Osteochondroses - David Houlihan-Burne 4/3/2002BLOUNT’S DISEASE
Causes - Physiological, Osteogenesis imperfecta, osteochondromas, metabolic aberrations, trauma, dysplasis (especially focal fibrocartilaginous dysplasia), Blount’s
Physiological bowing (normal in <2yrs) v. Blount’s
Blount’s disease (aka Tibia vara , osteochondrosis deformans) –rare,
disorder of
posterior medial tibial physes.
Varus, internal torsion and genu recurvatum
Erlacher 1922, Blount 1937 (
JBJS 19:1-29, 1937)
Infantile (< 3yr) v Adolescent
v Juvenile (6-9)
( added by Thompson
in 1984)
Infantile is usually bilateral (60%) and associated with internal tibial torsion
Adolescent is unilateral and less severe (is pathologically compared with SUFE)
Aetiology
Histology
Not AVN
Staging
(Langenskiold and Riska) I-VI – (Based on 17 cases in 1952)
Radiographs
Treatment
Based on age and stage of disease
Racial group can affect outcome
Infantile Blount’s
< 3 yrs old
Bracing (HKAFO). Overcorrect to valgus. If neutral TibFem axis not achieved after
1 yr then HTO.
> 4 yrs old
HTO (Rab oblique osteotomy) to correct varus and int. rotation (overcorrect)
(
J Paed Orthop 8:717, 1988)
Also Chevron, intraepiphyseal, epiphyseal and metaphyseal
Plating for older children. Also x-fix, Iliozarov, combined HTO and med plateau elevation.
Adolescent
Alignment procedure – Plating, x-fix, ilizarov. Lateral epipysiodesis
Often distal femur needs addressing with valgus osteotomy
Treatment Summary
Recurrence rate
High in juvenile type, absent in adolescent type (
J Paed Orthop 4:185-194:1984)
Up to 75 % in children > 5 yrs old having HTO
crt 30 % if done at younger age
In infantile group the older you are the higher recurrence and the more operations required to correct deformity
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