Juvenile ossifying fibroma in children. Problems in differential diagnosis
- Authors: Rogozhin D.V.1, Boulytcheva I.V.1
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Affiliations:
- Federal State Budget Institution Russian Children’s Clinical Hospital
- Issue: Vol 6, No 1 (2014)
- Pages: 70-73
- Section: ORTHOPAEDIC PATHOMORPHOLOGY
- Published: 27.01.2014
- URL: https://sarbon.abvpress.ru/jour/article/view/487
- ID: 487
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Abstract
Juvenile ossifying fibroma (JOF) is a group of heterogeneous benign fibro-osseous tumors of the craniofacial skeleton in young people. According to the WHO, JOF may present as one of two histologic variants: juvenile psammomatoid ossifying fibroma (JPOF) and juvenile trabecular ossifying fibroma (JTOF). Radiographycally, JOF presents as a well defined, unilocular or multilocular, expansive radiolucency with cortical thinning. The definitive diagnosis of JOF should be based on clinical and radiographic findings, in conjunction with the histopathologic characteristics of the lesion.
About the authors
D. V. Rogozhin
Federal State Budget Institution Russian Children’s Clinical Hospital
Author for correspondence.
Email: pathol.777@mail.ru
г. Москва
Russian FederationI. V. Boulytcheva
Federal State Budget Institution Russian Children’s Clinical Hospital
г. Москва
Russian FederationReferences
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