Salter-Harris type IV fracture
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Salter-Harris type IV fractures are relatively uncommon injuries that occur in children. They are intra-articular injuries in which the fracture extends through the epiphysis, across the physis, and through the metaphysis. Salter-Harris fractures are a group of childhood injuries where a fracture involves the physis.
Salter-Harris IV injuries typically have a poor prognosis due to interruption of the proliferative and reserve cartilage zones often leading to altered joint mechanics and functional impairment and as such orthopedic evaluation and subsequent operative intervention are often required 1,2.
Approximately 10-12% of all physeal fractures will be a Salter-Harris type IV fracture. Salter-Harris type IV injuries will often follow typical location patterns and most commonly involve the distal radius, phalanges, and distal tibia.
lucent fracture line extending through the metaphysis, across physis, and into the epiphysis
angulation, displacement, and rotation may occur
adjacent soft tissue swelling and joint effusion may be noted
CT may be helpful to further assess the nature of the fracture. This is particularly helpful in the distal tibia when the plain film can under-estimate the complexity and severity of a distal tibial injury.
CT imaging has a role in evaluating the degree of displacement and anatomic extent of Salter-Harris type IV fractures and can subsequently guide operative intervention
CT imaging can also be incorporated to evaluate focal osseous bridging across the physis during the healing process (most common in Salter-Harris IV and V injuries) 3
- 1. Levine R, Thomas A, Nezwek T, Waseem M. Salter-Harris Fracture. 2023. - Pubmed
- 2. Cepela D, Tartaglione J, Dooley T, Patel P. Classifications In Brief: Salter-Harris Classification of Pediatric Physeal Fractures. Clin Orthop Relat Res. 2016;474(11):2531-7. doi:10.1007/s11999-016-4891-3 - Pubmed
- 3. Nguyen J, Markhardt B, Merrow A, Dwek J. Imaging of Pediatric Growth Plate Disturbances. Radiographics. 2017;37(6):1791-812. doi:10.1148/rg.2017170029 - Pubmed