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Published in: MUSCULOSKELETAL SURGERY 1/2009

01-05-2009 | Original Article

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

Published in: MUSCULOSKELETAL SURGERY | Issue 1/2009

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Abstract

Non-ossifying fibroma of bone (NOF) is a common entity, more frequently found in male children and consisting of a solitary eccentric, lytic expanded lesion in the metaphysis of a long bone. The disorder is benign and most often asymptomatic but may result in a fracture requiring therapy. Of some importance is to distinguish NOF from another very similar but smaller lesion, fibrous cortical defect, which is almost always asymptomatic and eccentrically located. Even more striking is a very rarely encountered lesion known as Jaffe–Campanacci syndrome, which also occurs in children who present with typical non-ossifying fibromatous tumors but in multiple sites. In addition, these patients have some systemic and dermal findings resembling those seen in patients with Type 1 neurofibromatosis.
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Metadata
Title
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
Publication date
01-05-2009
Publisher
Springer Milan
Published in
MUSCULOSKELETAL SURGERY / Issue 1/2009
Print ISSN: 2035-5106
Electronic ISSN: 2035-5114
DOI
https://doi.org/10.1007/s12306-009-0016-4

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