- Also known as
- Anterolateral bowing
Definition
- Anterolateral bowing.
- True bone dysplasia with non union or potential non union through a hamartomatoUsually area in the tibia.
- not present at birth
- really a fibrous non-union of a pathological fracture
- The defect in the bone is filled with mature, fibrous connective tissue.
- The name is, therefore, a misnomer since, by definition, a pseudarthrosis has a cleft lined by fibrocartilage containing fluid and bounded by a capsule.
- Bowing usually at junction of Mid / Distal 1/3
Epidemiology
- Rare
- 1:200 000
- M = F
- 50% have Neurofibromatosis type 1
- 1-3% of Neurofibromatosis have CPT
Aetiology
- Cause unknown
- Theories include:
- Intrauterine fracture
- Localised vascular abnormality
- Constriction due to proliferating fibrous tissue
- Localised lesions Eg fibrous Dysplasia
Pathology
- HamartomatoUsually cuff present at site of lesion site
- Even with Neurofibromatosis, no clear histol evidence that fibrous tissue is Neurofibromatosis
Classification
Type | Description |
---|---|
1 Non-dysplastic | ~Increased cortical density ~Dense medullary canal |
2 Dysplastic | |
a | ~Wide medullary canal ~Failure of tubulation |
b | ~Cystic lesion before fracture or canal enlargement from a previous fracture |
c | ~Fracture, Cysts & Frank pseudarthrosis; Narrowed ends of fragments |
Type | Description |
---|---|
1 | ~Congenital anterior bowing ~Defect present in tibia on x-ray ~Other Congenital defects may be present ~Rare |
2 | ~Congenital anterior bowing ~Hourglass constriction of tibia ~Spontaneously fracture or 2° minor trauma ~Usually < 2 yrs when fracture ~Tapered, rounded & sclerotic ~Medial cavity on XR ~Most commmon & worst prognosis ~Prognosis worse with Neurofibromatosis ~1/2 of cases |
3 | ~Fracture develops at site of bone cyst ~Usually near junction of mid/ distal 1/3 ~Anterior bowing precedes or follow fracture |
4 | ~Sclerotic bony segment initially present at junction of mid/ distal 1/3 ~Segment may produce complete or partial obliteration of medial canal ~No narrowing of tibia ~Fracture develops like stress fracture |
5 | ~Congenital dysplastic tibia ~Mild bowing ~ ± Pseudarthrosis |
6 | ~Intraosseous Neurofibromatosis or Schwannoma ~± Pseudarthrosis ~Very rare |
Natural History
- If have Neurofibromatosis – virtually all will fracture by 2y
- reasonable to bypass graft prophylactically involved segment if has Neurofibromatosis
Management
- No fracture ie Type I or IIA
- brace all
- If have Neurofibromatosis -> discuss prophylactic bypass graft +/- excision
- Fracture ie Type II B&C
- usually excise segment, graft & rod
- several options with rod
- Sheffield growing rod through ankle joint
- Steinman pins etc in tibia
- 40-80% success
- Difficult to treatment
- Won’t heal by POP alone
- Pre fracture treatment = Preventative bracing
- After fracture, treatment is surgical
- Usually ~ 2yo
- Try to avoid surgery till older
- problem is one of malalignment & ongoing stress riser
- Surgery Timing Controversial
- More delay = shorter underdeveloped leg
- Older pt = Increased union rate
- ? Brace till large enough or first controlled by AFO & then surgery
- Bone Grafting
- Can be done prophylactically in concavity of bowed tibia
- In combination
- IM Rod
- First approach once fractured
- Most reliable technique
- 60% union rate
- Vascularised Free Fibular Graft
- Pseudarthrosis segment resected
- Contralateral fibula unless Ipsilateral Fibula OK
- Hold with Ilizarov or External Fixateur
- Good results reported ~ 80%
- Advantages:
- 1° bone lengthening
- Defect correction
- Rapid union
- Disadvantages
- Tech demanding
- Requires microsurgery
- Operation on normal leg
- Major problem is valgus
- Usually defects of Normal ankle joint 2° overgrowth of distal tibial epiphysis
- Distal fibula acts as tether
- Treatment with tibial / Fibular synostosis
- Avoid by using ipsilateral fibula
- Only possible if fibula not involved
- Ilizarov Tech
- Pseudarthrosis resected
- Corticotomy of proximal metaphysis performed
- 3-level ring fixator applied
- Middle tibial segment moved distally to provide metaphyseal lengthening & Pseudarthrosis compression
- Allows: Bone lengthening
- Correct of defect
- High union rates
- Amputation
- “hould not be the operation of first resort or last resort
- Several lesions with poor prognosis
- Make early decision
- Boyd or Syme have excellent outcome in this group
Prognosis
- Varies by type
- Worse with
- Congenital / early onset
- Shortening
- Tapering
- Sclerosis
- Failure of surgery with graft resorption
- Amputation in 50%
- Remember 25% of patients with Neurofibromatosis1 develop CNS Glioma
- Coast of Maine café au lait spots (irreg outline)
- associated with Albright’s syndrome
- Triad
- precocious puberty
- polyostotic fibrous dysplasia
- café au lait spots
- Triad
- Malignant transformation rate – 4% of fibrous dysplasia
- Malignant transformation rate in fibrous dysplasia is <1%
- Coast of California (smooth outline)
- café au lait spots associated with neurofibromatosis