INTRA-OSSEOUS NEUROFIBROMA IN THE MAXILLA OF A YOUNG GIRL- A REPORT OF A RARE CASE

Cite this:
[1]
M. C. S. A. K. S. K. M. P. C. C. Vimi S Mutalik, Sunitha Carnelio, “INTRA-OSSEOUS NEUROFIBROMA IN THE MAXILLA OF A YOUNG GIRL- A REPORT OF A RARE CASE”, ijmhs, vol. 3, no. 5, Sep. 2013.
© 2022 Interactive Protocols
RIGHTS & PERMISSIONS
Article Views
403
Altmetric
1
Citations
-
LEARN ABOUT THESE METRICS
   PDF  

Abstract

The neurofibroma is a benign tumor of nerve tissue origin derived from cells that constitute the nerve sheath. It is seen as a solitary lesion or as part of a generalized syndrome of neurofibromatosis (von Recklinghausen disease of the skin). The skin is the most common site for neurofibromas. Oral lesions though found in a minority of patients with the generalized syndrome are not uncommon. The tongue and buccal mucosa are the most common sites. On rare occasions, the tumor can arise centrally within the bone. The intraosseous maxillary location is even rarer. We present a case of neurofibroma that presented in the maxilla of a young girl.

KEYWORDS:

 Special Issue

Article Metrics Graph

Chart Graph | Range Graph

Content

Section

Source

License

All paper submissions must carry the following duly signed by all the authors:
“I certify that I have participated sufficiently in the conception and design of this work and the analysis of the data (wherever applicable), as well as the writing of the manuscript, to take public responsibility for it. I believe the manuscript represents valid work. I have reviewed the final version of the manuscript and approve it for publication. Neither has the manuscript nor one with substantially similar content under my authorship been published nor is being considered for publication elsewhere, except as described in an attachment. Furthermore I attest that I shall produce the data upon which the manuscript is based for examination by the editors or their assignees, if requested.”