Literature DB >> 9587756

Multiple lower limb non-ossifying fibromas in siblings with neurofibromatosis.

D C Howlett1, M M Farrugia, R E Ferner, S C Rankin.   

Abstract

Non-ossifying fibromas are common benign lesions of tubular long bones. There is recognized association of these bony lesions with neurofibromatosis type 1 although the presence of non-ossifying fibromas in familial members with the condition has not previously been reported. We report two siblings with neurofibromatosis and radiological evidence of multiple lower limb non-ossifying fibromas. Both patients presented with pain in the knees and a pathological fracture was observed in one case. Patients with multiple non-ossifying fibromas should be examined carefully for other evidence of neurofibromatosis.

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Year:  1998        PMID: 9587756     DOI: 10.1016/s0720-048x(97)01175-3

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


  3 in total

Review 1.  Guidelines for the diagnosis and management of individuals with neurofibromatosis 1.

Authors:  Rosalie E Ferner; Susan M Huson; Nick Thomas; Celia Moss; Harry Willshaw; D Gareth Evans; Meena Upadhyaya; Richard Towers; Michael Gleeson; Christine Steiger; Amanda Kirby
Journal:  J Med Genet       Date:  2006-11-14       Impact factor: 6.318

Review 2.  Non-ossifying fibroma, fibrous cortical defect and Jaffe-Campanacci syndrome: a biologic and clinical review.

Authors:  Henry J Mankin; Carol A Trahan; Gertrud Fondren; Carole J Mankin
Journal:  Chir Organi Mov       Date:  2009-04-29

3.  Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.

Authors:  Silvia Vannelli; Raffaele Buganza; Federica Runfola; Ilaria Mussinatto; Antonio Andreacchio; Luisa de Sanctis
Journal:  Ital J Pediatr       Date:  2020-05-11       Impact factor: 2.638

  3 in total

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