Literature DB >> 9591999

Chronic physeal fractures in myelodysplasia: magnetic resonance analysis, histologic description, treatment, and outcome.

W B Rodgers1, R M Schwend, D Jaramillo, J R Kasser, J B Emans.   

Abstract

Thirteen myelodysplastic children with 19 chronic physeal fractures were treated. All were treated with prolonged immobilization (average, 5.8 months; range, 3-18 months) in either braces or casts; four of the fractures required operative fixation to facilitate healing. All were healed at 4.8-years follow-up but, in four of the fractures, the growth plate closed prematurely. Three of the children underwent magnetic resonance imaging (MRI) of the injured physes, and one underwent physeal biopsy as part of her operative epiphysiodesis. Histologic analysis revealed three distinct zones of physeal pathoanatomy: a normal zone of proliferation; a thickened, disorganized zone of hypertrophy; and a vascularized zone of fibrous tissue adjacent to the metaphysis. On MRI, there was thickening of the physis and irregularity of the zone of provisional calcification. The physeal cartilage and the juxtametaphyseal fibrovascular tissue enhanced with gadolinium. These findings corroborate earlier mechanistic proposals for physeal injury in myelodysplasia: chronic stress or trauma to the poorly sensate limb produces micromotion at the zone of hypertrophy, yielding a widened, disorganized physis, and leading to fracture, displacement, and delayed union.

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Year:  1997        PMID: 9591999     DOI: 10.1097/00004694-199709000-00008

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  2 in total

1.  Incidence, prevalence, and characteristics of fractures in children, adolescents, and adults with spina bifida.

Authors:  Nienke P Dosa; Michael Eckrich; Danielle A Katz; Margaret Turk; Gregory S Liptak
Journal:  J Spinal Cord Med       Date:  2007       Impact factor: 1.985

2.  Dramatic subperiosteal bone formation following physeal injury in patients with myelomeningocele.

Authors:  Joseph G Khoury; Jose A Morcuende
Journal:  Iowa Orthop J       Date:  2002
  2 in total

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