DMFR
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hisatomi, M
Right arrow Articles by Kishi, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hisatomi, M
Right arrow Articles by Kishi, K
Dentomaxillofacial Radiology (2005) 34, 380-383
© 2005 British Institute of Radiology
doi: 10.1259/dmfr/46427075


CASE REPORT

Bone deformity showing a deep coronoid notch of the mandible in a patient with neurofibromatosis type 1

M Hisatomi*, J Asaumi, H Konouchi, Y Yanagi and K Kishi

Department of Oral and Maxillofacial Radiology, Field of Tumor Biology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan

*Correspondence to: Miki Hisatomi, Department of Oral and Maxillofacial Radiology, Field of Tumor Biology, Graduate School of Medicine and Dentistry, Okayama University, 2-5-1, Shikata-cho, Okayama-city, Okayama, 700-8525, Japan; E-mail: tomi{at}md.okayama-u.ac.jp

Received 2 December 2004; revised 8 March 2005; accepted 17 April 2005

We present a case of a 10-year-old girl with neurofibromatosis type 1 related skeletal dysplasia. In the present case, a unilocular radiolucency at the left coronoid notch visible on a panoramic radiograph was suspected to be a neurofibroma. However, only the presence of bone deformities was observed on CT. Fat-like tissue adjacent to the bone deformities inside the left mandibular ramus was revealed, and the presence of neurofibroma was unequivocally denied on the MR images. However, biopsy of the lesion suggested neurofibroma. The diagnostic imaging 18 months after the first visit did not revealed a tumourous mass. However, careful follow up is required even though we could not prove the presence the lesion on the basis of imaging.

Keywords: neurofibromatosis type 1; Von Recklinghausen's disease; mandibular foramen; neurofibroma




This article has been cited by other articles:


Home page
Dentomaxillofac RadiolHome page
Z J Sun, Y F Zhao, S P Wang, and S G He
Giant facial haematoma in neurofibromatosis type 1
Dentomaxillofac. Radiol., January 1, 2008; 37(1): 52 - 57.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
BJR DMFR IMAGING ALL BIR JOURNALS
Copyright © 2005 by the British Institute of Radiology.