Literature DB >> 11499786

Focal fibrocartilaginous dysplasia: curettage as an alternative to conservative management or more radical surgery.

G Khanna1, M Sundaram, G Y El-Khoury, K Merkel.   

Abstract

We describe two cases of focal fibrocartilaginous dysplasia, one treated conservatively while the other underwent curettage of the lesion. Resolution of tibia vara and healing of the focal fibrocartilaginous dysplasia was noted at 6 months in the patient who underwent curettage while the conservatively managed patient required 8 years of follow-up. Of the 17 cases of conservatively followed tibial focal fibrocartilaginous dysplasia described in the literature, 11 showed complete recovery after a median interval of 57 months. We believe that curettage may result in rapid healing by removing the persistent mesenchymal anlage which can interfere with the normal growth of the tibia.

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Year:  2001        PMID: 11499786     DOI: 10.1007/s002560100359

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  2 in total

1.  Unilateral tibia vara in a toddler caused by focal fibrocartilaginous dysplasia.

Authors:  Kristina Imeen Ringe; Eckart Schirg; Herbert Rosenthal; Hans Berendonk; Michael Galanski
Journal:  J Radiol Case Rep       Date:  2009-09-01

2.  The natural history of focal fibrocartilaginous dysplasia in the young child with tibia vara.

Authors:  Vito Pavone; Gianluca Testa; Maria Riccioli; Andrea Sessa; Francesco Roberto Evola; Sergio Avondo
Journal:  Eur J Orthop Surg Traumatol       Date:  2013-10-29
  2 in total

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