Tibia vara
"tibia vara" OR "Blount disease"



| Cause | Features |
|---|---|
| Physiologic bowing | Bilateral, self-resolving, no epiphyseal changes |
| Blount disease | Medial epiphyseal fragmentation, progressive |
| Rickets | Metabolic, bilateral, cupping/fraying of multiple physes |
| Focal fibrocartilaginous dysplasia | Linear radiolucency in proximal tibial metadiaphysis, usually self-resolving |
| Trauma / infection | History, localized changes |
| Neurofibromatosis | Anterolateral bowing, 50-55% of anterolateral tibial bowing |
| Fibrous dysplasia | 15% of anterolateral tibial bowing |
| Ollier disease / Maffucci syndrome | Multiple enchondromas |
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| Feature | Infantile | Adolescent |
|---|---|---|
| Age | <8 years (peak 1-3 yr) | >8 yr, before skeletal maturity |
| Laterality | Bilateral 60% | Mostly unilateral |
| Progression | Progressive | Worsens with time |
| Recurrence after surgery | Less | More |
| Ethnicity | Afro-Caribbean | All groups |

| Stage | Changes |
|---|---|
| I | Irregularity + slight beaking of medial metaphysis |
| II | Beak more pronounced, epiphysis irregular |
| III | Fragmentation of medial epiphysis |
| IV | Depression of medial tibial plateau |
| V | Separation of medial epiphysis |
| VI | Premature fusion of medial physis at 90° downward angle |
| Condition | Key Differentiator |
|---|---|
| Physiologic bowing | 100% bilateral, resolves by age 3, no epiphyseal changes |
| Rickets | Metabolic, cupping/fraying at multiple physes, low vit D |
| Focal fibrocartilaginous dysplasia | Linear radiolucency, usually self-resolving |
| Neurofibromatosis | Anterolateral bowing (not posteromedial) |
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| Section | ✓ Covered |
|---|---|
| Definition | ✅ |
| Aetiology / Pathogenesis | ✅ |
| Classification (Infantile vs Adolescent) | ✅ |
| Pathology | ✅ |
| Langenskiöld 6 Stages (with diagram) | ✅ |
| Clinical Features | ✅ |
| Investigations (X-ray + MRI + Measurements) | ✅ |
| Differential Diagnosis | ✅ |
| Treatment (all 6 options) | ✅ |
| Complications | ✅ |
| High-Yield Exam Points | ✅ |
Complete answer
| Feature | Infantile | Adolescent |
|---|---|---|
| Age of onset | Before 8 yrs (peak 1-3 yrs) | After 8 yrs, before skeletal maturity |
| Laterality | Bilateral 60% | Mostly unilateral |
| Inciting event | None | None |
| Progression | Progressive | Worsens with time |
| Recurrence post-op | Less | More (higher recurrence) |
| Ethnicity | Afro-Caribbean dominant | All groups |

| Stage | Radiological Change |
|---|---|
| I | Irregularity + slight medial metaphyseal beaking |
| II | Beak more pronounced, epiphysis becomes irregular |
| III | Fragmentation of medial epiphysis |
| IV | Depression of medial tibial plateau |
| V | Separation of medial epiphyseal portion |
| VI | Premature medial physeal fusion at 90° downward angle |
At Stage VI: medial physis fuses completely → no further growth correction possible

| Measurement | Significance |
|---|---|
| Metaphyseal-Diaphyseal (Drennan) Angle >11° | Most important early indicator |
| Tibiofemoral angle | Most functional measure of deformity |
| Mechanical axis deviation | Overall limb alignment assessment |
| Fibula length vs tibia | Early indicator |
Drennan angle = angle between line through metaphyseal beaks (transverse tibial metaphysis axis) and perpendicular to longitudinal tibial axis
| Condition | Key Differentiator |
|---|---|
| Physiologic bowing | 100% bilateral, resolves by age 2-3, no epiphyseal changes |
| Rickets | Metabolic, bilateral, cupping/fraying multiple physes, low vitamin D/phosphate |
| Focal fibrocartilaginous dysplasia | Linear radiolucency at proximal tibial metadiaphysis, self-resolving |
| Neurofibromatosis type 1 | Anterolateral tibial bowing (NOT posteromedial), 50-55% of anterolateral bowing |
| Fibrous dysplasia | 15% of anterolateral tibial bowing |
| Ollier disease / Maffucci | Multiple enchondromas |
| Trauma / infection | History, localized changes |
| SCFE | Similar histology, hip involvement |
Posteromedial bowing = usually physiologic, resolves spontaneously Anterolateral bowing = associated with NF1 and fibrous dysplasia
| Type | Description |
|---|---|
| Rab oblique osteotomy | Corrects varus + internal rotation simultaneously; postoperative cast wedging possible |
| Greene crescent (chevron) osteotomy | Opening-closing wedge; maintains limb length |
| Zayer hemicondylar osteotomy | Through epiphysis into intercondylar notch; corrects posteromedial tibial plateau slope |
| Ingram-Canale-Beaty epiphyseal + metaphyseal osteotomy | For advanced deformity |
| Device | Indication |
|---|---|
| Uniplanar external fixator | Isolated frontal-plane deformity; allows lengthening, avoids second operation |
| Ilizarov fixator | Adolescents; deformity correction + simultaneous tibial lengthening |
| Hexapod / Taylor Spatial Frame | Obese adolescents with multiplanar deformity; computer-navigated correction |
| Point | Value |
|---|---|
| Pathognomonic X-ray sign | Medial metaphyseal fragmentation |
| Most important early indicator | Drennan (MD) angle >11° |
| Langenskiöld final stage | Stage VI = fusion at 90° downward |
| Osteotomy before age 4 | Recurrence <20% |
| Osteotomy after age 4 | Recurrence 80-90% |
| Clinical sign | Sharp proximal tibial angulation (NOT smooth) |
| Does NOT occur in | Non-ambulatory children |
| Infantile bilateral % | 60% (physiologic = 100%) |
| Adolescent form | Higher recurrence than infantile |
| Unilateral disease → after correction | Limb is short → consider tibial lengthening |
| Femoral varus in late-onset | ~10° more than ideal = 34-76% of total deformity |
| Common post-op complication | Peroneal nerve palsy + compartment syndrome |