Contents

SynopsisCodesLook ForDiagnostic PearlsDifferential Diagnosis & PitfallsBest TestsManagement PearlsTherapyReferences

View all Images (3)

Infantile Blount disease
Other Resources UpToDate PubMed

Infantile Blount disease

Contributors: Aron Sulovari BA, Sandeep Mannava MD, PhD
Other Resources UpToDate PubMed

Synopsis

Causes / typical injury mechanism: The exact etiology of infantile Blount disease is unknown. Spontaneous deceleration of growth can occur at the posteromedial proximal tibial physis, resulting in varus deformity or relative tibial shortening in unilateral cases.

Classic history and presentation: Infantile Blount disease is characterized by varus deformity of the proximal tibia. Approximately 50% of the cases are bilateral but not symmetric.

Prevalence:
  • Age – Most common in children aged 2-5 years.
  • Sex / gender – More common in boys than girls.
Risk factors: Risk factors for infantile Blount disease are early walking age, obesity, and vitamin D deficiency.

Pathophysiology: The exact etiology of infantile Blount disease is unknown. Histological evidence suggests replacement of physeal cartilage by fibrous tissue or physeal arrest between the epiphysis and metaphysis.

Grade / classification system:
Langenskiold Classification of Blount disease

Stage I (2-3 years of age)
Medio-distal beaking of the upper proximal tibial metaphysis.

Stage II (2.5-4 years of age)
Wedging of the medial part of the upper tibial epiphyseal secondary ossification center plus a saucer-shaped defect of the upper surface of the metaphyseal beak due to its dissolution, fragmentation, and collapse.

Stage III (4-6 years of age)
Stepping of the inferior-medial border of the secondary ossification center but without extending distally to the physeal plate level, plus deepening of the metaphyseal saucer into a step in the medial metaphysis.

Stage IV (5-10 years of age)
The epiphyseal secondary ossification center passes more distally and crosses distal to the physeal level to fill the metaphyseal step.

Stage V (9-11 years of age)
Separation of the most medial part of the ossification center from the bulk of the secondary ossification center to reside in the depth of the metaphyseal step below the physis. This is radiologically expressed as either a horizontal cleft (double epiphysis) or complete absence of the medial secondary ossification center as it will be overshadowed by the upper medial tibial metaphysis.

Stage VI (0-13 years of age)
Medial epiphyseal plate closure with a bony bridge.

Related topic: adolescent Blount disease

Codes

ICD10CM:
M92.519 – Juvenile osteochondrosis of proximal tibia, unspecified leg

SNOMEDCT:
880067009 – Blount disease

Look For

Subscription Required

Diagnostic Pearls

Subscription Required

Differential Diagnosis & Pitfalls

Best Tests

Subscription Required

Management Pearls

Subscription Required

Therapy

Subscription Required

References

Subscription Required

Last Reviewed:08/29/2021
Last Updated:01/27/2022
Copyright © 2022 VisualDx®. All rights reserved.
Infantile Blount disease
Copyright © 2022 VisualDx®. All rights reserved.