Common Pediatric Lower Limb Disorders

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Presentation transcript:

Common Pediatric Lower Limb Disorders Dr.Kholoud Al-Zain Assistant Professor Consultant, Pediatric Orthopedic Surgeon Dec- 2016 Acknowledgement: Dr.Abdalmonem Alsiddiky Dr.Khalid Bakarman Prof. M. Zamzam

Topics to Cover In-toeing Genu (varus & valgus), & proximal tibia vara Club foot L.L deformities in C.P patients Limping & leg length inequality Leg aches

1) Intoeing

Intoeing- Evaluation Detailed history Onset, who noticed it, progression Fall a lot How sits on the ground Screening examination (head to toe) Pathology at the level of: Femoral anteversion Tibial torsion Forefoot adduction Wandering big toe

Intoeing- Asses rotational profile Pathology Level Special Test Femoral anteversion Tibial torsion Forefoot adduction Wandering big toe Hips rotational profile: Supine Prone Inter-malleolus axis: Foot thigh axis Heel bisector line

Intoeing- Special Test Foot Propagation Angle  normal is (-10°) to (+15°)

Intoeing- Femoral Anteversion Hips rotational profile, supine  IR/ER normal = 40-45/45-50°

Intoeing- Femoral Anteversion Hips rotational profile  prone

Intoeing- Tibial Torsion Inter-malleolus axis Supine position Sitting position Inter-malleolus axis

Intoeing- Tibial Torsion Foot Thigh Axis  normal (0°) to (-10°)

Intoeing- Tibial Torsion Foot Thigh Axis  normal (0°) to (-10°)

Intoeing- Forefoot Adduction Heel bisector line  normal along 2 toe

Intoeing- Adducted Big Toe

Intoeing- Treatment Establish correct diagnosis Parents education Annual clinic F/U  asses degree of deformity Femoral anti-version  sit cross legged Tibial torsion  spontaneous improvement Forefoot adduction  anti-version shoes, or proper shoes reversal Adducted big toe  spontaneous improvement

Intoeing- Treatment Operative correction indicated for children: (> 8) years of age With significant cosmetic and functional deformity  <1%

2) Genu Varus & Valgus

Genu Varum and Genu Valgum Definition: Bow legs Knock knees

Normal Genu Varum and Genu Valgum

Genu Varum and Genu Valgum Types: Physiological is usually  bilateral Pathological  can be unilateral

Genu Varum and Genu Valgum Types: Physiologic Pathologic

Genu Varum and Genu Valgum Evaluation History (detailed) Examination (signs of Rickets) Laboratory Re take the rickets picture

Genu Varum and Genu Valgum Re take the rickets picture

Genu Varum and Genu Valgum

Genu Varum and Genu Valgum Evaluation: Imaging Rickets Put mechanical axsis

Genu Varum and Genu Valgum Management principles: Non-operative: Physiological  usually Pathological  must treat underlying cause, as rickets Epiphysiodesis Corrective osteotomies

“Proximal Tibia Vara”

Proximal Tibia Vara “Blount disease”: damage of proximal medial tibial growth plate of unknown cause Usually: Overweight Dark skinned Types: Infantile  < 3y of age, & usually early walkers Juvenile  3 -10 y, combination Adolescent  > 10y, & usually unilateral

Blount Disease Bilateral Unilateral Types: Infantile  usually in over weight & early walkers Adolescent  usually over weight & unilateral

Blount Disease Staging:

Blount Disease

Blount Disease MRI is mandatory: When: Why? Sever cases Recurrence Is it physis defect

3) Club Foot

Clubfoot Etiology Postural  fully correctable Idiopathic (CTEV)  partially correctable Secondary (Spina Bifida)  rigid deformity, pt needs workup

Clubfoot Clinical examination Characteristic Deformity : Hind foot: Equinus (Ankle joint) Varus (Subtalar joint) Mid & fore foot: Forefoot Adduction Cavus

Clubfoot

Clubfoot Clinical examination: Deformities don’t prevent walking Calf muscles wasting Internal torsion of the leg Foot is smaller in unilateral affection Callosities at abnormal pressure areas Short Achilles tendon Heel is high and small No creases behind Heel Abnormal crease in middle of the foot

A cosmetically pleasing appearance is also an important goal sought by Clubfoot Management: The goal of treatment for is to obtain a foot that is plantigrade, functional, painless, and stable over time A cosmetically pleasing appearance is also an important goal sought by surgeon and family

Clubfoot Manipulation and serial casts: Validity up to 12 months  soft tissue becomes more tight Technique “Ponseti”  3 stages, weekly basis (usually by 6-8w)

Clubfoot Manipulation and serial casts: Maintaining correction “Dennis Brown Splint”  3-4y old

Clubfoot Manipulation and serial casts: Follow up  watch and avoid recurrence, till 9y old Avoid false correction  by going in sequence When to stop ?  not improving, pressure ulcers All pictures put better / Why only to 12 m / when stop

Clubfoot Indications of surgical treatment: Late presentation (>12 months of age) Complementary to conservative treatment (residual forefoot adduction) Failure of conservative treatment Recurrence after conservative treatment

Clubfoot Types of surgery: Soft tissue

Clubfoot Types of surgery: Bony New pictures

Clubfoot Types of surgery: If sever, rigid, and in an older child New pictures

Clubfoot Types of surgery: If sever, rigid, and in an older child (salvage)

4) L.L Deformities in C.P Patients

Lower Limb Deformities in CP Child C.P is  a non-progressive brain insult that occurred during the peri-natal period. Causes  skeletal muscles imbalance that affects joint’s movements. Can be associated with: Mental retardation (various degrees) Hydrocephalus and V.P shunt Convulsions Its not-un-common

Lower Limb Deformities in CP Child Physiological classification: Spastic Athetosis Ataxia Rigidity Mixed Topographic classification: Monoplegia Diplegia Paraplegia Hemiplegia Bilateral hemiplegia Triplegia Quadriplegia or tetraplegia

Lower Limb Deformities in CP Child Hip Flexion Adduction Internal rotation Knee Ankle Equinus Varus or valgus Gait Intoeing Scissoring

Lower Limb Deformities in CP Child Assessment: Gait

Lower Limb Deformities in CP Child Assessment: Hips

Lower Limb Deformities in CP Child Assessment: Knees

Lower Limb Deformities in CP Child Assessment: Ankles

Lower Limb Deformities in CP Child Management is multidisciplinary: Parents education Pediatric neurology  diagnosis, F/U, treat fits P.T (home & center)  joints R.O.M, gait training Orthotics  maintain correction, aid in gait Social / Government aid Others: Neurosurgery (V.P shunt), Ophthalmology (eyes sequent), …etc.

Lower Limb Deformities in CP Child

Lower Limb Deformities in CP Child Indications of Orthopedic surgery: Sever contractures preventing P.T P.T plateaued due to contractures Perennial hygiene (sever hips adduction) In a non-walker to sit confortable in wheelchair Prevent: Neuropathic skin ulceration (as feet) Joint dislocation (as hip)

Lower Limb Deformities in CP Child Options of Surgery: Tenoplasty Tenotomy Neurectomy Tendon Transfer Bony surgery  Osteotomy/Fusion

5) Limping

Limping Definition Limping  an abnormal gait, Due to: Pain (where), Deformity (bone or joint), or Weakness (general or nerve or muscle) In one or both limbs

Limping Diagnosis by: History (detailed) Examination: Gait good analysis Is it: Above pelvis  Back (scoliosis) Below pelvis  Hips, knees, ankles, & feet Neuro.Vascular

Limping Management: Generalization can’t be made. Treatment of the cause:

If The Cause Was MSK That Led To Limb Length Inequality

Limb Length Inequality True vs. apparent Etiology:

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH Developmental  as Blount’s

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH Developmental  as Blount’s Traumatic  as oblique # (short), or multifragmented (long)

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH Developmental  as Blount’s Traumatic  as oblique # (short), or multifragmented (long) Infection  stunted growth or dissolved part of bone

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH Developmental  as Blount’s Traumatic  as oblique # (short), or multifragmented (long) Infection  stunted growth or dissolved part of bone Metabolic  as rickets

Limb Length Inequality True vs. apparent Etiology: Congenital  as DDH Developmental  as Blount’s Traumatic  as oblique # (short), or multifragmented (long) Infection  stunted growth or dissolved part of bone Metabolic  as rickets (unilateral) Tumor  affecting physis

Limb Length Inequality Adverse effects & clinical picture: Gait disturbance Equinus deformity Pain: back, leg Scoliosis (secondary) Evaluation: Screening examination Clinical measures of discrepancy Imaging methods (Centigram)

Limb Length Inequality Management depends on the severity (>2cm): For shorter limb: Shoe raise Bone lengthening For longer limb: Epiphysiodesis (temporary or permanent) Bone shortening

6) Leg Aches

Leg Aches What is leg aches? “Growing pain” Benign In 15 – 30 % of normal children F > M Unknown cause No functional disability, or limping Resolves spontaneously, over several years Growth spert

Leg Aches Clinical features  diagnosis by exclusion H/O: O/E: At long bones of L.L (Bil) Dull aching, poorly localized Can be without activity At night Of long duration (months) Responds to analgesia O/E: Long bone tenderness  nonspecific, large area, or none Normal joints motion

Leg Aches D.D from serious problems, mainly tumor: Osteoid osteoma Osteosarcoma Ewing sarcoma Leukemia SCA Subacute O.M

Leg Aches Management Reassurance Symptomatic: Analgesia (oral, local) Rest Massage

Any Question ?

Remember

Take Home Message Intoeing  is one of 4 causes, treatment depends on the level, mainly observe, operate >8y old Genu varus & valgus  phys vs. patho, rickets, when operate Blount  early walkers, treatment mainly surgery CTEV  3 types, treat as young as possible, Ponseti better to avoid surgery L.L in C.P  mainly treat spastic, PT importance, surgery indications Limping  due (pain- week- deformed), above or below pelvis L.L.I  proper assess (cause & level), treated >2cm, options of treat Leg aches  symptomatic treatment