Solitary Neurofibroma of the Soft Palate: A Rare Entity.

The solitary neurofibroma is a benign tumor of neuronal origin uncommonly reported in the oral cavity. The possible association of this neoplasia with systemic pathologies, such as von Recklinghausen's disease and multiple endocrine neoplasia, makes its diagnosis fundamental. Solitary isolated neurofibroma of the soft palate not associated with von Recklinghausen's disease is an unusual tumor and probably only four cases have been reported in English literature previously. To the best of our knowledge, our case of soft palate neurofibroma in 17-year-old male represents the fifth reported in English literature, for which complete surgical excision was achieved with uneventful healing.

The position of the mental foramen in the north and south Indian populations.

OBJECTIVE: The aim of the study was to determine and compare the position of the mental foramen MF in the north and south Indian populations using Panoramic radiographs. MATERIALS AND METHODS: A total of 100 Panoramic radiographs were selected from the archives of PMNM Dental College and the Department of Oral Medicine and Radiology, of which 50 radiographs belonged to a north Indian population and 50 radiographs belonged to a local population of Bagalkot Karnataka. The position of the MF was classified into 6 positions depending on the relationship to the mandibular teeth. The distance from the superior border of the MF to the lower border of the mandible was also measured. RESULTS: The most common position of the MF was along the long axis of the second premolar in the north Indian population and in south Indian populations it was found to be between the first and second premolar. Descriptive analysis was used to compare the distance between the superior border of the mental foramen and the lower border of the mandible bilaterally. CONCLUSION: There was a significant difference in the position of the MF between the north and south Indian populations.

Acoustic Neuroma Mimicking Orofacial Pain: A Unique Case Report.

Acoustic neuroma (AN), also called vestibular schwannoma, is a tumor composed of Schwann cells that most frequently involve the vestibular division of the VII cranial nerve. The most common symptoms include orofacial pain, facial paralysis, trigeminal neuralgia, tinnitus, hearing loss, and imbalance that result from compression of cranial nerves V-IX. Symptoms of acoustic neuromas can mimic and present as temporomandibular disorder. Therefore, a thorough medical and dental history, radiographic evaluation, and properly conducted diagnostic testing are essential in differentiating odontogenic pain from pain that is nonodontogenic in nature. This article reports a rare case of a young pregnant female patient diagnosed with an acoustic neuroma located in the cerebellopontine angle that was originally treated for musculoskeletal temporomandibular joint disorder.

Hereditary ectodermal dysplasia: report of 11 patients from a family.

Hereditary Ectodermal Dysplasia is an inherited disorder commonly involving skin, teeth, hair, and nails. We have observed ectodermal dysplasia (EDs) in 11 individuals over two generations in one family. Smooth, dry, thin skin was seen in most affected individuals. All had fine, slow-growing scalp hair and body hair and some had sparse eyebrows and short eyelashes. Nearly all showed decrease in sweating. Severe teeth abnormalities were seen in all patients and fingernail abnormalities were not so severe but toenail abnormalities were seen in all patients. No other abnormalities were seen in affected individuals in this family. It is very rare to find such a large family having ectodermal dysplasia.