Central neurofibroma: A rare pathology at a rare site
Author(s) -
AjasA Gogri,
SonaliG Kadam,
HemantR Umarji,
P. R. Shinde
Publication year - 2014
Publication title -
journal of indian academy of oral medicine and radiology
Language(s) - English
Resource type - Journals
eISSN - 0975-1572
pISSN - 0972-1363
DOI - 10.4103/0972-1363.141866
Subject(s) - medicine , neurofibroma , neurofibromatosis , pathology , lesion , tongue , neurofibromatosis type i , oral cavity , anatomy , dentistry
Neurofibroma is a tumor of nerve tissue origin. It is an uncommon benign tumor of the oral cavity. It generally appears as a part of syndrome, neurofibromatosis type 1, i.e., Von Recklinghausen′s disease of skin. Oral neurofibroma as a solitary lesion is very uncommon. Few sporadic cases have been reported on tongue and submandibular gland. On rare occasions, the tumor can arise centrally within bone. This article presents a case of variation in the observed characteristics of neurofibroma being present centrally within maxillary alveolus and with no relation to neurofibromatosis. A discussion of its clinical, radiological, and histological features and a review of the same are included
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom