Literature DB >> 31331926

Pathological fracture of non-ossifying fibroma associated with neurofibromatosis type 1.

James Ritchie Gill1, Tamer Magid El Nakhal1, Soo-Mi Park2, Mariusz Chomicki1.   

Abstract

We report the management of a pathological fracture through a proximal tibial non-ossifying fibroma (NOF) in a 13-year-old girl with neurofibromatosis type 1 (NF1). The fracture was minimally displaced, and the lesion had clinical features of a NOF, and therefore biopsy was not required. Operative fixation has been the preferred method of treatment for pathological fractures through NOF associated with NF1. Multiple NOFs associated with NF1 are rare but can coalesce resulting in large lesions with an increased risk of pathological fracture. In cases which permit, non-operative treatment with cast immobilisation can yield satisfactory results. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  accidents; injuries; knee injuries; orthopaedics

Mesh:

Year:  2019        PMID: 31331926      PMCID: PMC6663272          DOI: 10.1136/bcr-2018-228170

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  20 in total

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9.  Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder.

Authors:  Douglas R Stewart; Hilde Brems; Alicia G Gomes; Sarah L Ruppert; Tom Callens; Jennifer Williams; Kathleen Claes; Michael B Bober; Rachel Hachen; Leonard B Kaban; Hua Li; Angela Lin; Marie McDonald; Serge Melancon; June Ortenberg; Heather B Radtke; Ignace Samson; Robert A Saul; Joseph Shen; Elizabeth Siqveland; Tomi L Toler; Merel van Maarle; Margaret Wallace; Misti Williams; Eric Legius; Ludwine Messiaen
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Authors:  Stéphane Cherix; Yann Bildé; Fabio Becce; Igor Letovanec; Hannes A Rüdiger
Journal:  BMC Musculoskelet Disord       Date:  2014-06-26       Impact factor: 2.362

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  1 in total

1.  Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.

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  1 in total

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