CASE REPORT
Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 261-263

An unusual oral manifestation of type 1 neurofibromatosis: A case report and review of literature


Department of Oral Medicine and Radiology, Indira Gandhi Institute of Dental Sciences, Pondicherry, India

Correspondence Address:
Dr. Vandana Shekar
Department of Oral Medicine and Radiology, Indira Gandhi Institute of Dental Sciences, Pondicherry - 607 402
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0976-9668.149225

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Neurofibroma is a benign peripheral nerve sheath tumor and is the most frequent tumor of neural origin. Its presence is one of the clinical criteria for the diagnosis of neurofibromatosis type 1 (NF1; a common hereditary disease occurring in one out of every 3000 births). The diagnosis can sometimes be made at birth, while in others the diagnosis is made later in life after the appearance of additional clinical criteria. Majority of the solitary neurofibromas are sporadic, while a few are associated with NF1 syndrome. Oral hard and soft tissue are affected by the tumor; however, the tongue is the most affected site. Gingival neurofibroma is an uncommon oral manifestation of NF. Here, we report a rare case of gingival neurofibroma in NF1 patient. One of the most feared complications of NF1 is its transformation into neurofibrosarcoma, which bears a very poor prognosis. Treatment of neurofibroma is surgical resection.


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