
    • Know where to look
    • Know what affects where
  • ABCDS of joint diseases
    • Alignment
    • Bone
    • Cartilage
    • Distribution
    • Soft Tissue

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DJD
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Degenerative Joint Disease
  • Primary Osteoarthritis
    • No evidence of underlying etiology


  • Secondary Osteoarthritis
    • Abnormal forces including obesity, trauma, and joint deformity.
    • Pre-existing cartilage pathology such as rheumatoid arthritis, fractures and meniscal damage.
    • Collapse of subchondral bone, such as avascular necrosis and osteoporosis.


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DJD-risk factors
  • systemic & local risk factors
    • age- ­DJD w/ ­age
    • gender- females ­ DJD of hands, knees
    • obesity- ­DJD of knees & hips
    • trauma- most significant local factor
    • physical activity- ­DJD w/ high impact

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General Radiology Features
  • asymmetric loss of joint space
  • osteophytes
  • enthesopathy
  • subchondral sclerosis
  • subchondral cysts
  • intrarticular loose bodies
  • ankylosis (rare)
  • subluxation
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Joint misalignment
  • degeneration leads to joint laxity
  • muscle tension and gravity may cause misalignment
  • redistribution of forces leads to bone deformity


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Degenerative joint disease
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Degeneration- hands
  • common, especially among middle-aged postmenopausal women
  • enlarged soft tissue nodes of DIPs (Heberden’s nodes) and PIPs (Bouchard’s nodes)



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Radiology of the Hands
  • Target Locations....
    • distal interphalangeal joints
    • proximal interphalangeal joints
    • 1st metacarpal-carpal joints
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Synoviochondrometaplasia
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Synovial Osteochondrometaplasia
  • multiple intra-articular loose bodies
  • synovial tissue metaplasia that produces cartilaginous masses
  • may ultimately ossify to become visible radiographically
  • common in the knee and are also seen about the hip, ankle, shoulder and wrist.
  • "joint mice", with joint locking.
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RSDS
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Reflex sympathetic dystrophy syndrome
  • Clinical
    • pain
    • vasomotor disturbances
    • trophic skin changes
      • skin atrophy
      • pigmentation abnormalities
    • Synonyms
      • causalgia, Sudeck's atrophy or osteodystrophy, shoulder-hand syndrome
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Etiology theory
  • lesion or injury
  • painful impulses travel to the spinal cord, "internuncial pool"  reflexes
  • provoked efferent pathways to the peripheral nerves
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Imaging
  • too nonspecific to make the diagnosis in the absence of clinical information
  • soft tissue swelling
  • regional osteoporosis
    • aggressive and severe
    • significant juxtaarticular osteoporosis
    • generally a unilateral process
    • entire extremity
    • osteoporosis may be patchy
    • joints are usually maintained
    • radionuclide imaging
      • shows increased uptake of tracer in the articular regions
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Gout
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Gout
  • A sodium urate induced arthropathy (a metobolic joint dz)
  • disorder of purine metabolism
  • principally males
  • chronic hyperuricemia
  • renal disease
  • red, swollen and extremely painful joints
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Radiology of Gout
  • tophi - soft tissue nodules adjacent to the joint
  • tophi may contain amorphous calcification
  • para-articular erosion with sclerosis and "overhanging edge" sign
  • often only seen after chronic years of disease
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Gout
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HADD
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Hydroxyapatite Deposition Disease (HADD)
  • Commonly seen about the:
    • shoulder, elbow, wrist, hip, knee, ankle, spine
  • Other names include:
    • calcifying tendinitis and bursitis
    • peritendinitis calcarea
  • MC in the supraspinatus tendon
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Case 7
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Rheumatoid arthritis (RA)
  • MC inflammatory arthritis (1-2%)
  • marked by inflammatory, hyperplastic synovitis (pannus)
  • F>M, 1:2-7; usually 20-50 yoa
  • >60 years, F=M
  • elevated ESR
  • 70 to 80% +RA factor (5% in general pop)
  • +ESR, +ANA


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RA-radiographic progression
  • Periarticular soft tissue swelling
  • juxtaarticular osteoporosis, later generalized
  • narrowed joint spaces, symmetrical loss
  • erosions, beginning in bare areas
  • subchondral geodes
  • joint deformity due to conn. tissue laxity
  • secondary OA, possible ankylosis
  • pattern of involvement in hands: PIP, MCP jts
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RA Cervical Spine
  • more common than other axial sites
  • 50% of patients within 10 yrs
  • atlantoaxial subluxations
  • dens erosion
  • apophyseal joint disease


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Odontoid erosions
  • Synovial joints:
    • 1. Between dens and anterior arch
    • 2. Between the dens and transverse ligament
    • 3. At the tip of dens
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Lupus
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Systemic Lupus Erythematosis
  • rheumatoid type (seropositive)
  • female, 9F:1M; MC among those 20-40 yoa
  • ESR elevated, ANA positive
  • Marked subluxation
    although the joints integrity
    is relatively normal
  • butterfly rash
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SLE-distribution
  • hands-
    • MCP and PIP usually affected
    • ligament laxity results in reversible nonerosive ulnar deviation of digits (classic & <50% of patients)
    • swan-neck & boutenniere deformity
  • spine- ­ADI (8.5%)
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     Scleroderma
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Scleroderma
Progressive Systemic Sclerosis
  • Of unknown etiology.  Causes small vessel disease and fibrosis in multiple organ systems.  Scleroderma is the cutaneous manifestation of the disease.
  • 3F:1M ratio
  • 20 to 50 years
  • hands- soft tissue atrophy, osseous resorption (acro-osteolysis), & subcutaneous calcification
  • RF positive


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Diffuse Idiopathic Skeletal Hyperostosis
  • very common, MC males over 50
  • incidence among diabetics: 13-49%, in general population (8-20%)
  • neck stiffness, dysphagia in 20%
  • exuberant proliferation of bone at osseous sites of ligament and tendon attachments (enthesopathy)
  • spinal and extraspinal sites
  • most marked along the anterior longitudinal ligament (ALL) of the middle & lower thoracic, upper lumbar, and lower cervical regions



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Radiology of DISH
  • Multiple levels of flowing ossification  involving the anterior vertebral body margins with ankylosis ...... an enthesopathy.
  • Preservation of disc height (minimal evidence of disc disease)
  • Absence of sacroiliitis (excludes ankylosing spondylitis)
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          OPLL
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Ossification of the Posterior Longitudinal Ligament
  • Sometimes found in conjunction with DISH, but is also seen as an distinct entity.
  • present in 40-50% of DISH patients
  • X-ray- linear radiodense strip along posterior vertebral body margins, usually in cervical spine
  • can result in loss of the sagittal diameter of the spinal canal, with resultant myelopathy.
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Atrophic neuropathic arthropathy
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Neuropathic arthropathy (Charcot joints)
  • joint abnormalities secondary to impaired pain perception or proprioception
  • distribution is usually monoarticular and depends on underlying abnormality
  • two categories based on imaging
    • Hypertrophic- bone forming
    • Atrophic- resorptive




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Neurotrophic- clinical
  • Suspected in patients with a painful swollen joint, neurological disorder, and radiographic evidence of bone destruction
    • weightbearing joints- hypertrophic
    • non-weightbearing joints- atrophic
  • decreased pain sensation and proprioception
  • 30% will have pain making diagnosis difficult
  • swollen unstable joint
  • DDx from infection, advanced DJD, or CPPD


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Etiologies
  • congenital indifference to pain
  • alcoholism
  • diabetes
  • syphilis
  • syringomyelia
  • trauma
  • steroids
  • leprosy
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Case 14
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Osteitis condensans illi
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Osteitis Condensans ilii
  • MC in women than men
  • etiology unknown:
    • theories: stress across the SI joint
    • hypervascularity of pregnancy
  • triangular radiodensities on illium side of SI joint, usually bilateral.
  • the SI joint itself is usually normal
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Early AS
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Ankylosing spondylitis (AS)
  • MC seronegative spondyloarthropathy
  • affect 0.1-0.2%
  • 1:1 to 1:10 female to male ratio
  • 90% positive HLA-B27 (6-8% in general population)
  • Axial: SI and spine
  • Appendicular: proximal large joints of extremities (rhizomelic)
  • Enthesis (attachment of ligaments and tendons to bone)


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Enthesis
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Sacroiliac involvement
  • Classic initial site of skeletal involvement
    • hazy loss of subchondral (cortical) definition
    • erosions and joint space widening
    • fusion
  • 50% will progress to fusion
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Management
  • management is aimed at a long-term plan to prevent, decrease, or delay joint and postural deformities
  • NSAIDS to limit joint inflammation and pain
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AVN
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AVN
  • Osteonecrosis can be idiopathic or secondary to a number of conditions that reduce blood supply to the bone such as an intraluminal abnormality, an extrinsic compression, or a combination of both.
  •  CT scans, MRIs, and bone scans play a significant role in diagnosing the disease at an early stage to reduce the number and/or severity of complications and morbidity associated with the disease.
  • MC cause adults: corticosteroids
  • MC cause in kids: idiopathic
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Plain film-AVN
  • no radiographic evidence early in the disease, first finding is osteopenia, followed by fissures, sclerosis, and fragmentation
  • subchondral fractures
  • heals with articular deformity leading to DJD
  • MRI and bone scan are more sensitive



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Why is this not just DJD?
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Calcium Pyrophosphate Deposition Disease
  • Arthropathy characterized by intra-articular deposition of calcium pyrophosphate crystals.
    Synonyms:
  • CPPD
  • pseudogout
  • chondrocalcinosis


  • symptoms before age 50 are uncommon
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Radiology of CPPD
  • radiographic evidence of chondrocalcinosis of hyaline or fibrocartilage (linear radiodensities)
  • common sites include the knee (menisci), wrist, MCPs, and symphysis pubis
  • less common in capsule, tendons, and ligaments
  • intraarticular deposits of CPPD may degrade cartilage cause severe joint degeneration
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DJD
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Uncinate hypertrophy (DJD)
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Bouttonnière / Swan neck
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Osteomyelitis
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Carpal coalition
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Sacroilitis
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Gout
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Pelligrini-Stieda (HADD)
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Bilateral DJD (hip)
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Synoviochondrometaplasia
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DJD primary and secondary
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Osteitis condensans ilii
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CPPD and DJD
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Synoviochodrometaplasia
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Neuropathic arthropathy
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Healed AVN
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Hemivertebra
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OCI
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DJD and patella removal
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AS ?