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Updated: Dec 5 2024

Legg-Calve-Perthes Disease

Images
https://upload.orthobullets.com/topic/4119/images/lcp.jpg
https://upload.orthobullets.com/topic/4119/images/Herring Group A xray_moved.jpg
https://upload.orthobullets.com/topic/4119/images/Herring Group B xray_moved.jpg
https://upload.orthobullets.com/topic/4119/images/bc..jpg
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https://upload.orthobullets.com/topic/4119/images/gage sign.jpg
  • summary
    • Legg-Calve-Perthes Disease is an idiopathic avascular necrosis of the proximal femoral epiphysis in children.
    • Diagnosis can be suspected with hip radiographs. MRI may be required for diagnosis of occult or early disease. 
    • Treatment is typically observation in children less than 8 years of age, and femoral and/or pelvic osteotomy in children greater than 8 years of age.
  • Epidemiology
    • Incidence
      • affects 1 in 10,000 children
    • Demographics
      • 4-8 years is most common age of presentation
      • male to female ratio is 5:1
      • higher incidence in urban areas
      • socioeconomic class
        • higher among lower socioeconomic class
      • latitude
        • higher incidence in high latitude (low incidence around equator)
      • race
        • Caucasian > East Asian and African American
    • Anatomic location
      • bilateral in 12%
        • asymmetrical, asynchronous involvement
          • rarely at the same stage of disease
        • symmetrical involvement suggests MED (multiple epiphyseal dysplasia)
    • Risk factors
      • positive family history
      • low birth weight
      • abnormal birth presentation
      • second hand smoke
      • Asian, Inuit, and Central European descent
  • Etiology
    • Pathophysiology
      • osteonecrosis occurs secondary to disruption of blood supply to femoral head
        • followed by revascularization with subsequent resorption and later collapse
          • creeping substitution provides pathway for remodeling after collapse
      • proposed mechanisms
        • possible association with abnormal clotting factors (Protein S and Protein C deficiencies)
          • controversial etiology
          • thrombophilia has been reported to be present in 50% of patients
          • up to 75% of affected patients have some form of coagulopathy
        • repeated subclinical trauma and mechanical overload lead to bone collapse and repair (multiple-infarction theory)
          • damages result from epiphyseal bone resorption, collapse, and the effect of subsequent repair during the course of disease
        • maternal / passive smoking aggravates
    • Associated conditions
      • associated with ADHD in 33% of cases
      • bone age is delayed in 89% of patients
  • Classification 
    • Lateral Pillar Classification
      • has best agreement and is most predictive
      • determined during fragmentation stage 
        • usually occurs 6 months after the onset of symptoms
        • based on the height of the lateral pillar of the capital femoral epiphysis on AP imaging of the pelvis
        • designed to provide prognostic information
        • limitation is that final classification is not possible at initial presentation due to the fact that the patient needs to have entered into the fragmentation stage radiographically
        • Lateral Pillar (Herring) Classification
        • Group A
        • Lateral pillar maintains full height with no density changes identified
        • Consistently good outcome
        • Group B
        • Maintains >50% height
        • Poor outcome in patients with bone age > 6 years
        • Group B/C
        • Lateral pillar is narrowed (2-3mm) or poorly ossified with approximately 50% height
        • Recently added to increase consistency & prognosis of classification
        • Group C
        • Less than 50% of lateral pillar height is maintained
        • Poor outcomes in all patient
    • Waldenstrom classification
        • Stages of Legg-Calves-Perthes (Waldenström)
        • Initial
        • Infarction produces a smaller, sclerotic epiphysis with medial joint space widening
        • Radiographs may remain occult for 3 to 6 months
        • Fragmentation
        • Begins with presence of subchondral lucent line (crescent sign)
        • Femoral head appears to fragment or dissolve
        • Result of revascularization process with bone resorption producing collapse with subsequent patchy density and lucencies
        • Hip related symptoms are most prevalent
        • Lateral pillar classification based on this stage Can last from 6m to 2y
        • Reossification
        • Ossific nucleus undergoes reossification with new bone appearing as necrotic bone is resorbed
        • May last up to 18m
        • Healing or remodeling
        • Femoral head remodels until skeletal maturity
        • Begins once ossific nucleus is completely reossified; trabecular patterns return
    • Catteral Calssification
      • Emphasizes extent of head involvement and outcome (see groups below)
      • Applied during fragmentation stage when the necrotic segment is demarcated from the viable portion
      • Catterall also described head
      • At-risk signs that are associated with poor outcomes
        • Gage sign (V-shaped radiolucency in the lateral portion of the epiphysis and/or adjacent metaphysis)
        • Calcification lateral to the epiphysis
        • Metaphyseal cyst
        • Lateral subluxation of the femoral head
        • Horizontal proximal femoral physis
        • Catterall Classification
        • Based on degree of head involvement
        • Group I
        • Involvement of the anterior epiphysis only
        • Group II
        • Involvement of the anterior epiphysis with a central sequestrum
        • Group III
        • Only a small part of the epiphysis is not involved
        • Group IV
        • Total head involvement
    • Salter-Thompson Calssification
        • Salter-Thompson classification
        • <i>Based on radiographic crescent sign</i>
        • Class A
        • Crescent sign involves < 1/2 of femoral head
        • Class B
        • Crescent sign involves > 1/2 of femoral head
    • Stulberg classification
      • Gold standard for rating residual femoral head deformity and joint congruence
      • Recent studies show poor interobserver and intraobserver reliability
  • Presentation
    • Symptoms
      • insidious onset
      • may cause painless limp
      • intermittent hip, knee, groin or thigh pain
    • Physical exam
      • hip stiffness
        • loss of internal rotation and abduction
      • gait disturbance
        • antalgic limp
        • Trendelenburg gait (head collapse leads to decreased tension of abductors)
      • limb length discrepancy is a late finding
        • hip adduction contracture can exacerbate the apparent LLD
  • Imaging
    • Radiographs
      • AP of pelvis and frog leg laterals
        • critical in diagnosis and prognosis
      • early findings include
        • medial joint space widening (earliest) from less ossification of head
          • measured between teardrop and ossification center
        • irregularity of femoral head ossification
          • decreased size of ossification center
          • sclerotic appearance
        • crescent sign (represents a subchondral fracture)
    • Bone scan
      • can confirm suspected case of LCPD
        • decreased uptake (cold lesion) can predate changes on radiographs
      • provides information on extent of femoral head involvement
    • MRI
      • early diagnosis revealing alterations in the capital femoral epiphysis and physis
      • more sensitive than radiograph
    • Perfusion studies predict maximum extent of lateral pillar involvement
    • Arthrogram
      • a dynamic arthrogram can demonstrate coverage and containment of the femoral head
  • Studies
    • Histology
      • femoral epiphysis and physis exhibit areas of disorganized cartilage with areas of hypercellularity and fibrillation
  • Differential
    • Radiographic differential diagnosis
      • infection
        • septic arthritis, osteomyelitis, pericapsular pyomyositis
      • transient synovitis
      • multiple epiphyseal dysplasia (MED)
      • spondyloepiphyseal dysplasia (SED)
      • sickle cell disease
      • Gaucher disease
      • hypothyroidism
      • Meyers dysplasia
  • Treatment
    • Goals
      • resolution of symptoms
        • NSAIDs, traction, crutches
      • restoration of range of motion
        • physical therapy (may exacerbate symptoms), muscle lengthenings, Petrie casting
      • containment of hip
        • improve range of motion, bracing, proximal femoral osteotomy, pelvic osteotomy
          • ensure that femoral head is well seated in acetabulum
    • Nonoperative
      • observation alone, activity restriction (non-weightbearing), and physical therapy (ROM exercises)
        • indications
          • children < 8 years of age (bone age <6 years)
            • young patients typically do not benefit from surgery
          • lateral pillar A involvement
        • technique
          • activity restriction and protected weight-bearing during earlier stages until reossification is complete
          • main goals of treatment are to keep the femoral head contained and maintain good motion
            • containment limits deformity and minimizes loss of sphericity
              • lessen subsequent degenerative changes
          • bracing and casting for containment have not been found to be beneficial in a large, prospective study
          • all patients require periodic clinical and radiographic followup until completion of disease process
        • outcomes
          • good outcomes correlate with a spherical femoral head
            • 60% do not require operative intervention
            • good outcomes associated with lateral pillar A and Catterall I groups
    • Operative
      • femoral and/or pelvic osteotomy
        • indications
          • children > 8 years of age, especially lateral pillar B and B/C
        • technique
          • proximal femoral varus osteotomy
            • to provide containment
          • pelvic osteotomy
            • Salter or triple innominate osteotomy
            • Shelf arthroplasty may be performed to prevent lateral subluxation and resultant lateral epiphyseal overgrowth
        • outcomes
          • children with lateral pillar A and those with B under 8 years did well regardless of treatment
          • large recent studies show improved outcomes with surgery for lateral pillar B and B/C in children > 8 years (bone age >6 years)
          • studies sugggest earlier surgery before femoral head deformity develops may be best
          • poor outcome for lateral pillar C regardless of treatment
      • valgus and/or shelf osteotomies
        • indications
          • hinge abduction
            • lateral extrusion of the capital femoral epiphysis producing a painful hinge effect on the lateral acetabulum during abduction
        • abduction-extension osteotomy
          • reposition the hinge segment away from the acetabular margin
          • correct shortening from fixed adduction
          • improve abductor mechanism by improving abductor muscle contractile length
        • Shelf or Chiari osteotomies are also considered when the femoral head is no longer containable
      • hip arthroscopy
        • emerging treatment modality for mechanical abnormalities in the setting of healed LCPD
          • femoroacetabular impingement
      • hip arthrodiastasis
        • indications
          • controversial indications and outcomes
        • technique
          • hip distraction via external fixation
  • Technique
    • Proximal Femoral Varus Osteotomy (VRDO)
      •  indications
        • extrusion in early stages of LCPD
      • technique
        • reposition femoral head into acetabulum for containment purposes
  • Complications
    • Femoral head deformity
      • coxa magna
        • widened femoral head
      • coxa plana
        • flattened femoral head
      • important prognostic factor
        • Stulberg classification
    • Lateral hip subluxation (extrusion)
      • associated with poor prognosis
        • can lead to hinge abduction
    • Premature physeal arrest
      • trochanteric overgrowth
      • coxa breva
        • shortened femoral neck
      • leg length discrepancy
        • typically mild
    • Acetabular dysplasia
      • poor development secondary to deformed femoral head
      • can alter hip congruency
    • Labral injury
      • secondary to femoral head deformity
        • femoroacetabular impingement
    • Osteochondritis dissecans
      • can lead to loose fragments
    • Degenerative arthritis
      • Stulberg I and most Stulberg II hips perform well for the lifetime of the patient
  • Prognosis
    • Important prognostic variables
      • younger age (bone age) < 6 years at presentation is most important good prognostic indicator
      • sphericity of femoral head and congruency at skeletal maturity (Stulberg classification)
      • lateral pillar classification
    • Variables of poor prognosis
      • female sex
      • decreased hip abduction (adduction contracture)
      • heavy patient
      • longer duration from onset to completion of healing
      • stiffness with progressive loss of ROM
      • Catterall "head at risk" signs (see under classification)
    • Natural history
      • long-term studies suggest that most patients do well until fifth or sixth decade of life
      • approximately 1/2 of patients develop premature osteoarthritis secondary to an aspherical femoral head
    • Self-limiting process
      • variable course to final healing from initial ischemic event
      • can take 2-5 years to resolve
    • Differentiated from adult osteonecrosis by its ability to heal and remodel
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