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Lower limb deformities
• Coxa vara
Coxa vara is a deformity of the hip, whereby
the angle between the head and the shaft of
the femur is reduced to less than 120 degrees.
 Features
• shortening of limb
• limp.
• bilateral involvement….waddling gait
• Restricted abduction and internal rotation
 Causes
• Congenital
• Pathological. metabolic bone diseases (e.g. Paget's
disease of bone), post-Perthes deformity,
osteomyelitis,
• Traumatic
Diagnosis
• X Ray
HE angle
Treatment
• HE angle of 45–60 degrees: observation and
periodic follow up
Indication for surgery
• HE angle more than 60 degrees, progressive
deformity, neckshaft angle <90 degrees,
development of Trendelenburg gait
Surgery
• subtrochanteric valgus osteotomy with
adequate internal rotation of distal fragment
to correct anteversion
Complications
• Recurrence
Coxa valga
• Coxa valga describes a deformity of the hip
where there is an increased angle between
the femoral neck and femoral shaft.
• Coxa valga is often associated with shallow
acetabular angles and femoral head
subluxation.
• Etiology
bilateral
• neuromuscular disorders, e.g. cerebral palsy
• often have concurrent femoral anteversion
• skeletal dysplasias, e.g. Turner syndrome,
mucopolysaccharidoses
unilateral
• trauma causing growth plate arrest
• Diagnosis
• X ray
Treatment
• Coxa valga can be treated with varus
derotation osteotomy (VDRO) and angled
blade-plate fixation
Femoral Retroversion
• Common in early infancy
• Unilateral, R side > L side
• More common in obese children
• apparent when the pre-walking child stands
with his or her feet turned out to nearly 90
degrees ("Charlie Chaplin appearance")
• It may gradually improve on its own during
the first year of walking
Hallux valgus
• Hallux valgus is deviation of the
big toe away from the midline,
i.e. towards the lesser toes, and is
usually associated with a bunion.
• affects women more than men
• Often bilateral
• Inherited
• fully enclosed shoes accelerate
the development
Complications
2nd MTP overloading and dislocations
Treatment options.
• Non-operative. Wider toe box and pressure
relief.
• Operative.
I. Mild deformities. distal osteotomy (e.g.
chevron)
I.
II. Moderate deformities.
Scarf or Ludloff, or a basal
(proximal chevron or
crescentic) osteotomy.
III. Severe deformities.
Osteotomies or fusion of
1st TM or MTP Joints
Complications of surgery.
• Infection
• Cutaneous nerve damage
• Recurrence or overcorrection of deformity
• Stiffness and overload of the second MTP
joint.
• Arthritis
Hallux rigidus
• Hallux rigidus is a painful condition of the
hallux MTP joint
• characterised by loss of motion especially in
dorsiflexion.
• osteophyte formation on the dorsum and
sides of the joint.
• trauma or repetitive microtrauma (sport)
• strong family history
• Patients complain of stiffness and pain on
weight bearing.
• Non-operative treatment. Provision of a stiff-
soled shoe with a deep toe box or a rocker-soled
shoe.
• Surgical management.
• injection/manipulation,
• cheilectomy (a radical debridement and excision
of the part of the joint blocking movement)
• fusion
• Arthroplasty (Keller’s-type procedure or silicon
interposition)
Congenital talipes equinovarus
(CTEV) (the ‘club foot’)
• Multiplanar deformity: hindfoot equinus and
varus, midfoot adductus and forefoot cavus
• Incidence is 1–6 per 1000 live births, more
common in boys and with a familial tendency
• Most cases are idiopathic but neuromuscular
causes include spina bifida and arthrogryposis
• Scoring systems (Pirani/Dimeglio), are used to
assess the severity
• The diagnosis of CTEV may be made during an
antenatal ultrasound.
• Pathology
• Types
• Postural
• Idiopathic
• Neuromuscular i.e Spina bifida;
arthrogryposis;
• Syndromic Trisomy 15
Treatment
• PONSETI METHOD
• corrects foot deformity in 95% of idiopathic
cases without the need for a formal surgical
release.
• Manual repositioning
• Series of well moulded above-knee plaster
casts.
• Foot abduction orthosis (FAO)
• Percutaneous Achilles tenotomy
• Recurrent deformity can be treated with
further plasters,but a tibialis anterior tendon
transfer may be required around the age of
2.5–4
• Feet treated with the Ponseti method are less
stiff, less likely to be painful and less subject to
overcorrection than those treated surgically.
SURGICAL TREATMENT
• When conservative treatment fails, surgical
intervention is required, ideally before walking
age.
• sequential release of the pathologically tight
structures via either a Turco incision or the
Cincinnati incision.
• Stiffness and over or undercorrection are
common complications
Talipes calcaneovalgus (TCV)
• Calcaneovalgus Foot is a common acquired
condition caused by intrauterine "packaging"
seen in neonates that presents as a benign
soft tissue contracture deformity of the foot
characterized by hindfoot eversion and
dorsiflexion.
• Diagnosis is made clinically
• Treatment is usually observation with passive
stretching and possible casting as the
condition resolves spontaneously in 3-6
months.
Lower limb deformities.pptx

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Lower limb deformities.pptx

  • 2. • Coxa vara Coxa vara is a deformity of the hip, whereby the angle between the head and the shaft of the femur is reduced to less than 120 degrees.
  • 3.
  • 4.  Features • shortening of limb • limp. • bilateral involvement….waddling gait • Restricted abduction and internal rotation  Causes • Congenital • Pathological. metabolic bone diseases (e.g. Paget's disease of bone), post-Perthes deformity, osteomyelitis, • Traumatic
  • 6. Treatment • HE angle of 45–60 degrees: observation and periodic follow up Indication for surgery • HE angle more than 60 degrees, progressive deformity, neckshaft angle <90 degrees, development of Trendelenburg gait
  • 7. Surgery • subtrochanteric valgus osteotomy with adequate internal rotation of distal fragment to correct anteversion Complications • Recurrence
  • 8. Coxa valga • Coxa valga describes a deformity of the hip where there is an increased angle between the femoral neck and femoral shaft. • Coxa valga is often associated with shallow acetabular angles and femoral head subluxation.
  • 9. • Etiology bilateral • neuromuscular disorders, e.g. cerebral palsy • often have concurrent femoral anteversion • skeletal dysplasias, e.g. Turner syndrome, mucopolysaccharidoses unilateral • trauma causing growth plate arrest
  • 10. • Diagnosis • X ray Treatment • Coxa valga can be treated with varus derotation osteotomy (VDRO) and angled blade-plate fixation
  • 11. Femoral Retroversion • Common in early infancy • Unilateral, R side > L side • More common in obese children • apparent when the pre-walking child stands with his or her feet turned out to nearly 90 degrees ("Charlie Chaplin appearance") • It may gradually improve on its own during the first year of walking
  • 12.
  • 13. Hallux valgus • Hallux valgus is deviation of the big toe away from the midline, i.e. towards the lesser toes, and is usually associated with a bunion. • affects women more than men • Often bilateral • Inherited • fully enclosed shoes accelerate the development
  • 14. Complications 2nd MTP overloading and dislocations Treatment options. • Non-operative. Wider toe box and pressure relief. • Operative. I. Mild deformities. distal osteotomy (e.g. chevron)
  • 15. I. II. Moderate deformities. Scarf or Ludloff, or a basal (proximal chevron or crescentic) osteotomy. III. Severe deformities. Osteotomies or fusion of 1st TM or MTP Joints
  • 16. Complications of surgery. • Infection • Cutaneous nerve damage • Recurrence or overcorrection of deformity • Stiffness and overload of the second MTP joint. • Arthritis
  • 17. Hallux rigidus • Hallux rigidus is a painful condition of the hallux MTP joint • characterised by loss of motion especially in dorsiflexion. • osteophyte formation on the dorsum and sides of the joint.
  • 18.
  • 19. • trauma or repetitive microtrauma (sport) • strong family history • Patients complain of stiffness and pain on weight bearing.
  • 20. • Non-operative treatment. Provision of a stiff- soled shoe with a deep toe box or a rocker-soled shoe. • Surgical management. • injection/manipulation, • cheilectomy (a radical debridement and excision of the part of the joint blocking movement) • fusion • Arthroplasty (Keller’s-type procedure or silicon interposition)
  • 21. Congenital talipes equinovarus (CTEV) (the ‘club foot’) • Multiplanar deformity: hindfoot equinus and varus, midfoot adductus and forefoot cavus • Incidence is 1–6 per 1000 live births, more common in boys and with a familial tendency • Most cases are idiopathic but neuromuscular causes include spina bifida and arthrogryposis • Scoring systems (Pirani/Dimeglio), are used to assess the severity
  • 22.
  • 23. • The diagnosis of CTEV may be made during an antenatal ultrasound.
  • 25.
  • 26. • Types • Postural • Idiopathic • Neuromuscular i.e Spina bifida; arthrogryposis; • Syndromic Trisomy 15
  • 27. Treatment • PONSETI METHOD • corrects foot deformity in 95% of idiopathic cases without the need for a formal surgical release. • Manual repositioning • Series of well moulded above-knee plaster casts.
  • 28.
  • 29. • Foot abduction orthosis (FAO) • Percutaneous Achilles tenotomy • Recurrent deformity can be treated with further plasters,but a tibialis anterior tendon transfer may be required around the age of 2.5–4
  • 30. • Feet treated with the Ponseti method are less stiff, less likely to be painful and less subject to overcorrection than those treated surgically.
  • 31. SURGICAL TREATMENT • When conservative treatment fails, surgical intervention is required, ideally before walking age. • sequential release of the pathologically tight structures via either a Turco incision or the Cincinnati incision.
  • 32.
  • 33. • Stiffness and over or undercorrection are common complications
  • 34. Talipes calcaneovalgus (TCV) • Calcaneovalgus Foot is a common acquired condition caused by intrauterine "packaging" seen in neonates that presents as a benign soft tissue contracture deformity of the foot characterized by hindfoot eversion and dorsiflexion.
  • 35.
  • 36. • Diagnosis is made clinically • Treatment is usually observation with passive stretching and possible casting as the condition resolves spontaneously in 3-6 months.