Juvenile Ossifying Fibroma - WHO Type

Journal Title: Journal of Case Reports and Studies - Year 2014, Vol 2, Issue 2

Abstract

Juvenile ossifying fibroma is an uncommon clinical entity, its aggressive local behaviour and high recurrence rate mean that it is important to make an early diagnosis, apply the appropriate treatment and, especially, follow the patient up over the long term. In the current article we report a case of juvenile ossifying fibroma-WHO type in 12yr old patient which was clinical and histopathologically challenging as it was asymptomatic and at an unusual location.

Authors and Affiliations

Rathore AS

Keywords

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  • EP ID EP582456
  • DOI 10.15744/2348-9820.1.502
  • Views 123
  • Downloads 0

How To Cite

Rathore AS (2014). Juvenile Ossifying Fibroma - WHO Type. Journal of Case Reports and Studies, 2(2), 1-4. https://europub.co.uk./articles/-A-582456